![]() Non-peptidyl inhibitors of vla-4 dependent cell binding useful in treating inflammatory, autoimmune,
专利摘要:
The present invention relates to species of non-peptide-based compounds, which are useful VLA-4 inhibitors for the treatment of inflammatory, autoimmune and respiratory diseases and which comprise a compound of formula 1.0.0 and pharmaceutically acceptable salts and other prodrug derivatives thereof It is about. Formula 1.0.0 Where A is (C 1 -C 6 ) alkyl, cycloalkyl, aryl, heteroaryl or heterocyclyl [these radicals are as defined herein and the radical alkyl, cycloalkyl, aryl, heteroaryl or heterocyclyl Optionally substituted with 0 to 3 substituents identical to R 9 , defined below; or A 1 -NHC (= 0) NH-A 2- , A 1 -NHC (= 0) OA 2- , A 1- OC (= O) NH-A 2- , A 1 -NHSO 2 NH-A 2- , A 1 -NHC (= O) -A 2- , A 1 -C (= O) NH-A 2- , A 1 -NHSO 2 -A 2- , A 1 -SO 2 NH-A 2- , A 1- (CH 2 ) r -A 2- , A 1 -CH (R 1 ) -OA 2- , A 1- ( CH 2 ) r OA 2- , A 1 -O (CH 2 ) r -A 2- , A 1- (CH 2 ) r NH-A 2- , A 1 -NH (CH 2 ) r -A 2- , And A 1- (CH 2 ) r S (= 0) q -A 2- , wherein A 1 and A 2 are each independently hydrogen, aryl, (C 1 -C 6 ) alkyl, (C 2 -C 6 ) Alkenyl, (C 2 -C 6 ) alkynyl, cycloalkyl, heteroaryl and heterocyclyl, wherein said aryl, alkyl, cycloalkyl, Heteroaryl or heterocyclyl group is a component selected from the group consisting of radicals of 0 to 3 substituents equal to R 9 defined below; B is a component independently selected from the group consisting of residues of the partial formulas 1.1.0 to 1.1.23; E is a single bond; -O-; -NR 10- , -CH = CH-, -C≡C-; -S (= 0) q- ; -CR 11 R 12 NR 10- ; Or -CR 11 R 12- ; X is -O-; -C (= 0)-; -S (= 0) q- ; Or -NR 10- ; X 1 , X 2 and X 3 are each independently CH; CR 9 ; And N; Y is a single bond; -C (= 0)-; -C (= S)-; Or -S (= 0) 2- ; k is an integer independently selected from 0, 1 and 2; m is an integer independently selected from 0 and 1; n is an integer independently selected from 0, 1 and 2; p is independently an integer of 0 or 1 and should be selected to 1 when B is selected as a residue of partial formula 1.1.0 to 1.1.11; q is an integer independently selected from 0, 1 and 2; r is an integer independently selected from 0, 1 and 2; R 1 is (C 1 -C 3 ) alkyl substituted with 0 or 1 F; CF 3 ; OCF 3 ; Or cyano; R 2 and R 3 are each independently hydrogen; A (C 1 -C 6) alkyl, optionally substituted by R 13 and the same 0 to 3 substituents as defined below (C 2 -C 6) optionally substituted with R 13 to define with the same 0 to 3 substituents alkenyl, defined below substituted with the same 0 to 3 substituents, and R 13 is (C 3 -C 14) carbocyclic ring system, the following definitions and R 13 is substituted by 0 to 3 substituents the same The same heterocyclyl ring as defined herein, substituted with (C 1 -C 6 ) alkyl-OR 5 , substituted with 0 to 3 substituents identical to R 13 as defined below, 0 to 3 R 13 (C 1 -C 6 ) alkyl-SR 5 , (C 1 -C 6 ) alkyl-SO 2 R 5 , 0 to 3 R substituted by 0 to 3 substituents the same as R 13 defined below 13 is substituted the same 0 and R 13 is the same heteroaryl ring, and to define as defined herein Which it is substituted by three substituents, and are each independently selected from the group consisting of the same aryl ring as defined herein; Provided that R 2 and R 3 are each the same as defined above; Together they form a ring as defined below; One of which together with R 4 forms a group as defined below in which case the other is hydrogen or methyl; R 2 and R 3 together form a cycloalkyl or heterocyclyl ring substituted by 0 to 3 substituents same as R 13 , defined below; R 2 or R 3 is the same heteroaryl or heterocyclyl as defined herein and substituted by R 4 , and 0 to 3 substituents identical to R 13 , defined below, together with the carbon and nitrogen atoms to which they are attached, respectively; To form a group; R 4 is hydrogen; Or (C 1 -C 6 ) alkyl optionally substituted by the same substituent R 13 as defined below, or R 4 together with R 2 or R 3 form a carbocyclic or heterocyclic ring; R 5 and R 6 are independently hydrogen; Or (C 1 -C 6 ) alkyl; (C 2 -C 6 ) alkenyl; (C 2 -C 6 ) alkynyl; CF 3 ; Aryl; Cycloalkyl; Heteroaryl; Or heterocyclyl, wherein the alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heteroaryl or heterocyclyl is substituted by 0 to 3 substituents equal to R 13 defined below; R 7 is (C 1 -C 6 ) alkyl; (CH 2 ) k OR 5 ; (CH 2 ) k C (= 0) R 5 ; (CH 2 ) k C (= 0) NR 6 R 5 ; (CH 2 ) k NR 6 C (= 0) R 5 ; (CH 2 ) k NR 6 C (= 0) OR 5 ; (CH 2 ) k NR 6 SO 2 R 5 ; (CH 2 ) k NR 6 R 5 ; F; CF 3 ; OCF 3 ; Aryl substituted with 0 to 3 substituents identical to R 9 defined below; Heterocyclic substituted by 0 to 3 substituents equal to R 9 defined below; Heteroaryl substituted by 0 to 3 substituents the same as R 9 defined below; Or cycloalkyl substituted by 0 to 3 substituents equal to R 9 defined below; R 7 may form a cycloalkyl or heterocyclic ring with R 8 ; R 7 may form a cycloalkyl or heterocyclyl ring with R 11 ; R 8 is hydrogen; F; CN; (C 1 -C 6 ) alkyl or (C 1 -C 6 ) alkoxy; R 9 is hydrogen; (C 1 -C 6 ) alkyl; (C 1 -C 6 ) alkoxy; (C 3 -C 6 ) cycloalkyl; (C 3 -C 6 ) cycloalkoxy; Cyano; (CH 2 ) k OH; C (= 0) R 5 ; (CH 2 ) k C (O) NR 5 R 6 ; (CH 2 ) k NR 6 SO 2 R 5 ; CF 3 ; OCF 3 ; SO 2 NR 5 R 6 ; Or (CH 2 ) m C (= 0) OR 5 ; When R 9 is bonded to a saturated carbon atom R 9 may be = O or = S; R 9 may be ═O when R 9 is bonded to a sulfur atom; R 10 is hydrogen; C (= 0) R 5 ; C (= 0) OR 5 ; (C 1 -C 6 ) alkyl; Aryl; Heterocyclyl; Heteroaryl; Cycloalkyl; Or SO 2 R 5 ; R 11 and R 12 are independently -H; (C 1 -C 6 ) alkyl; -OH; -CN; (C 1 -C 6 ) alkoxy; NR 6 C (= 0) R 5 ; NR 6 SO 2 R 5 ; NR 6 R 5 ; CF 3 ; F; Aryl; Heterocyclyl; Heteroaryl; Cycloalkyl; Or cycloalkoxy; R 11 may form a cycloalkyl or heterocyclic ring with R 12 ; R 13 is halogen; CF 3 ; (C 1 -C 6 ) alkyl; Aryl; Heteroaryl; Heterocyclyl; Hydroxy; Cyano; (C 1 -C 6 ) alkoxy; (C 3 -C 6 ) cycloalkyl; (C 3 -C 6 ) cycloalkoxy; (C 2 -C 6 ) alkynyl; (C 2 -C 6 ) alkenyl; -NR 6 R 5 ; -C (= 0) NR 5 R 6 ; SO 2 R 5 ; C (= 0) R 5 ; NR 5 SO 2 R 6 ; NR 5 C (= 0) R 6 ; C (= 0) NR 5 SO 2 R 6 ; NR 5 C (= 0) OR 6 ; And SO 2 NR 6 R 5 . Chemical Formula 1.1.0 Formula 1.1.1 Formula 1.1.2 Formula 1.1.3 Chemical Formula 1.1.4 Formula 1.1.5 Formula 1.1.6 Chemical Formula 1.1.7 Chemical Formula 1.1.8 Formula 1.1.9 Formula 1.1.10 Formula 1.1.11 Formula 1.1.12 Formula 1.1.13 Formula 1.1.14 Formula 1.1.15 Formula 1.1.16 Formula 1.1.17 Formula 1.1.18 Formula 1.1.19 Formula 1.1.20 Formula 1.1.21 Formula 1.1.22 Formula 1.1.23 Where The indication of "*" indicates the point at which the moiety of each partial formula 1.1.0 to 1.1.23 binds to the residue "CR 2 R 3 " of formula 1.0.0, The indication of "→" indicates the point at which the moiety of each partial formula 1.1.0 to 1.1.23 binds to the residue "E" of formula 1.0.0, Residues of each partial formula 1.1.0 to 1.1.23 may be optionally substituted with R 9 except for the residues of partial formula 1.1.10, 1.1.17 and 1.1.23. 公开号:KR20020067050A 申请号:KR1020027008400 申请日:2000-12-15 公开日:2002-08-21 发明作者:추파크루이스스탠리;두플란티어알렌야콥;라우완팡;밀리치안토니존 申请人:화이자 프로덕츠 인코포레이티드; IPC主号:
专利说明:
NON-PEPTIDYL INHIBITORS OF VLA-4 DEPENDENT CELL BINDING USEFUL IN TREATING INFLAMMATORY, AUTOIMMUNE, AND RESPIRATORY DISEASES} [2] One of the most basic methods required for normal host protection is the controlled introduction of leukocytes from the vasculature. The system is designed to allow normal recirculation of leukocytes, but this allows for the rapid outflow of leukocytes from the damaged area, which is one of the central pathogenesis of inflammatory, respiratory and autoimmune diseases in mammals. Cell adhesion is a major factor in this process and it is particularly relevant to the present invention with respect to cell / cell and cell / matrix binding of VLA-4 containing hematopoietic cells. [3] VLA-4 is a member of the superfamily of cell surface macromolecular receptors, the so-called integrins, which are non-covalent heterodimeric complexes composed of α subunits and β subunits (Hemler, Ann. Rev. Immunol. , 8, p. 365, 1990]. 18 different α subunits were identified and classified as α 1 -α 10 , α L , α M , α X , α D , α LRI , α IIB , α V and α E ; Eight different β subunits were identified and classified as β 1 -β 8 . Each integrin molecule can be classified into a superfamily based on the type of its α and β subunits. [4] α 4 β 1 integrin, VLA-4, is an integrin expressed in all leukocytes (eg, monocytes, lymphocytes, basophils, eosinophils, breast cells, and macrophages) except constitutive polymorphonuclear leukocytes. Binding of this integrin to one of its ligands has many known cellular adhesion and activation functions (Hemler, Ann. Rev. Immunol., 8, p.365, 1990; Walsh et al., Clin. And Exp. Allergy, 25, p. 1128, 1995; Huhtala et al., J. Cell Biol., 129, p.867, 1995]. In particular, it is an alternatively conjugated form of the CS-1 domain containing extracellular matrix protein fibronectin (FN) (Ruegg et al., J. Cell Biol., 177, p. 179, 1991; Wayner et al., J. Cell Biol., 105, p. 1873, 1987; Kramer et al., J. Biol. Chem., 264, p.4684, 1989; Gehlsen et al., Science, 24, p. 1228, 1988). Or cytokines known as vascular cell adhesion molecule-1 (VCAM-1) for the extracellular matrix protein osteopontin (Bayless, KI et al. J. Cell Science, 111, p. 1165-1174, 1998). It is a receptor for inducible endothelial cell surface proteins. The importance of VLA-4 cell adhesion interactions was established by the use of specific monoclonal antibody (mAb) antagonists of the α subunit of VLA-4, and inflammatory, respiratory or autoimmune pathologies with many inhibitors of VLA-4 dependent cells. Preventing or inhibiting the condition is illustrated (Chisholm et al., Eur. J. Immunol., 23, p.682, 1993; Lobb et al., J. Clin. Invest., 94, p.1722, 1994; Richards et al., Am. J. Respir. Cell Mol. Biol., 15, p. 172, 1996; Soiluhanninen et al., J. Neuroimmunol., 72, p. 95, 1997; Sagara et al., Int. Arch. Allergy Immulogy., 112, p. 287, 1997; Fryer et al., J. Clin. Invest., 99, p. 2036, 1997). In addition, confirmation that these pathological processes can be inhibited by agents other than antibodies has been observed in animal models receiving treatment with small molecule peptide inhibitors of VLA-4 or synthetic CS-1 peptides (Ferguson et al., Proc. Natl. Acad, Sci., 88, p. 8072, 1991; Wahl et al., J. Clin. Invest., 94, p.655, 1994; Molossi et al., J. Clin. Invest., 95 , p. 2601, 1995; Abraham et al., Am. J. Respir. Crit. Care Med., 156, p. 696, 1997; Jackson et al., J. Med. Chem., 40, p. 3359, 1997]). [5] Description of the technical state [6] Studies on mAb and peptide VLA-4 antagonists in the art have already been shown above. In defining the binding site for α 4 β 1 , we observed that lymphocytes can bind to two different sites on fibronectin (Bernardi et al., J. Cell Biol., 105, p. 489, 1987]). One component of this cell binding activity was previously identified as tripeptide Arg-Gly-Asp (RGD) that binds to integrin α 5 β 1 (VLA5). Subsequently, the minimum amino acid sequence required to bind and antagonize the activity of VLA-4 on leukocytes on alternatively conjugated sites in fibronectin was determined (Humphires et al., J. Biol. Chem., 266). , p. 6886, 1987; Garcia-Pardo et al., J. Immunol., 144, p.3361, 1990; Komoriya et al., J. Biol. Chem., 266, p.15075, 1991). Pentapeptides with two overlapping pentapeptides in the CS-1 region of fibronectin (FN): Gl-Ile-Leu-Asp-Val and Leu-Asp-Val-Pro-Ser as well as octapeptides: Glu-Ile It was found to contain -Leu-Asp-Val-Pro-Ser-Thr. Both of these peptides inhibit FN-dependent cell adhesion and reach the previous conclusion that the minimum amino acid sequence required for inhibition is Leu-Asp-Val (LDV). Indeed, LDV minimal inhibitory sequences have been observed to be equally effective as full length CS-1 fragments when binding activated forms of VLA-4 (Wayner et al., J. Cell Biol., 116, p. 489, 1992). [7] Various integrins are thought to bind to extracellular matrix proteins at Arg-Gly-Asp (RGD) recognition sites. For α 4 β 1, the primary recognition site on FN is LDV, but an RGD-based cyclic peptide is known that can inhibit both α 4 β 1 and α 5 β 1 binding to FN. The cyclic peptide may be of Formula 0.0.1. [8] [9] Where [10] TPro stands for 4-thioproline. [11] Other peptidyl inhibitors of VLA-4 are assigned to Cytel Corporation and are disclosed in International Patent Publication Nos. WO95 / 15973 to Arrhenius et al. In US Pat. Nos. 5821231 and 5936065 ("CS"). -1 Peptidomimetics "). Representative compounds of the type described are peptides of the formula 0.0.2 (International Patent Publications WO95 / 15973, US Pat. Nos. 5821231 and 5936065; Cytel Corporation). [12] N-phenylacetyl-Leu-Asp-Phe-NCy 3 [13] Where [14] NCy 3 is especially morpholine amido; Thiomorpholine amido; 4- (thiadioxo) piperidineamido; And D-2- (carboxamide) -pyrrolidineamido; Piperidineamido; And substituted piperidineamido. [15] Further work by Arenius et al. On the cyclic CS-1 peptidomimetics is described in International Patent Publication No. WO96 / 06108 assigned to Cytel Corporation in connection with US Pat. No. 5869448 (International Publication No. WO96 / 06108; Cytel Corporation). [16] The Arrhenius group also found nonpeptidal inhibitors of VLA-4 dependent cell binding described in He et al. International Patent Publication No. WO98 / 42656. Inhibitors described herein are compounds of Formula 0.0.3. [17] [18] Typical inhibitors are compounds of formula 0.0.4 (WO 98/42656; Cytel Corporation). [19] [20] Leu-Asp-Val tripeptide is an inhibitor of the VLA-4 dependent cell adhesion described in WO96 / 22966, published by Adams et al., Assigned to Biogen, Inc. It is used as the center of the group. These inhibitors can be represented by compounds of the formula 0.0.5 [21] [22] Where [23] R 1 may be 4- (N '-(2-methylphenyl) urea) phenylmethyl; [24] Y may be C═O; [25] R 2 may be H; [26] R 3 may be iso-butyl; [27] R 14 may be 1,3-benzodioxol-5-yl. An example of a typical inhibitor of this type is a compound of the formula 0.0.6 (International Patent Publication WO96 / 22966; Biogen Incorporated). [28] [29] The Adams group also found semipeptide cell adhesion inhibitors for the treatment of inflammatory and autoimmune diseases described in Lin et al., WO97 / 03094. Such inhibitors can be represented by compounds of the formula 0.0.7 (WO97 / 03094; Biogen Incorporated). [30] Z- (Y 1 )-(Y 2 )-(Y 3 ) n -X [31] Where [32] Z can be 4- (N '-(2-methylphenyl) urea) phenylacetyl; [33] (Y 1 )-(Y 2 )-(Y 3 ) n represents a series of amino acids forming a peptide chain; [34] X may be OH. Typical inhibitors of this type are represented by the formula 0.0.8. [35] [36] The Adams group also found that, in Zheng et al. International Patent Publication No. WO98 / 04247 (Biogen Inc.), existing IIB / IIIa integrin inhibitory compounds can be converted to VLA-4 inhibitory compounds and IIb / IIIa It was found that inhibitory compounds can be prepared by binding specific VLA-4 integrin backbones with IIb / IIIa specificity determinants. These cell adhesion inhibitors include compounds of Formula AB, wherein A is a VLA-4 specific determinant that does not confer significant IIb / IIIa integrin inhibitory activity; B is an integrin skeleton derived from IIb / IIIa inhibitors. Can be seen. Also described is a three-dimensional pharmacodynamic model of compounds with VLA-4 inhibitory activity. Examples of inhibitors so induced are compounds of the formulas 0.0.9 and 0.0.10 (International Patent Publication No. WO98 / 04247; Biogen Incorporated). [37] [38] [39] International patent publication WO98 of Singh et al., Relating to a three-dimensional drug action generating stage of a compound having a VLA-4 inhibitory activity, comprising the characteristics defined by the tables of resistance and three-dimensional ligands x, y and z. See / 04913. The following compound, which is an example of the compound mentioned, may be a compound of the formula 0.0.11 (International Publication No. WO98 / 04913; Biogen Incorporated). [40] [41] Another type of VLA-4 dependent cell adhesion inhibitor is described in WO 98/54207 ("Anti-inflammatory Tyrosine Derivatives") of Head et al. And may be a compound of formula 0.0.12 . Typical compounds of this type of inhibitor may be compounds of the formula 0.0.13 (International Publication No. WO98 / 54207; Celltech Therapeutics Ltd.). [42] [43] Where [44] R 1 is an optionally substituted alkyl or aromatic group; [45] X 2 is —C (═O) —; -C (= 0) O-; -C (= 0) NH-; Or -S (= 0) 2- ; [46] R 7 is an optionally substituted alkyl or aryl group. [47] [48] The head group also found a related group of VLA-4 dependent cell adhesion inhibitors described in Head et al. WO99 / 37618 ("Phenylalanine Deritivatives Useful As Pharmaceutical Agents"), which are compounds of the formula 0.0.14 to be. [49] [50] Where [51] L 1 is a bridging atom or group; [52] A is chain-[C (R 7 ) (R 8 )] p -Y- [C (R 9 ) (R 10 )] q- ; [53] L 2 is -C (= 0)-; -C (= 0) O-; -C (= S)-; -S (= 0) 2 -or -C (= 0) N (R 11 )-. An example of this type of inhibitor is a compound of the formula 0.0.15 (International Publication No. WO99 / 35163; Celtech Thermopetics Limited). [54] [55] Another closely related group of VLA-4 inhibitors found by the head group is described in International Patent Publication No. WO99 / 37618 to Head et al. ("Novel Phenylalanine Derivatives Useful as Integrin Antagonists"), characterized by the following formula 0.0.16 It is done. [56] [57] Representative examples of such inhibitory compounds are compounds of the formula 0.0.17 (WO 99/37618; Celtech Thermopetics Limited). [58] [59] A further related group of compounds found by the head group as inhibitors of VLA-4 dependent cell adhesion are described in WO99 / 43642 ("Phenylalanine Derivatives As Inhibitors of Alpha4 Integrins"), which is represented by the following formula 0.0. It is characterized by 18. [60] [61] Inhibitors of the type described are represented by the formula 0.0.19 (International Patent Publication No. WO99 / 43642; Celtech Thermopetics Limited). [62] [63] Previous studies in the discovery of inhibitors of VLA-4 dependent cell adhesion have also been described, for example, in International Patent Publication No. WO96 to Thorsett et al., Assigned to Athena Neurosciences, Inc. And Pleiss and their collaborators, as described in / 01544 ("Inhibitors of Leukocyte Adhesion"). Such inhibitors include inhibitors that block cell adhesion mediated by VLA-4 and they are used to treat a number of inflammatory diseases, particularly inflammatory brain disorders. [64] Non-peptides, ie small molecule inhibitors of VLA-4, may also be used in Tocet's International Patent Publication No. WO99 / 06390 (“Carbamoyloxy Compounds Which Inhibit Leukocyte Adhesion Mediated by VLA-4”) assigned to Athena Neurosciences Incorporated. By place and toset groups as described in. Inhibitors of this type may be compounds of the formula 0.0.20 [65] [66] Where [67] R 1 is alkyl, aryl, cycloalkyl, heterocyclic or heteroaryl, all of which may be optionally substituted; [68] R 2 is defined similarly to R 1, and R 1 and -S (= O) 2 - in combination with residues may form a cyclic three interrogating optionally substituted; [69] R 3 is defined similarly to R 1 and optionally may form an optionally substituted heterocyclic group together with the nitrogen bonded to R 2 and the carbon atom bonded to R 3 ; [70] R 7 is -H or alkyl; [71] Ar is optionally substituted aryl or heteroaryl; [72] R 5 ' is -OZ-NR 8 R 8' or -OZR 12 ; [73] Z is -C (= 0)-or -S (= 0) 2 ; [74] R 8 and R 8 ' are -H or optionally substituted alkyl, cycloalkyl or heterocyclic or R 8 and R 8' can be joined to form an optionally substituted heterocyclic; [75] R 12 is optionally substituted heterocycle. [76] Representative examples of such VLA-4 inhibitors are compounds of formula 0.0.21 (WO99 / 06390; Athena Neurosciences, Inc.). [77] [78] Binding of α-9 integrins to Yednock and Place International Patent Publication No. WO99 / 06391 ("Alpha-9 Integrin Antagonists and Anti-inflammatory Compositions") assigned to Athena Neurosciences Inc. The use of the inhibitory compounds of the above-mentioned International Patent Publication No. WO 99/06390, in particular, in the treatment of disorders comprising adherent macrophages or neutrophils. Treatment-sensitive disorders include airway overreaction and obstruction with chronic asthma, smooth muscle cell proliferation in atherosclerosis, vascular obstruction after angioplasty, fibrosis and glomerular scar as a result of kidney disease, aortic stenosis, rheumatoid arthritis Hypertrophy of the synovial membrane, and scars and Crohn's disease following the progression of ulcerative colitis. [79] The Tosset and Place Group is a member of the International Patent Publication No. WO99 / 06431 ("Substituted Phenylalanine Type Compounds Which Inhibit Leukocyte, such as Tosette, which was assigned to Athena Neurosciences Inc. and American Home Products Corporation). Adhesion Mediated by VLA-4 ") has found a group of inhibitors of VLA-4, which can be represented by the following formula 0.0.22. [80] [81] Where [82] R 1 , R 2 , R 3 , R 7 and Ar have substantially the same meanings as described in WO 99/06390; [83] R 5 is —NHC (═O) R; Alkoxyaryl; Aryl; Heteroaryl; -NRR '; Alkoxy-NRR ';Alkenyl;Alkenyl;Aryloxy;Heteroaryloxy;Alkoxy-heterocyclic;O-heterocyclic;Tetrazolyl; -NRS (= 0) 2 -alkyl; Alkenylsulfonylamino; Alkynylsulfonylamino; Alkoxy; Amidine; -C (= 0) NRR '; -NRC (= 0) R '; S (= 0) 2 -aryl; S (= 0) 2 -heteroaryl; -NRC (= 0) NRR '; -NRC (= 0) OR '; Aminocarbonyl (N-formylheterocyclyl); And alkyl-C (= 0) NH-heterocyclyl. [84] Compounds exemplifying the types of VLA-4 inhibitors disclosed are compounds of formula 0.0.23 (WO 99/06431; Athena Neurosciences, Inc.). [85] [86] The related group of inhibitor compounds found by the toset and place groups are also described in Tosett International Patent Publication No. WO99 / 06432 ("Dipeptide and Related Compounds") assigned to Athena Neurosciences Incorporated and American Home Products Corporation. Which Inhibit Leukocyte Adhesion Mediated by VLA-4 "). Inhibitory compounds of this type are characterized by the following formula 0.0.24. [87] [88] Where [89] R 1 , R 2 , R 3 and R 7 have substantially the same meanings as described in WO 99/06390 and WO 99/06431; [90] R 5 is -ALK-X- or = CH-Y; [91] X and Y are both defined to mean various groups that may be optionally substituted. [92] An example of this type of VLA-4 inhibitor is a compound of formula 0.0.25 (International Publication No. WO99 / 06432; Athena Neurosciences Inc.). [93] [94] Further related groups of VLA-4 inhibitory compounds found by the toset and place groups are also described in International Patent Publication No. WO99 /, such as Dappen, assigned to Athena Neurosciences Inc. and American Home Products Corporation. 06433 ("Compounds Which Inhibit Leukocyte Adhesion Mediated by VLA-4"). Inhibitory compounds of this type are characterized by the following formula 0.0.26. [95] [96] Where [97] R 1 , R 2 , R 3 and R 7 have substantially the same meanings as described in WO 99/06390, WO 99/06431 and WO 99/06432; [98] X is -H; -OH; Acylamino; -C (= 0) OH; And optionally substituted alkyl; Alkoxy; Aryl; Aryloxy; Aryloxyaryl; Carboxy-alkyl; Carboxy-cycloalkyl; Carboxy-aryl; Carboxy-heteroaryl; Carboxy-heterocyclic; And cycloalkyl. [99] VLA-4 inhibitors of the type described in the preceding paragraph are characterized in that they are compounds of the formula 0.0.27 (WO 99/06433; Athena Neurosciences Incorporated). [100] [101] A further group of VLA-4 inhibitory compounds found by the tocet and place groups are International Patent Publication No. WO99 / 06434 to Ashwell et al. Assigned to Athena Neurosciences Inc. and American Home Products Corporation. No. "4-Amino-Phenylalanine Type Compound Which Inhibit Leukocyte Adhesion Mediated by VLA-4". Inhibitory compounds of this type are characterized by the following formula 0.0.28. [102] [103] Where [104] R 1 , R 2 , R 3 and R 7 have substantially the same meanings as described in WO 99/06390, WO 99/06431, WO 99/06432 and WO 99/06433; [105] R is -H, alkyl or aryl; [106] X is O, S or NR; [107] Y is NRR 'or heterocycle, all of which are optionally substituted with various groups. [108] This additional type of VLA-4 inhibitor can be exemplified by the compound of formula 0.0.29 (WO 99/06434, Athena Neurosciences, Inc.). [109] [110] Other groups of VLA-4 inhibitors structurally related to this group of VLA-4 inhibitors described above, discovered by the Tocet and Place group, include Toset et al. Assigned to Athena Neurosciences Inc. and American Home Products Corporation. International Patent Publication No. WO99 / 06435 ("Dipeptide Compounds Which Inhibit Leukocyte Adhesion Mediated by VLA-4"). Inhibitory compounds of this type are characterized by the following formula 0.0.30. [111] [112] Where [113] R 1 , R 2 , R 3 and R 7 are substantially the same as those described in International Patent Publication Nos. WO99 / 06390, WO99 / 06431, WO99 / 06432, WO99 / 06433 and WO99 / 06434. Have the same meaning; [114] R 5 has substantially the same meaning as described in WO 99/06432; [115] R 4 is -H; And optionally substituted alkyl; Cycloalkyl; Aryl; Heteroaryl; Heterocyclic; [116] R 1 and R 2 may be together or R 2 and R 3 together or R 3 and R 4 together may form a cycloalkyl or heterocyclic group. [117] This type of VLA-4 inhibitor may be a compound of formula 0.0.31 (WO 99/06435; Athena Neurosciences Inc.). [118] [119] A further group of structurally related inhibitors of VLA-4 dependent cell adhesion discovered by the toset and place groups are international patent publications such as Toset et al. Assigned to Athena Neurosciences Inc. and American Home Products Corporation. WO 99/06436 ("Benzyl Compounds Which Inhibit Leukocyte Adhesion Mediated by VLA-4"). Inhibitory compounds of this type are characterized by the following formula 0.0.32. [120] [121] Where [122] R 1 , R 2 , R 3 and R 7 are substantially the same as those described in International Patent Publication Nos. WO99 / 06390, WO99 / 06431, WO99 / 06432, WO99 / 06433 and WO99 / 06434. Have the same meaning; [123] Ar is aryl or heteroaryl. This type of VLA-4 inhibitor may be a compound of formula 0.0.33 (WO 99/06436; Athena Neurosciences). [124] [125] International patent publications WO99 / 06390, WO99 / 06431, WO99 / 06432, WO99 / 06433, WO99 / 06434, WO99 /, except as distinguished from these by broad clues. There are further descriptions of the compounds structurally related to those described in 06435 and WO99 / 06436, ie, in the International Patent Publication No. WO99 / 06437 to Tocet et al. (“Sulfonylated Dipeptide Compounds Which Inhibit Leukocyte Adhesion Mediated by VLA”). -4 "). Three such inhibitory compounds are compounds of the formulas 0.0.34 to 0.0.36 (International Publication No. WO99 / 06437; Athena Neurosciences Incorporated). [126] [127] [128] [129] The Stillz and Wehner groups have discovered different classes of compounds that have inhibitory activity on VLA-4 mediated cell adhesion. Such inhibitory compounds are described, for example, in European Patent No. 842 943 ("5-Ring Heterocycles As Inhibitors of Leukocyte Adhesion and As VLA-4 Antagonists") assigned to Hoechst AG, It is characterized in that the formula 0.0.37. [130] [131] Where [132] R is 4-amino-phenyl, 4-guanidino-phenyl, 4-aminomethyl-phenyl, 3-amino-propyl or 3-guanidino-propyl; [133] R 1 is methyl or benzyl; [134] R 2 is —H, methyl, ethyl, optionally substituted benzyl or naphthylmethyl; [135] R 3 is a mono-, di- or tri-peptide; [136] R 4 is -H, methyl or butyl; [137] R 5 is —H, alkyl, cycloalkyl or optionally substituted aryl. Representative compounds within the class of this class of VLA-4 inhibitors are compounds of formula 0.0.38 (European Patent No. 842 943; Hoechst AG). [138] [139] The Steeles and Wenner Group are also structurally close to the compounds of European Patent No. 842 943 and described in European Patent No. 842 944 ("Heterocycles As Inhibitors of Leukocyte Adhesion and As Antagonists of VLA-4"). Inhibitory compounds were found. These compounds may be characterized by the following formula 0.0.39. [140] [141] Where [142] R 4 is methyl, 4-R 3 -phenyl, wherein R 3 is 4,5-dihydroimidazol-2-yl or -C (= 0) NH 2 ; [143] R 2 is optionally substituted phenyl, pyridyl or naphthyl; [144] R 4 is -H, ethyl, n-butyl or iso-butyl. Representative examples of this type of compound are compounds of the formula 0.0.40 (European Patent No. 842 944; Hoechst AG). [145] [146] Further inhibitory compounds that are structurally close to the compounds of EP 842 944 are described in Stilts et al. EP 842 945, which can be characterized by the formula 0.0.41. [147] [148] Where [149] R is 4-R 2 -phenyl, wherein R 2 is —CN, —NO 2 , optionally substituted —NH 2 C (═O) NH or —NH 2 C (═O) NHCH 2 ; [150] R 2 is optionally substituted phenyl. Representative examples of this type of inhibitor are compounds of the formula 0.0.42 (European Patent No. 842 945; Hoechst AG). [151] [152] The Stills and Wenner Group also found that European Patent No. 903 353 (“Imidazolidine Derivatives with VLA-4 Antagonist Activity Useful for the Treatment of Diseases”, assigned to Hoechst Marion Roussel Deutschland GmBH). Inhibitors of VLA-4 dependent cell adhesion described in Mediated by Leukocyte Adhesion ". Compounds of this type are characterized by the following formula 0.0.43. [153] [154] Where [155] A is optionally substituted alkylene, alkenylene, phenylene, -phenyl-alkylene or alkylene-phenyl-; [156] L and M are a bond or CH 2- ; [157] X is optionally substituted -CH (R 7 )-or -C (= CHR 7 )-, wherein R 7 is optionally substituted alkyl, phenyl, furyl, thienyl, pyrrolyl, indazolyl or pyridinyl )ego; [158] R 1 is —H, cycloalkyl, optionally substituted alkyl, aryl, heterocyclyl; -C (= 0) R 6 or -SOR 6 , wherein R 6 is -H, cycloalkyl, optionally substituted alkyl, aryl or heterocyclyl; [159] R 2 is —NH 2 , —C (═O) NH 2 or —C (═O) OH; [160] R 3 is —H, alkyl, optionally substituted aryl or heterocyclyl; [161] R 5 is —C (═O) OH, tetrazolyl, —SO 3 H or —SONH 2 . [162] Typical VLA-4 inhibitors in this class of compounds are exemplified by the following formula 0.0.44 (European Patent No. 903 353; Hoechst Marion Russel Deutschland GmbH). [163] [164] Another group of inhibitory compounds that are structurally related to these compounds have been discovered by the Steeles and Wenner groups and described in European Patent No. 918 059 ("Substituted Imidazoline Derivatives with VLA-4 Antagonist Activity") in Wener et al. The group can be exemplified by the following formula 0.0.45: [165] [166] Where [167] R is methyl or phenyl; [168] R 1 is tert-butyl, propyl, isopropyl, benzyl, cyclohexyl or optionally substituted phenyl; [169] R 3 is adamantyl, —CH (CH 3 ) CH 2 C (═O) OH, optionally substituted —CH (phenyl) CH 2 C (═O) OH, or —CH (phenyl) CHC (= 0) OH; [170] R 4 is -H or iso-butyl. Examples of compounds that exemplify this class of VLA-4 inhibitors are compounds of the formula 0.0.46 (European Patent No. 918 059; Hoechst Marion Russel Deutschland GmbH). [171] [172] Another class of VLA-4 inhibitors is WO 99/10312, published by Chen et al., Assigned to F. Hoffmann-LaRoche AG ("Novel N-Aroylphenylalanine Derivatives As Integrin"). Antagonists ". Inhibitors of this class can be exemplified by the following formulas 0.0.47 and 0.0.48. The two subclasses of the compounds are based on different A rings, as shown below. [173] [174] [175] In addition, A and B rings may be replaced with various heterocycles, but ortho-substituted B rings are preferred. Representative examples of compounds in this class of inhibitors are compounds of the formula 0.0.49 (International Patent Publication No. WO99 / 10312; F. Hoffmann-La Roche Age). [176] [177] A closely related group of inhibitors found by the Chen group is described in International Patent Publication No. WO99 / 10313 to Chen et al. Assigned to F. Hoffmann-La Roche Age, which is illustrated by the following chemical formulas 0.0.50 and 0.0.51 Can be. The two subclasses of compounds are as described for the compounds of formulas 0.0.47 and 0.0.48. Typical compounds representative of this class of VLA-4 inhibitors are compounds of the formula 0.0.52 (International Patent Publication No. WO99 / 10313; F. Hoffmann-La Roche Age). [178] [179] [180] [181] A further class of inhibitors of VLA-4 dependent cell adhesion are, for example, Durette and Hagman's International Patent Publication No. WO98, assigned to Merck & Co., Inc. / 53814 (" Heterocyclic Amide Compounds As Cell Adhesion Inhibitors "), as found by Hagmann and its co-researchers. Compounds of this class can be exemplified by the following formula 0.0.53. [182] [183] X is -C (= 0) OH or an acid isoster; [184] Y is -C (= 0) or -S (= 0) 2 ; [185] R 1 to R 8 are selected from a variety of known substituents; [186] A, B and Z are chosen to provide heterocycles of different types and ring sizes. Examples of representative inhibitory compounds of this class are compounds of the formula 0.0.54 (International Publication No. WO98 / 53814; Merck & Co., Inc.). [187] [188] Another class of structurally related inhibitory compounds discovered by the Hagman group are described in WO 98/53817, entitled "Biarylalkanoic Acids As Cell Adhesion Inhibitors," by Dourette et al., Assigned to Merck & Company. ), Which can be illustrated by the following formulas 0.0.55 and 0.0.56. [189] [190] [191] Where [192] X, Y and R 1 to R 7 have substantially the same meanings as defined in formula 0.0.53; [193] Provided that R 2 and R 3 together with the atoms to which they are attached form a 4 to 7 membered ring containing 0 to 2 additional heteroatoms selected from O, S and N; [194] R b is optionally substituted alkyl, alkenyl, alkynyl, arylalkyl or heteroarylalkyl. Representative examples of compounds within this class of VLA-4 inhibitors are compounds of the formula 0.0.57 (International Publication No. WO98 / 53817; Merck & Company Incorporated). [195] [196] A further class of inhibitory compounds found by the Hagman group and structurally closely related to those described immediately above are described in International Patent Publication No. WO98 / 53818 (Durret et al., Assigned to Merck & Co., Ltd.). "Sulfonamides As Cell Adhesion Inhibitors". Such compounds can be exemplified by the following formulas 0.0.57a and 0.0.58. [197] [198] [199] Where [200] R b and R 1 to R 7 have the same meaning as defined in the formulas 0.0.55 and 0.0.56. Representative inhibitory compounds in this class are compounds of the formula 0.0.59 (WO 98/53818; Merck and Company Incorporated). [201] [202] A further class of VLA-4 inhibitory compounds structurally related to those described above was discovered by the Hagman Group and described in Delaszlo International Publication No. WO99 / 20272 ("Azapeptide Acids As Cell Adhesion Inhibitors"). Is initiated. Inhibitors of this class can be exemplified by the following formula 0.0.60. [203] [204] Where [205] m and n are 0 to 2; [206] X, Y and R 1 to R 6 have the same meaning as defined in the formulas 0.0.55 and 0.0.56. Representative inhibitory compounds within this class are compounds of the formulas 0.0.61 and 0.0.62 (International Patent Publication No. WO99 / 20272; Merck & Company Incorporated). [207] [208] [209] Another class of VLA-4 dependent cell adhesion inhibitors discovered by the Hagman group is Delaszlo and Hagman's International Patent Publication No. WO99 / 25685 ("4-Substituted", assigned to Merck & Company Inc.). 4-Piperidine Carboxamide Derivatives Useful in the Treatment of Asthma, Inflammation and Multiple Sclerosis ". Compounds of this class can be illustrated by the following formula 0.0.63. [210] [211] Where [212] X is a bonded or substituted carbon atom; [213] Z is -C (= 0) OH or an acid isoster; [214] L is -C (= 0)-, -S (= 0)-; [215] R 1 to R 5 have substantially the same meanings as defined in the formulas 0.0.55 to 0.0.56. Typical VLA-4 inhibitory compounds of this class are compounds of the formula 0.0.64 (WO 99/25685; Merck & Company Incorporated). [216] [217] Another class of VLA-4 that is structurally closely related to this compound is described in International Patent Publication No. WO 99/26615 to Chang et al. (Cyclic Amino Acids As Cell Adhesion), assigned to Merck & Co. Inhibitors ". This class of inhibitory compounds is illustrated by the following chemical formula 0.0.65. [218] [219] R represents ring size, [220] X, Y and R 1 to R 7 have the same meaning as defined in the formulas 0.0.55 and 0.0.56. Representative examples of inhibitory compounds in this class are compounds of the formula 0.0.66 (International Publication No. WO99 / 26615; Merck & Company Incorporated). [221] [222] Only a class of VLA-4 dependent cell adhesion inhibitors have been found which differ from the compounds disclosed in WO98 / 53814 only for terminal amino acids which are β-amino acids. Thus, reference may be made to Chemical Formula 0.0.53. Such β-amino acids are disclosed in International Patent Publication No. WO99 / 26921 ("Substituted β-Alanine Derivatives As Cell Adhesion Inhibitors"), issued by Durret et al., Assigned to Merco and Company. Typical inhibitors of this type are exemplified by the formulas 0.0.67 and 0.0.68. [223] [224] [225] A further class of VLA-4 dependent cell adhesion inhibitors structurally associated with these compounds has been discovered by Hagman Group and assigned to International Patent Publication No. WO99 / 26922 by Chang et al., Assigned to Merck & Co. "Substituted Pyrrole Derivatives As Cell Adhesion Inhibitors". Inhibitors of this class are exemplified by the following formula 0.0.69. [226] [227] Where [228] Y and R 1 to R 7 have the same meaning as defined in the formula 0.0.55 and 0.0.56, [229] X and Z have the same meaning as defined in Formula 0.0.63, [230] When -X-Z- in formula 0.0.63 is replaced with -Z-X- in formula 0.0.69, the meaning is reversed. Examples of inhibitory compounds in this class are exemplified by the following chemical formula 0.0.70 (WO 99/26922; Merck & Company Incorporated). [231] [232] Another class of VLA-4 inhibitory compounds found by the Hagman group and closely related to such compounds are Delaszlo and Hagman's International Patent Publication No. WO99 / 26923, assigned to Merck & Co. Para-Aminomethylaryl Carboxamide Derivatives ", which can be represented by the following formula 0.0.71. [233] [234] Where [235] L, X, Z and R 1 to R 6 have substantially the same meanings as defined in the formulas 0.0.55 and 0.0.56. Ar is a 1,4-substituted aryl or heteroaryl moiety. Typical compounds within the scope of this class of VLA-4 inhibitors are exemplified by the following formula 0.0.72 (International Publication No. WO99 / 26923; Merck & Company Incorporated). [236] [237] Another group is a novel class of VLA-described in International Patent Publication No. WO99 / 37605 ("VLA-4 Antagonists") of Watanasin and Von Matt, assigned to Novartis. 4 antagonists were found. This novel class of inhibitory compounds can be represented by the formula 0.0.73 [238] [239] Where [240] Y is -C (= 0)-, -S (= 0) 2 -or -P (= 0) 2- ; [241] Z is-(CH 2 ) n- , -CHR- or NR-; [242] W is -CH or -N-; [243] X is -C (= 0) OH or an acid isoster; [244] R 1 to R 4 are various common substituents. Representative examples of VLA-4 inhibitors from this class are illustrated by the following formula 0.0.74 (WO 99/37605; Novartis). [245] [246] Another group is Astles International Patent Publication No. WO99 / 23063 ("Substituted Anilides and Their Use in the Treatment of Various Disease States including inflammation," assigned to Rhone-Poulenc Rorer Ltd.). An additional class of compounds that inhibits VLA-4 dependent cell adhesion described in arthritis, and atherosclerosis "has been discovered. This class of VLA-4 inhibitors can be represented by the formula 0.0.75 [247] [248] Where [249] X 1 , X 2 and X 3 are -N- or -CR-; [250] Ar 1 is aryl or heteroaryl; [251] L 2 is an optionally substituted alkylene bridge; [252] Y is carboxy, acid bioisoster or -C (= 0) NRR; [253] R 1 is —H, halo, —OH, lower alkyl or lower alkoxy. Representative examples of inhibitory compounds of this class are exemplified by the following general formula 0.0.76 (WO 99/23063; Long-Pullen Roller Limited). [254] [255] Another class of VLA-4 inhibitors that are structurally closely related to the compounds described immediately above are those of Atles International Patent Publication No. WO99 / 33789 ("Biaryl β-Alanine Derivatives Useful", assigned to Long-Pullen Roller Limited). As VLA-4 Antagonists ". Compounds of this class may be represented by the formula 0.0.77. [256] [257] X 1 , X 2 and Y have the same meaning as defined in formula 0.0.75. R 4 is aryl or heteroaryl or optionally substituted alkyl, alkenyl or alkynyl. Representative examples of inhibitory compounds in this class are exemplified by the following formula 0.0.78 (WO 99/33789; Long-Fullen Roller Limited). [258] [259] In addition, another group is also disclosed in WO96 / 40871 ("Cyclic Peptide Inhibitors of β 1 and β 2 ", such as Lobi, assigned to Tanabe Seiyaku Co., Ltd.). A novel class of VLA-4 dependent cell adhesion inhibitors described in Integrin-Mediated Adhesion "have been discovered. Inhibitors are cyclic peptides containing free acid (WO96 / 40871; Tanabe Seiyaku Co., Ltd.). [260] Another class of VLA-4 inhibitors found by the same group is International Patent Publication No. WO98 / 58902, such as Ryou Tanabe Seiyaku Co., Ltd. and Rovi, assigned to Pharmacia & Upjohn Company. Inhibitors of α 1 β 4 Mediated Cell Adhesion ”. Members of this additional class of VLA-4 inhibitors can be represented by the formula 0.0.79 [261] [262] Where [263] R 1 is an acid or an amide; [264] X is phenyl; [265] Z is an amide or methylene ether. Representative examples of inhibitory compounds from this class are compounds of the formula 0.0.80 (WO 98/58902; Tanabe Seiyaku Co., Ltd.). [266] [267] Another class of VLA-4 inhibitors found by the same group is described in International Patent Publication No. WO99 / 36393 ("Inhibitors of α4 Mediated Cell Adhesion") by Sircar et al., Assigned to Tanabe Seiyaku Co., Ltd. do. The members of this class of VLA-4 inhibitors can be characterized by the formula 0.0.81. [268] [269] Where [270] R 1 to R 6 except R 4 are selected from various general substituents; [271] R 4 is an acid, an acid isoster or an amide; [272] A is aryl or heteroaryl; [273] Q is a bond, -C (= 0)-or substituted alkylene; [274] n is 0 to 2; [275] W is -O-, -S-, -CH = CH- or N = CH-. Representative members of this class of VLA-4 inhibitors are exemplified by the general formula 0.0.82 (WO99 / 36393; Tanabe Seiyaku Co., Ltd.). [276] [277] Another group is also disclosed in International Patent Publication No. WO96 / 00581 (Kogan et al., Entitled "Process to Inhibit Binding of the Integrin alpha 4 beta 1 to VCAM1 or Fibronectin", assigned to Texas Biotechnology Corporation). A new class of VLA-4 dependent cell adhesion inhibitors is described. This class of VLA-4 antagonists also includes cyclic peptides of 5 to 13 residues modeled after a portion of the CS1 peptide, containing free acid (International Publication No. WO96 / 00581; Texas Biotechnology Corporation). . [278] Another group also found a new class of VLA-4 antagonists described in Duta's International Patent Publication No. WO96 / 20216 ("Fibronectin Adhesion Inhibitors"), assigned to Zeneca Limited. VLA-4 antagonists of this class include cyclic peptides containing free acid (WO 96/20216; Geneca Limited). [279] A related class of VLA-4 antagonists found by the same group is described in Duta's International Patent Publication No. WO97 / 02289 ("Cyclic Tetrapeptide Dimers Useful As Fibronectin Inhibitors") assigned to Genca Limited. This class of VLA-4 antagonists includes cyclic dimeric peptides in which peptide 1 and peptide 2 independently representing tetrapeptides are juxtaposed in parallel or anti-parallel orientation by two crosslinking residues L1 and L2 (International Patent Publication No. WO97 / 02289; Geneca Limited). [280] Another related class of VLA-4 antagonists found by the same group is described in Duta's International Patent Publication No. WO97 / 49731 ("Cyclic Octapeptide Derivatives That Are Integrin Antagonists") assigned to Genca Limited. This class of VLA-4 antagonists includes a variety of cyclic octapeptides containing free acids (WO97 / 49731; Geneca Limited). [281] The same group also found a non-peptidal class of VLA-4 antagonists described in International Patent Publication No. WO99 / 24398 ("Chemical Compounds") of Brittany and Johnstone, assigned to Genca Limited. Members of this class can be represented by the formula 0.0.83. [282] [283] Where [284] Y is -O-, -S or -S (= 0) 2- ; [285] R 1 is urea; [286] R 11 is acid or acid isoster; [287] m is 0 or 1, when m is 0, n is 1 to 4, and when m is 1, n is 0. Representative members of this class of VLA-4 antagonists are exemplified by the following formula 0.0.84 (International Publication No. WO99 / 24398; Geneca Limited). [288] [289] None of the references discussed above discloses or suggests a compound of the present invention. [290] Despite these advances in the art in VLA-4 mediated cell adhesion, those skilled in the art are prone to poor absorption and solubility and are metabolized in vivo (systemically and topically when administered directly through the lungs). All) It will soon be appreciated that it reduces the chance of significant impact on the course of inflammatory, respiratory or autoimmune diseases. [291] This allows the non-peptidal, ie class of VLA-4 antagonists that can be considered as small molecules, to avoid the tendency of the peptidal agents discussed above. However, small molecule VLA-4 antagonists known in the art, as described in detail above, may be suitable therapeutic pharmacokinetics and absorption, where such compounds may be suitable therapeutic agents for use in treating the diseases and conditions discussed herein. It has been established that with a profile there is a low level of acceptable side effects while not having a sufficiently high level of desired potential. Thus, there is still a need in the art for non-peptide-based or semipeptidyl therapeutics that can effectively treat or prevent such pathological conditions. [292] Summary of the Invention [293] The present invention relates to a composition for inhibiting VLA-4 dependent cell adhesion in a mammal. The present invention relates to compounds of formula 1.0.0 and pharmaceutically acceptable salts and other prodrug derivatives thereof. [294] [295] Where [296] A is (C 1 -C 6 ) alkyl, cycloalkyl, aryl, heteroaryl or heterocyclyl [these radicals are as defined herein and the radical alkyl, cycloalkyl, aryl, heteroaryl or heterocyclyl Optionally substituted with 0 to 3 substituents identical to R 9 , defined below; or A 1 -NHC (= 0) NH-A 2- , A 1 -NHC (= 0) OA 2- , A 1- OC (= O) NH-A 2- , A 1 -NHSO 2 NH-A 2- , A 1 -NHC (= O) -A 2- , A 1 -C (= O) NH-A 2- , A 1 -NHSO 2 -A 2- , A 1 -SO 2 NH-A 2- , A 1- (CH 2 ) r -A 2- , A 1 -CH (R 1 ) -OA 2- , A 1- ( CH 2 ) r OA 2- , A 1 -O (CH 2 ) r -A 2- , A 1- (CH 2 ) r NH-A 2- , A 1 -NH (CH 2 ) r -A 2- , And A 1- (CH 2 ) r S (= 0) q -A 2- , wherein A 1 and A 2 are each independently hydrogen, aryl, (C 1 -C 6 ) alkyl, (C 2 -C 6 ) Alkenyl, (C 2 -C 6 ) alkynyl, cycloalkyl, heteroaryl and heterocyclyl, wherein said aryl, alkyl, cycloalkyl, Heteroaryl or heterocyclyl group is a component selected from the group consisting of radicals of 0 to 3 substituents equal to R 9 defined below; [297] B is a component independently selected from the group consisting of residues of the partial formulas 1.1.0 to 1.1.23; [298] E is a single bond; -O-; -NR 10- , -CH = CH-, -C≡C-; -S (= 0) q- ; -CR 11 R 12 NR 10- ; Or -CR 11 R 12- ; [299] X is -O-; -C (= 0)-; -S (= 0) q- ; Or -NR 10- ; [300] X 1 , X 2 and X 3 are each independently CH; CR 9 ; And N; [301] Y is a single bond; -C (= 0)-; -C (= S)-; Or -S (= 0) 2- ; [302] k is an integer independently selected from 0, 1 and 2; [303] m is an integer independently selected from 0 and 1; [304] n is an integer independently selected from 0, 1 and 2; [305] p is independently an integer of 0 or 1 and should be selected to 1 when B is selected as a residue of partial formula 1.1.0 to 1.1.11; [306] q is an integer independently selected from 0, 1 and 2; [307] r is an integer independently selected from 0, 1 and 2; [308] R 1 is (C 1 -C 3 ) alkyl substituted with 0 or 1 F; CF 3 ; OCF 3 ; Or cyano; [309] R 2 and R 3 are each independently hydrogen; A (C 1 -C 6) alkyl, optionally substituted by R 13 and the same 0 to 3 substituents as defined below (C 2 -C 6) optionally substituted with R 13 to define with the same 0 to 3 substituents alkenyl, defined below substituted with the same 0 to 3 substituents, and R 13 is (C 3 -C 14) carbocyclic ring system, the following definitions and R 13 is substituted by 0 to 3 substituents the same The same heterocyclyl ring as defined herein, substituted with (C 1 -C 6 ) alkyl-OR 5 , substituted with 0 to 3 substituents identical to R 13 as defined below, 0 to 3 R 13 (C 1 -C 6 ) alkyl-SR 5 , (C 1 -C 6 ) alkyl-SO 2 R 5 , 0 to 3 R substituted by 0 to 3 substituents the same as R 13 defined below 13 is substituted the same 0 and R 13 is the same heteroaryl ring, and to define as defined herein Which it is substituted by three substituents, and are each independently selected from the group consisting of the same aryl ring as defined herein; [310] Provided that R 2 and R 3 are each the same as defined above; Together they form a ring as defined below; One of which together with R 4 forms a group as defined below in which case the other is hydrogen or methyl; [311] R 2 and R 3 together form a cycloalkyl or heterocyclyl ring substituted by 0 to 3 substituents same as R 13 , defined below; [312] R 2 or R 3 is the same heteroaryl or heterocyclyl as defined herein and substituted by R 4 , and 0 to 3 substituents identical to R 13 , defined below, together with the carbon and nitrogen atoms to which they are attached, respectively; To form a group; [313] R 4 is hydrogen; Or (C 1 -C 6 ) alkyl optionally substituted by the same substituent R 13 as defined below, or R 4 together with R 2 or R 3 form a carbocyclic or heterocyclic ring; [314] R 5 and R 6 are independently hydrogen; Or (C 1 -C 6 ) alkyl; (C 2 -C 6 ) alkenyl; (C 2 -C 6 ) alkynyl; CF 3 ; Aryl; Cycloalkyl; Heteroaryl; Or heterocyclyl, wherein the alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heteroaryl or heterocyclyl is substituted by 0 to 3 substituents equal to R 13 defined below; [315] R 7 is (C 1 -C 6 ) alkyl; (CH 2 ) k OR 5 ; (CH 2 ) k C (= 0) R 5 ; (CH 2 ) k C (= 0) NR 6 R 5 ; (CH 2 ) k NR 6 C (= 0) R 5 ; (CH 2 ) k NR 6 C (= 0) OR 5 ; (CH 2 ) k NR 6 SO 2 R 5 ; (CH 2 ) k NR 6 R 5 ; F; CF 3 ; OCF 3 ; Aryl substituted with 0 to 3 substituents identical to R 9 defined below; Heterocyclic substituted by 0 to 3 substituents equal to R 9 defined below; Heteroaryl substituted by 0 to 3 substituents the same as R 9 defined below; Or cycloalkyl substituted by 0 to 3 substituents equal to R 9 defined below; R 7 may form a cycloalkyl or heterocyclic ring with R 8 ; R 7 may form a cycloalkyl or heterocyclyl ring with R 11 ; [316] R 8 is hydrogen; F; CN; (C 1 -C 6 ) alkyl or (C 1 -C 6 ) alkoxy; [317] R 9 is hydrogen; (C 1 -C 6 ) alkyl; (C 1 -C 6 ) alkoxy; (C 3 -C 6 ) cycloalkyl; (C 3 -C 6 ) cycloalkoxy; Cyano; (CH 2 ) k OH; C (= 0) R 5 ; (CH 2 ) k C (O) NR 5 R 6 ; (CH 2 ) k NR 6 SO 2 R 5 ; CF 3 ; OCF 3 ; SO 2 NR 5 R 6 ; Or (CH 2 ) m C (= 0) OR 5 ; When R 9 is bonded to a saturated carbon atom R 9 may be = O or = S; R 9 may be ═O when R 9 is bonded to a sulfur atom; [318] R 10 is hydrogen; C (= 0) R 5 ; C (= 0) OR 5 ; (C 1 -C 6 ) alkyl; Aryl; Heterocyclyl; Heteroaryl; Cycloalkyl; Or SO 2 R 5 ; [319] R 11 and R 12 are independently hydrogen; (C 1 -C 6 ) alkyl; Hydroxy; Cyano; (C 1 -C 6 ) alkoxy; NR 6 C (= 0) R 5 ; NR 6 SO 2 R 5 ; NR 6 R 5 ; CF 3 ; F; Aryl; Heterocyclyl; Heteroaryl; Cycloalkyl; Or cycloalkoxy; R 11 may form a cycloalkyl or heterocyclic ring with R 12 ; [320] R 13 is halogen; CF 3 ; (C 1 -C 6 ) alkyl; Aryl; Heteroaryl; Heterocyclyl; Hydroxy; Cyano; (C 1 -C 6 ) alkoxy; (C 3 -C 6 ) cycloalkyl; (C 3 -C 6 ) cycloalkoxy; (C 2 -C 6 ) alkynyl; (C 2 -C 6 ) alkenyl; -NR 6 R 5 ; -C (= 0) NR 5 R 6 ; SO 2 R 5 ; C (= 0) R 5 ; NR 5 SO 2 R 6 ; NR 5 C (= 0) R 6 ; C (= 0) NR 5 SO 2 R 6 ; NR 5 C (= 0) OR 6 ; And SO 2 NR 6 R 5 . [321] [322] [323] [324] [325] [326] [327] [328] [329] [330] [331] [332] [333] [334] [335] [336] [337] [338] [339] [340] [341] [342] [343] [344] [345] Where [346] The indication of "*" indicates the point at which the moiety of each partial formula 1.1.0 to 1.1.23 binds to the residue "CR 2 R 3 " of formula 1.0.0, [347] The indication of "→" indicates the point at which the moiety of each partial formula 1.1.0 to 1.1.23 binds to the residue "E" of formula 1.0.0, [348] Residues of each partial formula 1.1.0 to 1.1.23 may be optionally substituted with R 9 except for the residues of partial formula 1.1.10, 1.1.17 and 1.1.23. [349] The invention also relates to one or more compounds of the invention and the compound (s) which are effective in preventing, inhibiting, preventing or reducing cell adhesion and subsequent or associated pathogenic processes after the amount of compound is mediated by VLA-4. It relates to a pharmaceutical composition comprising a pharmaceutically acceptable carrier. The present invention also relates to pharmaceutical compositions which contain one or more therapeutic agents selected from the group consisting of anti-inflammatory corticosteroids, nonsteroidal anti-inflammatory agents, bronchodilators, asthma therapeutic agents and immunosuppressive agents, in addition to containing the compounds of the present invention. [350] Moreover, the present invention is directed to the inhibition of cell adhesion and subsequent or associated pathogenic processes mediated by VLA-4, comprising administering a therapeutically effective amount of a pharmaceutical composition of the invention to a mammal in need of such treatment. A method of treating or preventing inflammatory, autoimmune or respiratory diseases. The pharmaceutical compositions of the present invention include, but are not limited to, asthma, multiple sclerosis, rheumatoid arthritis, osteoarthritis, inflammatory bowel disease, psoriasis, host rejection after organ transplantation, atherosclerosis, and other diseases mediated or associated with VLA-1. It can be used to treat many inflammatory, autoimmune and respiratory diseases, including but not limited to. [1] The present invention is a very recent antigen to proteins such as Vascular Cell Adhesion Molecule-1 (VCAM-1) which is structurally non-peptidyl and is a HepII / IIICS domain (CS-1 region) of fibronectin and osteopontin. A compound having activity as a potential inhibitor of binding of -4 (VLA-4; α 4 β 1 ; CD49d / CD29). On their own, they are useful for the inhibition of cell adhesion and subsequent or associated pathogenic processes mediated by VLA-4. The compounds and pharmaceutical compositions of the present invention can be used for the treatment of many inflammatory, autoimmune and respiratory diseases, especially asthma. [351] The present invention relates to compounds that inhibit cell adhesion and subsequent pathogenesis mediated by VLA-4. Therefore, such compounds useful for the treatment of a number of inflammatory diseases, autoimmune diseases and respiratory diseases can be represented by the formula 1.0.0. [352] Formula 1.0.0 [353] [354] In the compound of Formula 1.0.0, the terminal group represented by A is alkyl, cycloalkyl, aryl, heteroaryl or heterocyclyl substituted with 0 to 3 R 9 or A 1 -NHC (═O) NH— A 2- , A 1 -NHC (= O) OA 2- , A 1 -OC (= O) NH-A 2- , A 1 -NHSO 2 NH-A 2- , A 1 -NHC (= O)- A 2- , A 1 -C (= O) NH-A 2- , A 1 -NHSO 2 -A 2- , A 1 -SO 2 NH-A 2- , A 1- (CH 2 ) r OA 2- , A 1 -O (CH 2 ) r -A 2 , and A 1- (CH 2 ) r -A 2- , wherein A 1 and A 2 are each independently hydrogen, aryl, alkyl, alkenyl, alkynyl From the group consisting of cycloalkyl, heteroaryl and heterocyclyl, wherein the aryl, alkyl, alkenyl, cycloalkyl, heteroaryl or heterocyclyl group is substituted with 0 to 3 R 9 ) Selected ingredient. [355] The term "A" and "alkyl" used alone or in combination throughout this specification generally refers to straight or branched chain alkyl radicals of 1 to 6 carbon atoms, often 1 to 4 carbon atoms. Examples of such radicals include, but are not limited to, methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, pentyl, iso-amyl and hexyl. [356] The term "A" and "cycloalkyl" used alone and in combination throughout this specification refers to a cyclic alkyl radical having 3 to 6 carbon atoms. Examples of such cycloalkyl radicals include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and the like. [357] The term "A" and "aryl" as used throughout this specification refers to carbocyclic aromatic groups that are components selected from the group consisting essentially of phenyl, naphthyl, indenyl, indanyl, and fluorenyl. However, when "A" is "aryl", the case of phenyl is preferable. [358] The term "A" and "heteroaryl" as used throughout the specification refers to furyl, thienyl, pyrrolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, imidazolyl, imidazolinyl, pyrazolyl, Pyrazolinyl, oxadiazolyl, thiadiazolyl, triazolyl, pyridyl, pyrazinyl, pyridazinyl, pyrimidinyl, triazinyl, pyranyl, parathiazinyl, indolyl, isoindoleyl, 3H-indolyl , Indolinyl, benzo [b] furanyl, 2,3-dihydrobenzofuranyl, benzo [b] thiophenyl, 1H-indazolyl, benzimidazolyl, benzoxazolyl, benzthiazolyl, furinyl, qui Nolinyl, isoquinolinyl, 4H-quinolininyl, cynolinyl, phthalazinyl, quinazolinyl, quinoxalinyl, 1,8-naphthyridinyl, putridinyl, carbazolyl, acridinyl, phena Heterocyde, a component selected from the group consisting essentially of genyl, phenothiazinyl, phenoxazinyl, and pyrazolol [1,5-c] triazinyl Rick is intended to refer to an aromatic group. [359] However, when "A" is "heteroaryl", furyl, thienyl, pyrrolyl, oxazolyl, isoxazolyl, thiazolyl, imidazolyl, pyridyl, pyrimidinyl, indolyl, benzo [b] Preference is given to furanyl, benzimidazolyl or quinolinyl. More preferably "A" is pyridyl. [360] The terms "heterocyclic" and "heterocyclyl" as used throughout "A" and the specification, refer to non-aromatic 3- to 10-membered wherein one or more carbon atoms of the ring is substituted by a heteroatom selected from N, O or S. Refers to a carbocyclic ring of. Preferably at least two heteroatoms are present, in the case of nitrogen there may be 4 N heteroatoms. Heterocyclyl groups may include one or two conjugated rings, and may further include aryl-conjugated rings. Preferably, "heterocyclyl" means essentially oxiranyl, pyrrolidinyl, pyrazolidinyl, imidazolidinyl, tetrazolidinyl, piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl and benzo Refers to a component selected from the group consisting essentially of dioxolane, in particular 1,3-benzodioxol-5-yl. [361] However, when "A" is "heterocyclyl", it is preferred to be pyrrolidinyl, piperidinyl, piperazinyl or morpholinyl. [362] When “A” is defined as a residue selected from an alkyl, cycloalkyl, aryl, heteroaryl or heterocyclyl group as defined above, said residue may be substituted with 0 to 3 R 9 . "0" means no substituent and substitution is optional. When substituted, it is preferred that there are two substituents, more preferably only one substituent. [363] When a substituent of R 9 is used, halogen, (C 1 -C 6 ) alkyl, (C 1 -C 6 ) alkoxy, (C 3 -C 6 ) cycloalkyl, (C 3 -C 6 ) cycloalkoxy, cya Furnace, hydroxy, C (= O) R 5 , C (O) NR 5 R 6 , NR 5 R 6 , NR 5 SO 2 R 6 , CF 3 , OCF 3 , SO 2 NR 5 R 6 , C (= O) oR 5 (wherein when R 9 is bonded to a saturated carbon atom, R 9 is = O or = may be S, if R 9 is bonded to a sulfur atom, R 9 may be a = O, R 5 and R 6 are as further defined herein.) And independently from the group consisting essentially of However, preferably one substituent is F, Cl, OH, methyl, methoxy, cyclohexyl, acetyl, cyclopropyloxy or F 3 C-. [364] Substituent "R 9 " on group "A" and the term "alkoxy" used alone or in combination herein refers to an alkyl ether radical, wherein the term "alkyl" is as described above. . Examples of suitable alkyl ether radicals include, but are not limited to, methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, iso-butoxy, sec-butoxy and tert-butoxy. no. [365] Substituent "R 9 " on group "A" and the term "cycloalkoxy" used alone or in combination refer to a cycloalkyl ether radical, wherein the term "cycloalkyl" refers to Same as one. Examples of suitable cycloalkoxy radicals include, but are not limited to, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, and cyclohexyloxy. [366] Preferred meaning of "A" is A 1 -NHC (= O) NH-A 2- , A 1 -NHC (= O) OA 2- , A 1 -OC (= O) NH-A 2- , A 1- NHSO 2 NH-A 2- , A 1 -NHC (= O) -A 2- , A 1 -C (= O) NH-A 2- , A 1 -NHSO 2 -A 2- , A 1 -SO 2 NH-A 2- , A 1- (CH 2 ) r -A 2- , A 1 -CH (R 1 ) -OA 2- , A 1- (CH 2 ) r -OA 2- , A 1 -O ( CH 2 ) r -A 2- , A 1- (CH 2 ) r NH-A 2- , A 1 -NH (CH 2 ) r -A 2- , and A 1- (CH 2 ) r S (= 0 ) qA 2- (wherein A 1 and A 2 are each independently from the group consisting of hydrogen, aryl, (C 1 -C 6 ) alkyl, cycloalkyl, heteroaryl and heterocyclyl, said aryl, alkyl, cycloalkyl , Heteroaryl or heterocyclyl group is a divalent radical which is a component selected from the group consisting of radicals of 0 to 3 R 9 ). The alkyl, cycloalkyl, aryl, heteroaryl or heterocyclyl group, bonded to one or both of the ureido radicals, is selected according to the above definition as in the 0 to 3 substituents R 9 . It is preferable that an aryl group is covalently bonded to both of a ureido radical, and it is preferable that such an aryl group is phenyl. Most preferably, the phenyl group has a single substituent which is preferably F, Cl, methyl, methoxy or F 3 C-. Examples of the preferred meaning of "A" are shown in part by moieties of the partial formulas 4.0.0 to 4.0.11 below. [367] [368] [369] [370] [371] [372] [373] [374] [375] [376] [377] [378] [379] The component of the compound of formula 1.0.0 adjacent to the "A" component is a single bond, methylene or ethylene bridge element when n, 0, 1 or 2, respectively. Preference is given to n being 1 and a methylene bridge. Thus, among the above-mentioned preferred for the meaning of component "A", a methylene bridge is added and the following most preferred terminal portion comprising component "A" can be represented by the moieties of the following partial formulas 4.1.0 to 4.1.23: [380] [381] [382] [383] [384] [385] [386] [387] [388] [389] [390] [391] [392] [393] [394] [395] [396] [397] [398] [399] [400] [401] [402] [403] [404] Further, the moieties of the partial formulas which are preferably bound to the N, N'-diphenylureido groups in the para position with respect to the point of attachment of the divalent ureido group to the phenyl group containing the preferred methylene bridge will be discussed further. [405] The “Y” component of Formula 1.0.0 may be —C (═O), —C (═S), or —S (═O) 2 —. However, it is most preferred that, in total, "Y" is a carbonyl residue, ie "Y" is a -C (= 0) residue. [406] The next component of the compound of formula 1.0.0 is -NR 4 CR 2 R 3- . In this component, R 2 and R 3 are independently hydrogen, 0 to 3 R 13 a (C 1 -C 6) alkyl, substituted with 0 to 3 R 13 (C 2 -C 6 substituted by each ) alkenyl substituted with 0 to 3 R 13 (C 3 -C 14) carbocyclic ring system, substituted with 0 to 3 R 13 a heterocyclic ring, and 0, as defined herein, more to the replacement of three R 13 (C 1 -C 6) alkyl, -OR 5, 0 to 3 of one R 13 substituted (C 1 -C 6) alkyl, -SR 5, 0 to 3 R 13 with substituted (C 1 -C 6) alkyl, -SO 2 R 5, being substituted with 0 to 3 R 13 is substituted with a heteroaryl ring, and 0 to 3 R 13 as defined herein, as defined herein Each independently selected from the group consisting of aryl rings as shown. R 2 and R 3 are bonded to each other according to the optional definition of R 2 and R 3 , in which case they form a cycloalkyl or heterocyclyl ring substituted with 0 to 3 R 13 . For example, when R 2 and R 3 are bonded to each other to form a spirocyclic cyclopropyl, cyclobutyl, or cyclopentyl group, the resulting compound of the present invention is a residue of the following partial formulas 1.2.0 to 1.2.2 It will include. [407] [408] [409] [410] Other preferred sub-groups of the compounds of the present invention are those in which R 2 or R 3 combine with R 4 and the carbon and nitrogen atoms to which they are bonded to form a heteroaryl or heterocyclyl group as described above. The heteroaryl or heterocyclic group may again be substituted with 0 to 3 R 13 . According to the foregoing, when R 2 or R 3 binds to R 4 , the other must be hydrogen or methyl. Sub-groups can be represented by the moieties of the partial formula 1.3.0: [411] [412] Where [413] The indication of "*" indicates the point where the residue of Formula 1.3.0 binds to the residue "Y" of Formula 1.0.0, [414] The indication of "→" indicates the point where the moiety of the partial formula 1.3.0 binds to "B" of the formula 1.0.0 represented by the formula 1.1.0 to 1.1.22. Substituent “R 2/3 ” indicates that R 2 substituent or R 3 substituent is present. Since one or the other is already selected to combine with R 4 to form a heteroaryl or heterocyclyl group of the partial partial formula 1.3.0a below, both may not be present. [415] [416] It will be understood that if R 2 or R 3 is present, it may be hydrogen, alkyl or methyl. [417] Thus, the sub-group of “-NR 4 CR 2 R 3 B-”, which is a residue of partial formula 1.3.0, may include embodiments of the residues of partial formulas 1.3.1 to 1.3.20, including but not limited to no: [418] [419] [420] [421] [422] [423] [424] [425] [426] [427] [428] [429] [430] [431] [432] [433] [434] [435] [436] [437] [438] Where [439] The indication of "*" indicates the point where each partial residue of Formulas 1.3.1 to 1.3.20 binds to the "Y" residue of Formula 1.0.0, [440] The designation of "→" indicates the point where each partial residue of Formulas 1.3.1 to 1.3.20 binds to the "E" residue of Formula 1.0.0. [441] According to the optional substituent R 13 , which may be present in the R 2 and R 3 substituents of the B component, there is no “R 13 ” when “0” is selected. R 13 is absent or halogen, CF 3 , (C 1 -C 6 ) alkyl, aryl, heteroaryl, heterocyclyl, hydroxy, cyano, (C 1 -C 6 ) alkoxy, (C 3 -C 14 ) Carbocyclic ring system, (C 3 -C 6 ) cycloalkoxy, (C 2 -C 6 ) alkynyl, (C 2 -C 6 ) alkenyl, -NR 6 R 5 , -C (= 0) NR 5 R 6 , SO 2 R 5 , C (= O) R 5 , NR 5 SO 2 R 6 , NR 5 C (= O) R 6 , C (= O) NR 5 SO 2 R 6 , NR 5 C ( Preferred is a single substituent selected from ═O) OR 6 and SO 2 NR 5 . In the optional substituent R 13 and the remainder of this specification, the term "alkynyl" used alone or in combination refers to a straight or branched chain alkynyl radical having 2 to 6 carbon atoms, preferably 2 to 4 carbon atoms. . Examples of such radicals include, but are not limited to, ethynyl (acetylenyl), propynyl, propargyl, butynyl, hexynyl, decinyl, and the like. [442] In the definition of R 13 , the term “alkenyl” used alone or in combination refers to a straight or branched chain alkenyl radical having 2 to 6 carbon atoms, preferably 2 to 4 carbon atoms. Examples of such radicals include ethenyl, E- and Z-propenyl, iso-propenyl, E- and Z-butenyl, E- and Z-iso-butenyl, and E- and Z-pentenyl However, this is not limitative. [443] The term "(C 3 -C 14 ) carbocyclic ring system" as used throughout the specification as well as for R 2 and R 3 , alone or in combination, comprises one, two or three conjugates of 3 to 14 carbon atoms. It refers to a cycloalkyl and cycloalkenyl group composed of rings. The term "cycloalkyl" also means a cyclic alkyl radical having 3 to 8 carbon atoms, preferably 3 to 6 carbon atoms. Examples of such cycloalkyl radicals include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and the like. On the other hand, the term "cycloalkenyl" includes cyclic carbocycles containing 4 to 8 carbon atoms, preferably 5 or 6 and one or two double bonds. Examples of such cycloalkenyl radicals include, but are not limited to, cyclopentenyl, cyclohexenyl, and cyclopentadienyl. [444] If two or three conjugated rings are present, one of the rings may be a cycloalkyl ring system and the other one or two rings may be a cycloalkenyl ring system. [445] One of R 2 and R 3 is hydrogen and the other is hydrogen, methyl, ethyl, propyl, butyl and iso-butyl; Hydroxymethyl, methoxymethyl; Allyl, propenyl, E- and Z-iso-butenyl and E- and Z-pentenyl; Cyclopropylmethyl, cyclopentylmethyl and cyclohexylmethyl; Cyclohexenylmethyl, benzyl, benzyloxymethyl and phenoxymethyl; 2- (methylthio) ethyl; 3- (hydroxypropylthio) methyl; 2- (methylsulfonyl) ethyl; 4- (acetylamino) butyl; 4- (methylsulfonylamido) butyl; And 4-ethoxycarbonylamido) butyl. [446] The next component, the “B” group of the compound of formula 1.0.0, is one of the more important parts of the molecule and is important in providing the unexpected good biological properties possessed by the compounds of the invention. Group “B” is selected from the components consisting of the moieties of the following partial formulas 1.1.0 to 1.1.22: [447] Chemical Formula 1.1.0 [448] [449] Formula 1.1.1 [450] [451] Formula 1.1.2 [452] [453] Formula 1.1.3 [454] [455] Chemical Formula 1.1.4 [456] [457] Formula 1.1.5 [458] [459] Formula 1.1.6 [460] [461] Chemical Formula 1.1.7 [462] [463] Chemical Formula 1.1.8 [464] [465] Formula 1.1.9 [466] [467] Formula 1.1.10 [468] [469] Formula 1.1.11 [470] [471] Formula 1.1.12 [472] [473] Formula 1.1.13 [474] [475] Formula 1.1.14 [476] [477] Formula 1.1.15 [478] [479] Formula 1.1.16 [480] [481] Formula 1.1.17 [482] [483] Formula 1.1.18 [484] [485] Formula 1.1.19 [486] [487] Formula 1.1.20 [488] [489] Formula 1.1.21 [490] [491] Formula 1.1.22 [492] [493] Where [494] The indication of "*" represents the point where each residue of Formula 1.1.0 to 1.1.22 binds to the residue "CR 2 R 3 " of Formula 1.0.0, [495] The designation of "→" indicates the point where each residue of Formula 1.1.0 to 1.1.22 binds to residue "E" of Formula 1.0.0. [496] All of the above-mentioned partial moieties of the formulas 1.1.0 to 1.1.22 are exemplified as segments in the same manner as described above, wherein both binding points at the ends of the specific segments are indicated by "*" and "→" marks. [497] In the moieties of the above partial formula which define the "B" component of the compound of formula 1.0.0, the residue "X" is oxygen, sulfur (q = 0) and sulfur to which two oxygen atoms are bonded (q = 2), ie , Sulfonyl; Or NH (if R 10 is hydrogen) or substituted nitrogen (if R 10 is (C 1 -C 6 ) alkyl, (C 3 -C 6 ) cycloalkyl, heterocyclyl, heteroaryl or aryl) have. However, it is preferred that "X" is only oxygen, sulfur or NH. [498] To component B of the compound of formula 1.0.0 is bound the remaining structural element represented by the moiety of the formula (part 1.4.0): [499] [500] It will first be noted that the moieties of the partial formula 1.4.0 may directly bond to component B of the entire compound of formula 1.0.0. E is a single bond, oxygen, —NR 10 —, —CH═CH—, or —CR 11 R 12 . [501] When substituent R 10 is used, it is independent from the group consisting essentially of hydrogen, C (= 0) R 5 , (C 1 -C 6 ) alkyl, aryl, heterocyclyl, heteroaryl, cycloalkyl or SO 2 R 6 Will be selected. [502] When substituents R 11 and R 12 are used, they are hydrogen, (C 1 -C 6 ) alkyl, hydroxy, (C 1 -C 6 ) alkoxy, NR 6 COR 5 , NR 6 SO 2 R 5 , NR 6 R 5 , CF 3 , F, aryl, heterocyclyl, heteroaryl, cycloalkyl and cycloalkoxy will be independently selected from the group consisting of. R 11 may be combined with R 12 to form a cycloalkyl or heterocyclic ring. R 5 and R 6 are independently selected from hydrogen, (C 1 -C 6 ) alkyl, CF 3 , aryl, cycloalkyl, heteroaryl or heterocyclyl. [503] The (C 1 -C 6 ) alkyl, (C 1 -C 6 ) alkoxy, aryl, heterocyclyl, heteroaryl, cycloalkyl and cycloalkoxy groups have already been defined above. Within the definition of this group, R 11 and R 12 are groups consisting of methyl, ethyl, propyl, butyl, iso-butyl, methoxy, cyclopropoxy, cyclopropyl, phenyl, morpholinyl, piperidinyl and pyridyl It is preferably selected independently from. [504] In some of the compounds of the present invention represented by the moieties of the aforementioned partial formula 1.4.0, residue E is a selective methylene of general formula (-CH 2- ) m where m is an integer independently selected from 0 and 1 It comes out behind the bridge. [505] The next component of formula (1.0.0) is represented by the general formula-(CR 7 R 8 ) p- (wherein "p" is selected from integers 0 and 1, provided that B is a residue of partial formulas 1.1.0 to 1.1.11 If selected, "p" must be 1). [506] Substituent "R 7 " is (C 1 -C 6 ) alkyl; Hydroxy; (C 1 -C 6 ) alkoxy; NHC (= 0) R 5 ; NHSO 2 R 5 ; NR 6 R 5 ; F; CF 3 ; OCF 3 ; Aryl; Heterocyclyl; Heteroaryl; Or from a group consisting of cycloalkyl, or R 7 may be linked to R 6 to form a cycloalkyl or heterocyclyl ring. Substituent R 8 is hydrogen; F; (C 1 -C 6 ) alkyl or (C 1 -C 6 ) alkoxy. [507] The final component of Formula 1.0.0 is the general formula -C (= 0) OR, where R is hydrogen. [508] Components represented by the residues of partial formula 1.4.0 are embodiments represented by, but not limited to, residues of the following partial formulas 1.4.1 to 1.4.20: [509] [510] [511] [512] [513] [514] [515] [516] [517] [518] [519] [520] [521] [522] [523] [524] [525] [526] [527] [528] [529] Pharmaceutically acceptable derivatives of the compound of formula 1.0.0 are also within the scope of the present invention. The expression "pharmaceutically acceptable derivative" as used herein refers to any pharmaceutically acceptable salt of a compound of Formula 1.0.0. In addition, any other compound that can directly or indirectly provide a compound of Formula 1.0.0 in administration to a patient is within the scope of the present invention. Such compounds are known as prodrugs and many known methods are useful for preparing such prodrug forms of the compound of Formula 1.0.0. [530] The term "patient" as described above and used throughout this specification refers to mammals, including humans. When the term "cell" is used, it refers to mammalian cells, including human cells, unless otherwise noted. [531] Residues or metabolites of compounds of Formula 1.0.0 that retain biological activity to inhibit cell adhesion and subsequent or related pathogenesis mediated by VLA-4 are also within the scope of the present invention. Once synthesized, the inhibitory activity and VLA-4 specificity of the compound of formula 1.0.0 according to the present invention can be measured using in vitro and in vivo assays specified specifically below. [532] Preferred biological activity of the compound of formula 1.0.0 by attaching a suitable functional group which acts to improve the expressed biological properties of the compound, to improve the selectivity for the biological activity present or to add the biological activity present in the desired biological activity. Can be improved. Such modifications are known in the art and increase biological penetration into established biological systems such as blood, lymphatic and central nervous system, and increase oral bioavailability; Increased solubility to enable injection administration; Modifying metabolic processes; And modifying the rate of release of the compound of formula 1.0.0. [533] In the foregoing definitions and in the present specification, other chemical and biological terms used herein can be easily understood by those skilled in the art. The defined terms may be used alone or in combination. Preferred or more preferred chain lengths of the radicals specified herein apply to all such combinations. [534] According to certain preferred subterms and more preferred subterm definitions for the compounds of Formula 1.0.0, the preferred and more preferred species are listed as follows to further illustrate the invention: [535] Compounds having residues of partial formula 1.1.0 [536] 3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4,5-dihydro -Oxazol-5-yl] -2-methyl-propionic acid; [537] 2-acetylamino-3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4 , 5-dihydro-oxazol-5-yl] -propionic acid; [538] 2-methanesulfonylamino-3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4,5-dihydro-oxazol-5-yl] -propionic acid; [539] 2,2-difluoro-3- {2- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- 4,5-dihydro-oxazol-5-yl} -propionic acid; [540] 2,2-dimethyl-3- [2- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -4,5- Dihydro-oxazol-5-yl] -propionic acid; [541] 2-allyloxycarbonylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4 , 5-dihydro-oxazol-5-yl} -propionic acid; [542] 2- (butane-1-sulfonylamino) -3- (2-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -4,5-dihydro-oxazol-5-yl) -propionic acid; [543] 2-Methyl-3- [2- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -4,5-dihydro-oxazole- 5-yl] -propionic acid, [544] 2-formylamino-3- {2- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -4,5-dihydro-thiazol-5-yl} -propionic acid , [545] 2-methyl-3- (2- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -4,5-dihydro-oxazol-5-yl) Propionic acid, [546] 2-benzenesulfonylamino-3- (2- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -4,5-dihydro-oxazole-5- Yl) -propionic acid, [547] 2-benzenesulfonylamino-3- [2- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- 4,5-dihydro-oxazol-5-yl] -propionic acid, [548] 2-methanesulfonylamino-3- [2- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -4,5-dihydro-oxazol-5-yl] -propionic acid, [549] 2-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4-methyl- 4,5-dihydro-oxazol-5-yl} -propionic acid, [550] 2-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4,5- Dihydro-thiazol-3-yl} -propionic acid, [551] 3-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4,5- Dihydro-3H-imidazol-4-yl} -propionic acid, and [552] 2- (2,6-Dichloro-benzoylamino) -3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -4,5-dihydro-oxazol-5-yl} -propionic acid is mentioned. [553] As a compound containing a moiety of the partial formula 1.1.1, [554] 3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4,5-dihydro -Oxazol-4-yl] -2-methyl-propionic acid, [555] 2-acetylamino-3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4 , 5-dihydro-oxazol-4-yl] -propionic acid, [556] 2-methanesulfonylamino-3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4,5-dihydro-oxazol-4-yl] -propionic acid, [557] 2,2-difluoro-3- {2- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- 4,5-dihydro-oxazol-4-yl} -propionic acid, [558] 2,2-dimethyl-3- [2- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -4,5- Dihydro-oxazol-4-yl] -propionic acid, [559] 2-allyloxycarbonylamino-3- {2-[({(3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4 , 5-dihydro-oxazol-4-yl} -propionic acid, [560] 2- (butane-1-sulfonylamino) -3- (2-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -4,5-dihydro-oxazol-4-yl) -propionic acid, [561] 2-Methyl-3- [2- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -4,5-dihydro-oxazole- 4-yl] -propionic acid, [562] 2-acetylamino-3- {2- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -4,5-dihydro-thiazol-4-yl} -propionic acid, [563] 2-methyl-3- (2- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -4,5-dihydro-oxazol-4-yl) Propionic acid, [564] 2-benzenesulfonylamino-3- (2- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -4,5-dihydro-oxazole-4- Yl) -propionic acid, [565] 2-benzenesulfonylamino-3- [2- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- 4,5-dihydro-oxazol-4-yl] -propionic acid, [566] 2-methanesulfonylamino-3- [2- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -4,5-dihydro-oxazol-4-yl] -propionic acid, [567] 2-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- 4,5-dihydro-oxazol-4-yl} -propionic acid, [568] 2-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4,5- Dihydro-thiazol-4-yl} -propionic acid, and [569] 2- (2,6-Dichloro-benzoylamino) -3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -4,5-dihydro-oxazol-4-yl} -propionic acid is mentioned. [570] Compounds comprising a moiety of the partial formula 1.1.2 [571] 3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -oxazol-5-yl ] -2-methyl-propionic acid, [572] 2-acetylamino-3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -oxa Sol-5-yl] -propionic acid, [573] 2-methanesulfonylamino-3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Oxazol-5-yl] -propionic acid, [574] 2,2-difluoro-3- {2- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Oxazol-5-yl} -propionic acid, [575] 2,2-Dimethyl-3- [2- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -oxazole-5 -Yl] -propionic acid, [576] 2-allyloxycarbonylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -oxa Sol-5-yl} -propionic acid, [577] 2- (butane-1-sulfonylamino) -3- (2-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -oxazol-5-yl) -propionic acid, [578] 2-Methyl-3- [2- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -oxazol-5-yl] -propionic acid, [579] 2-acetylamino-3- {2- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -thiazol-5-yl} -propionic acid, [580] 2-Methyl-3- (2- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-3-yl} -oxazol-5-yl) -propionic acid, [581] 2-benzenesulfonylamino-3- (2- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -oxazol-5-yl) -propionic acid, [582] 2-benzenesulfonylamino-3- [2- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Oxazol-5-yl] -propionic acid, [583] 2-methanesulfonylamino-3- [2- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -oxazol-5-yl] -propionic acid, [584] 2-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4-methyl- Oxazol-5-yl} -propionic acid, [585] 2-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -thiazole-5 -Yl} -propionic acid, [586] 3-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -3H-imidazole -4-yl} -propionic acid, and [587] 2- (2,6-Dichloro-benzoylamino) -3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -oxazol-5-yl} -propionic acid. [588] As a compound containing a moiety of the partial formula 1.1.3, [589] 3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl} -oxazol-4-yl ] -2-methyl-propionic acid, [590] 2-acetylamino-3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -oxa Zol-4-yl] -propionic acid, [591] 2-methanesulfonylamino-3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Oxazol-4-yl] -propionic acid, [592] 2,2-difluoro-3- {2- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Oxazol-4-yl} -propionic acid, [593] 2,2-dimethyl-3- [2- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -oxazole-4 -Yl] -propionic acid, [594] 2-allyloxycarbonylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -oxa Zol-4-yl} -propionic acid, [595] 2- (butane-1-sulfonylamino) -3- (2-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -oxazol-4-yl) -propionic acid, [596] 2-Methyl-3- [2- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -oxazol-4-yl] -propionic acid, [597] 2-formylamino-3- {2- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -thiazol-4-yl} -propionic acid, [598] 2-Methyl-3- (2- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -oxazol-4-yl) -propionic acid, [599] 2-benzenesulfonylamino-3- (2- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -oxazol-4-yl) -propionic acid, [600] 2-benzenesulfonylamino-3- [2- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Oxazol-4-yl] -propionic acid, [601] 2-methanesulfonylamino-3- [2- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -oxazol-4-yl] -propionic acid, [602] 2-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- Oxazol-4-yl} -propionic acid, [603] 2-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -thiazole-4 -Yl} -propionic acid, [604] 2- (2,6-Dichloro-benzoylamino) -3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -oxazol-4-yl} -propionic acid, [605] 3- [2- (1-{[4- (4-Chloro-benzyloxy) -3-fluoro-phenyl] -acetyl} -pyrrolidin-2-yl) -thiazol-5-yl] -propionic acid , [606] 3- [2- (1-{[3-Fluoro-4- (3-methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -thiazol-5-yl]- Propionic Acid, [607] 3- [2- (1-{[3-Chloro-4- (4-chloro-benzoyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -thiazol-5-yl] -propionic acid, [608] 3- [2- (1-{[4- (4-Chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -thiazol-5-yl] -propionic acid, [609] 3- (2- {1-[(4-benzyloxy-3-chloro-phenyl) -acetyl] -3-methyl-pyrrolidin-2-yl} -thiazol-5-yl) -propionic acid, [610] 3- [2- (1-{[4- (4-Chloro-benzyloxy) -phenyl] -acetyl} -3-methyl-pyrrolidin-2-yl) -thiazol-5-yl] -propionic acid, [611] 3- (2- {1-[(4-benzyloxy-phenyl) -acetyl] -3-methyl-pyrrolidin-2-yl} -thiazol-5-yl) -propionic acid, [612] 3- (2- {1-[(4-benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -thiazol-5-yl) -propionic acid, and [613] 3- (2- {1-[(4-benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid is mentioned. [614] Compounds containing residues of partial Formula 1.1.4 include [615] 3- [3- (1- (2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4,5-dihydro Isoxazol-5-yl] -2-methyl-propionic acid, [616] 2-acetylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4 , 5-dihydro-isoxazol-5-yl] -propionic acid, [617] 2-methanesulfonylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4,5-dihydro-isoxazol-5-yl] -propionic acid, [618] 2,2-difluoro-3- {3- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- 4,5-dihydro-isoxazol-5-yl} -propionic acid, [619] 2,2-dimethyl-3- [3- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -4,5- Dihydro-isoxazol-5-yl] -propionic acid, [620] 2-allyloxycarbonylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4 , 5-dihydro-isoxazol-5-yl} -propionic acid, [621] 2- (butane-1-sulfonylamino) -3- (3-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl) -acetyl) -amino] -methyl} -4,5-dihydro-isoxazol-5-yl) -propionic acid, [622] 2-Methyl-3- [3- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -4,5-dihydro-isoxazole- 5-yl] -propionic acid, [623] 2-formylamino-3- {3- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -4,5-dihydro-isothiazol-5-yl}- Propionic Acid, [624] 2-methyl-3- (3- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -4,5-dihydro-isoxazol-5-yl) Propionic acid, [625] 2-benzenesulfonylamino-3- (3- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -4,5-dihydro-isoxazole-5- Yl) -propionic acid, [626] 2-benzenesulfonylamino-3- [3- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- 4,5-dihydro-isoxazol-5-yl] -propionic acid, [627] 2-methanesulfonylamino-3- [3- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -4,5-dihydro-isoxazol-5-yl] -propionic acid, [628] 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4-methyl- 4,5-dihydro-isoxazol-5-yl) -propionic acid, [629] 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4,5- Dihydro-isothiazol-5-yl} -propionic acid, [630] 3-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -3,4- Dihydro-2H-pyrazol-3-yl} -propionic acid, and [631] 2- (2,6-Dichloro-benzoylamino) -3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -4,5-dihydro-isoxazol-5-yl} -propionic acid is mentioned. [632] Compounds containing residues of partial formula 1.1.5 [633] 3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4,5-dihydro -Pyrazol-1-yl] -2-methyl-propionic acid, [634] 2-acetylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4 , 5-dihydro-pyrazol-1-yl] -propionic acid, [635] 2-methanesulfonylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4,5-dihydro-pyrazol-1-yl] -propionic acid, [636] 2,2-difluoro-3- {3- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- 4,5-dihydro-pyrazol-1-yl} -propionic acid, [637] 2,2-dimethyl-3- [3- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -4,5- Dihydro-pyrazol-1-yl] -propionic acid, [638] 2- (butane-1-sulfonylamino) -3- (3-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -4,5-dihydro-pyrazol-1-yl) -propionic acid, [639] 2-Methyl-3- [3- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -4,5-dihydro-pyrazole- 1-yl] -propionic acid, [640] 2-acetylamino-3- {3- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -4,5-dihydro-pyrazol-1-yl} -propionic acid, [641] 2-methyl-3- (3- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -4,5-dihydro-pyrazol-1-yl) Propionic acid, [642] 2-benzenesulfonylamino-3- (3- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -4,5-dihydro-pyrazole-1- Il-propionic acid, [643] 2-benzenesulfonylamino-3- [3- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- 4,5-dihydro-pyrazol-1-yl] -propionic acid, [644] 2-methanesulfonylamino-3- [3- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -4,5-dihydro-pyrazol-1-yl] -propionic acid, [645] 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- 4,5-dihydro-pyrazol-yl} -propionic acid, [646] 2-formylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4,5 -Dihydro-pyrazol-1-yl} -propionic acid, and [647] 2- (2,6-Dichloro-benzoylamino) -3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -4,5-dihydro-pyrazol-1-yl} -propionic acid is mentioned. [648] Compounds comprising residues of partial formula 1.1.6 [649] 3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -isoxazole-5- General] -2-methyl-propionic acid, [650] 2-acetylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -isoxo Sazol-5-yl] -propionic acid, [651] 2-methanesulfonylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) Isoxazol-5-yl] -propionic acid, [652] 2,2-difluoro-3- {3- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Isoxazol-5-yl} -propionic acid, [653] 2,2-dimethyl-3- [3- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -isoxazole-5 -Yl] -propionic acid, [654] 2-allyloxycarbonylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl} -methyl] -methyl Sazol-5-yl} -propionic acid, [655] 2- (butane-1-sulfonylamino) -3- (3-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl) -acetyl) -amino] -methyl} -isoxazol-5-yl) -propionic acid, [656] 2-Methyl-3- [3- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [657] 2-acetylamino-3- {3- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -isothiazol-5-yl} -propionic acid, [658] 2-Methyl-3- (3- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, [659] 2-benzenesulfonylamino-3- (3- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, [660] 2-benzenesulfonylamino-3- [3- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Isoxazol-5-yl] -propionic acid, [661] 2-methanesulfonylamino-3- [3- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -isoxazol-5-yl] -propionic acid, [662] 2-formylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4-methyl Isoxazole-5-yl} -propionic acid, [663] 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -isothiazole- 5-yl} -propionic acid, [664] 3-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -2H-pyrazole -3-yl} -propionic acid, [665] 2- (2,6-Dichloro-benzoylamino) -3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -isoxazol-5-yl} -propionic acid, [666] 3- [3- (1-{[4- (pyridin-4-ylmethoxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [667] 3- [3- (1-{[4- (pyridin-3-ylmethoxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [668] 3- [3- (1-{[4- (pyridin-2-ylmethoxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [669] 3- (3- {1-[(6-benzyloxy-pyridin-3-yl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, [670] 3- (3- {1-[(5-benzyloxy-pyridin-2-yl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, [671] 3- (3- {1-[(4-benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -2-phenylamino-propionic acid, [672] 3- (3- {1-[(4-Benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -2- (pyridin-2-ylamino) -propionic acid , [673] 3- (3- {1-[(4-Benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -2- (pyridin-3-ylamino) -propionic acid , [674] 3- (3- {1-[(4-Benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -2- (pyridin-4-ylamino) -propionic acid , [675] 3- [3- (1-{[4- (5-Chloro-thiophen-2-ylmethoxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid , [676] 3- (3- {1-[(4-benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, [677] 3- (3- {1-{[4-Chloro-benzyloxy) -3-fluoro-phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [678] 3- [3- (1-{[3-Fluoro-4- (3-methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl]- Propionic Acid, [679] Phenyl]-(propane-1-sulfonylamino) -propionic acid, [680] 3- [3- (1-{[3-methoxy-4- (4-methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl]- Propionic Acid, [681] 3- [3- (1-{[3-methoxy-4- (3-methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl]- Propionic Acid, [682] 3- [3- (1-{[4- (4-Chloro-benzyloxy) -3-methoxy-phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid , [683] 3- [3- (1-{[4- (3-Chloro-benzyloxy) -3-methoxy-phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid , [684] 3- [3- (1-{[4- (2-Chloro-benzyloxy) -3-methoxy-phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid , [685] 3- [3- (1-{[4- (4-Fluoro-benzyloxy) -3-methoxy-phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl]- Propionic Acid, [686] 3- [3- (1-{[4- (3-Fluoro-benzyloxy) -3-methoxy-phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl]- Propionic Acid, [687] 3- [3- (1-{[4- (2-Fluoro-benzyloxy) -3-methoxy-phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl]- Propionic Acid, [688] 3- [3- (1-{[3-Chloro-4- (3-methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid , [689] 2-acetylamino-3- [3- (1-{[3-chloro-4- (3-methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazole-5 -Yl] -propionic acid, [690] 2-acetylamino-3- (3- {1-[(4-benzyloxy-3-methoxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, [691] 3- [3- (1-{[4- (5-tert-butyl- [1,2,4] oxadiazol-3-ylmethoxy) -phenyl] -acetyl} -pyrrolidin-2-yl) Isoxazol-5-yl] -propionic acid, [692] 2-acetylamino-3- [3- (1-{[3-chloro-4- (4-chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazole-5- General] -propionic acid, [693] 3- [3- (1-{[3-Chloro-4- (4-chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [694] 3- [3- (1-{[4- (2-Cyano-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [695] 3- [3- (1-{[4- (4-Cyano-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [696] 3- (3- {1-[(4-benzyloxy-3-fluoro-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, [697] 3- (3- {1-[(4-benzyloxy-3-chloro-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, [698] 3- (3- {1- [2- (4-benzyloxy-phenyl) -acetylamino] -3-methyl-butyl} -isoxazol-5-yl) -propionic acid, [699] 2-acetylamino-3- [3- (1-{[4- (3-cyano-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl]- Propionic Acid, [700] 2-acetylamino-3- [3- (1-{[4- (4-chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid , [701] 2-acetylamino-3- (3- {1-[(4-benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, [702] 3- (3- {1-[(4-p-tolyloxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, [703] 3- (3- {1-[(4-m-tolyloxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, [704] 3- (3- {1-[(4-o-tolyloxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, [705] 3- [3- (1-{(4- (4-Methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, [706] 3- [3- (1-{[4- (3-methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [707] 3- [3- (1-{(4- (2-Methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [708] 2-acetylamino-3- [3- (3-methyl-1- {2- [4- (2-methyl-benzyloxy) -phenyl] -acetylamino} -butyl) -isoxazol-5-yl]- Propionic Acid, [709] 2-acetylamino-3- (3- {1- [2- (4-benzyloxy-phenyl) -acetylamino] -3-methyl-butyl} -isoxazol-5-yl) -propionic acid, [710] 3- [3- (1-{[4- (4-Fluoro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [711] 3- [3- (1-{[4- (3-Fluoro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [712] 3- [3- (1-{[4- (2-Fluoro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [713] 3- [3- (1-{[4- (2-Chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [714] 3- [3- (1-{[4- (3-Chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [715] 3- [3- (1-{[4- (4-Chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [716] 3- [3- (1-{[4- (3-Methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [717] 3- [3- (1-{[4- (4-Methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [718] 3- [3- (1-{[4- (2-Methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [719] 3- (3- {3-Methyl-1- [2- (4-phenoxy-phenyl) -acetylamino] -butyl} -isoxazol-5-yl) -propionic acid, [720] 2-allyloxycarbonylamino-3- [3- (1-benzoyl-pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, [721] 3- (3- {1-[(4-benzyloxy-3-methoxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, [722] 3- (5- {1-[(4-benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -2H-pyrazol-3-yl) -propionic acid, and [723] 3- (3- {1- [3- {2-methyl-benzyloxy) -benzoyl] -pyrrolidin-2-yl) -isoxazol-5-yl) -propionic acid is mentioned. [724] Compounds comprising residues of partial formula 1.1.7 [725] 3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -pyrazol-1-yl ] -2-methyl-propionic acid, [726] 2-acetylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -pyra Zol-1-yl] -propionic acid, [727] 2-methanesulfonylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Pyrazol-1-yl] -propionic acid, [728] 2,2-difluoro-3- {3- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Pyrazol-1-yl} -propionic acid, [729] 2,2-dimethyl-3- [3- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -pyrazole-1 -Yl] -propionic acid, [730] 2- (butane-1-sulfonylamino) -3- (3-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -pyrazol-1-yl) -propionic acid, [731] 2-Methyl-3- [3- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -pyrazol-1-yl] -propionic acid, [732] 2-formylamino-3- {3- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -pyrazol-1-yl} -propionic acid, [733] 2-Methyl-3- (3- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -pyrazol-1-yl) -propionic acid, [734] 2-benzenesulfonylamino-3- (3- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -pyrazol-1-yl) -propionic acid, [735] 2-benzenesulfonylamino-3- [3- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Pyrazol-1-yl] -propionic acid, [736] 2-methanesulfonylamino-3- [3- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -pyrazol-1-yl] -propionic acid, [737] 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- Pyrazol-1-yl} -propionic acid, [738] 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -pyrazole-1 -Yl} -propionic acid, and [739] 2- (2,6-Dichloro-benzoylamino) -3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -pyrazol-1-yl} -propionic acid is mentioned. [740] As a compound containing a moiety of the partial formula 1.1.8, [741] 3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -oxazol-2-yl ] -2-methyl-propionic acid, [742] 2-acetylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -oxa Zol-2-yl] -propionic acid [743] 2-methanesulfonylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Oxazol-2-yl] -propionic acid, [744] 2,2-difluoro-3- {4- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Oxazol-2-yl} -propionic acid, [745] 2,2-dimethyl-3- [4- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -oxazole-2 -Yl] -propionic acid, [746] 2-allyloxycarbonylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -oxa Zol-2-yl} -propionic acid, [747] 2- (butane-1-sulfonylamino) -3- (4-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -oxazol-2-yl) -propionic acid, [748] 2-Methyl-3- [4- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -oxazol-2-yl] -propionic acid, [749] 2-formylamino-3- {4- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -thiazol-2-yl} -propionic acid, [750] 2-Methyl-3- (4- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -oxazol-2-yl) -propionic acid, [751] 2-benzenesulfonylamino-3- (4- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -oxazol-2-yl) -propionic acid, [752] 2-benzenesulfonylamino-3- [4- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Oxazol-2-yl] -propionic acid, [753] 2-methanesulfonylamino-3- [4- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -oxazol-2-yl] -propionic acid, [754] 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- Oxazol-2-yl} -propionic acid, [755] 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -thiazole-2 -Yl} -propionic acid, [756] 2- (2,6-Dichloro-benzoylamino) -3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -oxazol-2-yl} -propionic acid, and [757] 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -1 H-imidazole 2-yl} -propionic acid is mentioned. [758] Compounds comprising residues of partial formula 1.1.9 [759] 3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -imidazol-1-yl ] -2-methyl-propionic acid, [760] 2-acetylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -already Dazol-1-yl] -propionic acid, [761] 2-methanesulfonylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Imidazol-1-yl] -propionic acid, [762] 2,2-difluoro-3- {4- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Imidazol-1-yl} -propionic acid, [763] 2,2-dimethyl-3- [4- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -imidazole-1 -Yl] -propionic acid, [764] 2- (butane-1-sulfonylamino) -3- (4-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -imidazol-1-yl) -propionic acid, [765] 2-Methyl-3- [4- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -imidazol-1-yl] -propionic acid, [766] 2-formylamino-3- {4- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -imidazol-1-yl} -propionic acid, [767] 2-Methyl-3- (4- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -imidazol-1-yl) -propionic acid, [768] 2-benzenesulfonylamino-3- (4- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -imidazol-1-yl) -propionic acid, [769] 2-benzenesulfonylamino-3- [4- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Imidazol-1-yl] -propionic acid, [770] 2-methanesulfonylamino-3- [4- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -imidazol-1-yl] -propionic acid, [771] 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- Imidazol-1-yl} -propionic acid, [772] 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -imidazole-1 -Yl} -propionic acid, and [773] 2- (2,6-Dichloro-benzoylamino) -3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -imidazol-1-yl} -propionic acid is mentioned. [774] Compounds comprising residues of partial formula 1.1.10 [775] 3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl)-[1,2,4 ] Oxadiazol-5-yl] -2-methyl-propionic acid, [776] 2-acetylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl)-[ 1,2,4] oxadiazol-5-yl] -propionic acid, [777] 2-methanesulfonylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -[1,2,4] oxadiazol-5-yl] -propionic acid, [778] 2,2-difluoro-3- {3- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- [1,2,4] oxadiazol-5-yl} -propionic acid, [779] 2,2-dimethyl-3- [3- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl)-[1,2 , 4] oxadiazol-5-yl] -propionic acid, [780] 2-allyloxycarbonylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl]-[ 1,2,4] oxadiazol-5-yl} -propionic acid, [781] 2- (butane-1-sulfonylamino) -3- (3-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl}-[1,2,4] oxadiazol-5-yl) -propionic acid, [782] 2-methyl-3- [3- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl)-[1,2,4] oxadiazole -5-yl] -propionic acid, [783] 2-formylamino-3- {3- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl]-[1,2,4] thiadiazol-5-yl}- Propionic Acid, [784] 2-methyl-3- (3- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl}-[1,2,4] oxadiazol-5-yl ) -Propionic acid, [785] 2-benzenesulfonylamino-3- (3- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl}-[1,2,4] oxidazol-5 -Yl) -propionic acid, [786] 2-benzenesulfonylamino-3- [3- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- [1,2,4] oxadiazol-5-yl] -propionic acid, [787] 2-methanesulfonylamino-3- [3- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl)-[1,2,4] oxadiazol-5-yl] -propionic acid, [788] 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl- [1,2, 4] oxadiazol-5-yl} -propionic acid, [789] 2-formylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl]-[1, 2,4] thiadiazol-5-yl} -propionic acid, [790] 3-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -2H- [1 , 2,4] thiazol-3-yl} -propionic acid, and [791] 2- (2,6-Dichloro-benzoylamino) -3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl]-[1,2,4] oxadiazol-5-yl} -propionic acid. [792] A compound comprising a moiety of partial formula 1.1.11 [793] 3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl)-[1,2,4 ] Triazol-1-yl] -2-methyl-propionic acid, [794] 2-acetylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl)-[ 1,2,4] triazol-1-yl] -propionic acid, [795] 2-methanesulfonylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -[1,2,4] triazol-1-yl] -propionic acid, [796] 2,2-difluoro-3- {3- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- [1,2,4] triazol-1-yl} -propionic acid, [797] 2,2-dimethyl-3- [3- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl)-[1,2 , 4] triazol-1-yl] -propionic acid, [798] 2-allyloxycarbonylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl]-[ 1,2,4] triazol-1-yl} -propionic acid, [799] 2- (butane-1-sulfonylamino) -3- (3-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl}-[1,2,4] triazol-1-yl) -propionic acid, [800] 2-Methyl-3- [3- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl)-[1,2,4] triazole- 1-yl] -propionic acid, [801] 2-acetylamino-3- {3- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl]-[1,2,4] triazol-1-yl} -propionic acid, [802] 2-methyl-3- (3- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl}-[1,2,4] triazol-1-yl) Propionic acid, [803] 2-benzenesulfonylamino-3- (3- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl}-[1,2,4] triazole-1- Yl) -propionic acid, [804] 2-benzenesulfonylamino-3- [3- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- [1,2,4] triazol-1-yl] -propionic acid, [805] 2-methanesulfonylamino-3- [3- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl)-[1,2,4] triazol-1-yl] -propionic acid, [806] 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4-methyl- [1,2,4] triazol-1-yl} -propionic acid, [807] 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl]-[1,2 , 4] triazol-1-yl} -propionic acid, and [808] 2- (2,6-Dichloro-benzoylamino) -3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl]-[1,2,4] triazol-1-yl} -propionic acid is mentioned. [809] Compounds comprising moieties of the partial formula 1.1.12 [810] 3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -thiophen-2-yl ] -2-methyl-propionic acid, [811] 2-acetylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -furan -2-yl] -propionic acid, [812] 2-methanesulfonylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Thiophen-2-yl] -propionic acid, [813] 2,2-difluoro-3- {4- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- 1H-pyrrole-2-yl} -propionic acid, [814] 2,2-Dimethyl-3- [4- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -thiophene-2 -Yl] -propionic acid, [815] 2- (butane-1-sulfonylamino) -3- (4-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -furan-2-yl) -propionic acid, [816] 2-Methyl-3- [4- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -1 H-pyrrol-2-yl] -propionic acid , [817] 2-formylamino-3- [4- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -thiophen-2-yl} -propionic acid, [818] 2-Methyl-3- (4- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -1 H-pyrrol-2-yl) -propionic acid, [819] 2-benzenesulfonylamino-3- (4- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -furan-2-yl) -propionic acid, [820] 2-benzenesulfonylamino-3- [4- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Thiophen-2-yl] -propionic acid, [821] 2-methanesulfonylamino-3- [4- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -1H-pyrrol-2-yl] -propionic acid, [822] 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- 1H-pyrrole-2-yl} -propionic acid, [823] 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -thiophene-2 -Yl} -propionic acid, and [824] 2- (2,6-Dichloro-benzoylamino)-{4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl ] -Furan-2-yl} -propionic acid is mentioned. [825] Compounds having residues of partial formula 1.1.13 [826] 3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -thiophen-3-yl ] -2-methyl-propionic acid, [827] 2-acetylamino-3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -furan -3-yl] -propionic acid, [828] 2-methanesulfonylamino-3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Thiophen-3-yl] -propionic acid, [829] 2,2-difluoro-3- {5- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- 1H-pyrrole-3-yl} -propionic acid, [830] 2,2-dimethyl-3- [5- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -thiophene-3 -Yl] -propionic acid, [831] 2- (butane-1-sulfonylamino) -3- (5-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -furan-3-yl) -propionic acid, [832] 2-Methyl-3- [5- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -1 H-pyrrol-3-yl] -propionic acid , [833] 2-formylamino-3- {5- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -thiophen-3-yl} -propionic acid, [834] 2-Methyl-3- (5- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -1 H-pyrrol-3-yl-propionic acid, [835] 2-benzenesulfonylamino-3- (5- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -furan-3-yl) -propionic acid, [836] 2-benzenesulfonylamino-3- [5- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Thiophen-3-yl] -propionic acid, [837] 2-methanesulfonylamino-3- [5- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -1H-pyrrol-3-yl] -propionic acid, [838] 2-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -2-methyl- 1H-pyrrole-3-yl} -propionic acid, [839] 2-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -thiophene-3 -Yl} -propionic acid, and [840] 2- (2,6-Dichloro-benzoylamino) -3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -furan-3-yl} -propionic acid is mentioned. [841] Compounds comprising residues of partial formula 1.1.14 [842] 3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -thiophen-2-yl ] -2-methyl-propionic acid, [843] 2-acetylamino-3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -furan -2-yl] -propionic acid, [844] 2-methanesulfonylamino-3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Thiophen-2-yl] -propionic acid, [845] 2,2-difluoro-3- {5- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- 1H-pyrrole-2-yl} -propionic acid, [846] 2,2-dimethyl-3- [5- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -thiophene-2 -Yl] -propionic acid, [847] 2- (butane-1-sulfonylamino) -3- (5-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -furan-2-yl) -propionic acid, [848] 2-Methyl-3- [5- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -1 H-pyrrol-2-yl] -propionic acid , [849] 2-formylamino-3- {5- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -thiophen-2-yl} -propionic acid, [850] 2-Methyl-3- (5- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -1 H-pyrrol-2-yl) -propionic acid, [851] 2-benzenesulfonylamino-3- (5- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -furan-2-yl) -propionic acid, [852] 2-benzenesulfonylamino-3- [5- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Thiophen-2-yl] -propionic acid, [853] 2-methanesulfonylamino-3- [5- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -1H-pyrrol-2-yl] -propionic acid, [854] 2-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -2-methyl- 1H-pyrrole-2-yl} -propionic acid, [855] 2-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -thiophene-2 -Yl} -propionic acid, and [856] 2- (2,6-Dichloro-benzoylamino) -3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -furan-2-yl} -propionic acid is mentioned. [857] Compounds comprising residues of partial formula 1.1.15 [858] 3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -isoxazol-3-yl ] -2-methyl-propionic acid, [859] 2-acetylamino-3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -isoxo Sazol-3-yl] -propionic acid, [860] 2-methanesulfonylamino-3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) Isoxazol-3-yl] -propionic acid, [861] 2,2-difluoro-3- {5- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Isoxazol-3-yl} -propionic acid, [862] 2,2-dimethyl-3- [5- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -isoxazole-3 -Yl] -propionic acid, [863] 2-allyloxycarbonylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -isolate Sazol-3-yl} -propionic acid, [864] 2- (butane-1-sulfonylamino) -3- (5-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -isoxazol-3-yl) -propionic acid, [865] 2-Methyl-3- [5- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-3-yl] -propionic acid, [866] 2-acetylamino-3- {5- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -isothiazol-3-yl} -propionic acid, [867] 2-Methyl-3- (5- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-3-yl) -propionic acid, [868] 2-benzenesulfonylamino-3- (5- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-3-yl) -propionic acid, [869] 2-benzenesulfonylamino-3- [5-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazole- 3-yl] -propionic acid, [870] 2-methanesulfonylamino-3- [5- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -isoxazol-3-yl] -propionic acid, [871] 2-formylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4-methyl Isoxazol-3-yl} -propionic acid, [872] 2-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -isoxazole- 3-yl} -propionic acid, [873] 3-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -2H-pyrazole -5-yl} -propionic acid, and [874] 2- (2,6-Dichloro-benzoylamino) -3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -isoxazol-3-yl} -propionic acid is mentioned. [875] Compounds comprising residues of partial formula 1.1.16 [876] 3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -oxazol-2-yl ] -2-methyl-propionic acid, [877] 2-acetylamino-3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -oxa Zol-2-yl] -propionic acid, [878] 2-methanesulfonylamino-3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Oxazol-2-yl] -propionic acid, [879] 2,2-difluoro-3- {5- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Oxazol-2-yl} -propionic acid, [880] 2,2-Dimethyl-3- [5- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -oxazole-2 -Yl] -propionic acid, [881] 2-allyloxycarbonylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl} -methyl] -oxa Zol-2-yl} -propionic acid, [882] 2- (butane-1-sulfonylamino) -3- (5-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -oxazol-2-yl) -propionic acid, [883] 2-Methyl-3- [5- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -oxazol-2-yl] -propionic acid, [884] 2-formylamino-3- {5- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -thiazol-2-yl} -propionic acid, [885] 2-Methyl-3- (5- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -oxazol-2-yl) -propionic acid, [886] 2-benzenesulfonylamino-3- (5- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -oxazol-2-yl) -propionic acid, [887] 2-benzenesulfonylamino-3- [5- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Oxazol-2-yl] -propionic acid, [888] 2-methanesulfonylamino-3- [5- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -oxazol-2-yl] -propionic acid, [889] 2-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- Oxazol-2-yl} -propionic acid, [890] 2-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -thiazole-2 -Yl} -propionic acid, [891] 2- (2,6-Dichloro-benzoylamino) -3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -oxazol-2-yl} -propionic acid, and [892] 2-acetylamino-3- [5-({2- [4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -methyl) -1 H-imidazol-2-yl] -propionic acid Can be mentioned. [893] Compounds comprising residues of partial formula 1.1.17 [894] 3- (5- {1-[(4-benzyloxy-3-methoxy-phenyl) -acetyl] -pyrrolidin-2-yl}-[1,3,4] thiadiazol-2-yl) Propionic acid, [895] 3- [5- (1-{[4- (4-chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl)-[1,3,4] thiadiazol-2-yl ] -Propionic acid, and [896] 3- (5- {1-[(4-benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl}-[1,3,4] thiadiazol-2-yl) -propionic acid is mentioned. have. [897] Compounds comprising residues of partial formulas 1.1.18, 1.1.19 and 1.1.20 [898] 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -phenyl} -propionic acid , [899] 2-formylamino-3- {6- [1-({3-methoxy-4- [3- (3-methyl-pyridin-2-yl) -ureido] -phenyl} -acetyl) -pyrroli Din-2-yl] -pyridin-2-yl} -propionic acid, [900] 3- [4- [1-({3-ethyl-4- [3- (3-methyl-pyridin-2-yl) -ureido] -phenyl} -acetyl) -pyrrolidin-2-yl]- Pyrimidin-2-yl} -propionic acid, [901] 2-acetylamino-3- [3- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl) -phenyl] Propionic acid, [902] 2-acetylamino-3- [3-({2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -methyl) -phenyl] -propionic acid, [903] 2- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -pyridin-4-ylmethyl} -4 Methyl-pentanoic acid, [904] 3- {2-[(Methyl-{[4- (3-o-tolyl-ureido) -phenyl] -acetyl} -amino) -methyl] -pyridin-4-yl} -propionic acid, [905] 2-methanesulfonylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl]-[1 , 3,5] triazin-2-yl} -propionic acid, [906] 1- [4- (1-{[6- (3-Pyridin-2-yl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -pyridin-2-ylmethyl ] -Cyclopropanecarboxylic acid, [907] 3- [3- (1-{[6- (3-Pyridin-2-yl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -phenyl] -butyl acid, [908] 2- (butane-1-sulfonylamino) -3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino)- Methyl] -phenyl} -propionic acid, [909] 2-benzenesulfonylamino-3- [3-({[(2-methoxy-2'-methyl-biphenyl-4-yl) -acetyl] -methyl-amino} -methyl) -phenyl] -propionic acid, [910] 2- (3-{[2- (4-benzyloxy-phenyl) -acetylamino] -methyl} -benzyl) -malonic acid, [911] 2- [3-({2- [4- (4-Chloro-benzyloxy) -phenyl] -acetylamino} -methyl) -benzyl] -malonic acid, [912] 3- [3-({2- [4- (3-Fluoro-benzyloxy) -phenyl] -acetylamino} -methyl) -phenyl] -2- (propane-1-sulfonylamino) -propionic acid, [913] 3- [3-({2- [3-Chloro-4- (4-chloro-benzyloxy) -phenyl] -acetylamino} -methyl) -phenyl] -2- (propane-1-sulfonylamino)- Propionic Acid, [914] 3- (3-{[2- (4-benzyloxy-3-chloro-phenyl) -acetylamino] -methyl} -phenyl) -2- (propane-1-sulfonylamino) -propionic acid, [915] 3- [3-({2- [4- (3-Chloro-benzyloxy) -phenyl] -acetylamino} -methyl) -phenyl] -2- (propane-1-sulfonylamino) -propionic acid, [916] 3- [3-({2- [4- (4-Chloro-benzyloxy) -phenyl] -acetylamino} -methyl) -phenyl] -2- (propane-1-sulfonylamino) -propionic acid, [917] 3- (3-{[2- (4-benzyloxy-3-methoxy-phenyl) -acetylamino] -methyl} -phenyl) -2- (propane-1-sulfonylamino) -propionic acid, [918] 3- (3-{[2- [4- (4-Methyl-benzyloxy) -phenyl] -acetylamino} -methyl) -2-acetylamino-3- (3-{[2- (4-benzyloxy -Phenyl) -acetylamino] -methyl} -phenyl) -propionic acid, [919] 3- (3-{[2- (4-benzyloxy-phenyl) -acetylamino] -methyl} -phenyl) -2- (propane-1-sulfonylamino) -propionic acid, [920] 2- (propane-1-sulfonylamino) -3- {3-[(2-m-tolyl-acetylamino) -methyl] -phenyl} -propionic acid, [921] 3- (3-{[2- (4-hydroxymethyl-phenyl) -acetylamino] -methyl} -phenyl) -2- (propane-1-sulfonylamino) -propionic acid, and [922] 3- [3- (phenylacetylamino-methyl) -phenyl] -2- (propane-1-sulfonylamino) -propionic acid is mentioned. [923] Compounds comprising residues of partial formula 1.1.21 [924] 3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -pyrrol-1-yl] 2-methyl-propionic acid, [925] 2-acetylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -pyrrole -1-yl] -propionic acid, [926] 2-methanesulfonylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Pyrrol-1-yl] -propionic acid, [927] 2,2-difluoro-3- {4- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Pyrrole-1-yl} -propionic acid, [928] 2,2-dimethyl-3- [4- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -pyrrole-1- General] -propionic acid, [929] 2- (butane-1-sulfonylamino) -3- (4-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -pyrrol-1-yl) -propionic acid, [930] 2-Methyl-3- [4- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -pyrrole-1-yl] -propionic acid, [931] 2-formylamino-3- {4- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -pyrrole-1-yl} -propionic acid, [932] 2-Methyl-3- (4- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -pyrrole-1-yl) -propionic acid, [933] 2-benzenesulfonylamino-3- (4- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -pyrrole-1-yl) -propionic acid, [934] 2-benzenesulfonylamino-3- [4- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Pyrrole-1-yl] -propionic acid, [935] 2-methanesulfonylamino-3- [4- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -pyrrole-1-yl] -propionic acid, [936] 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- Pyrrole-1-yl} -propionic acid, [937] 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -pyrrole-1- General-propionic acid, and [938] 2- (2,6-Dichloro-benzoylamino) -3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -pyrrol-1-yl} -propionic acid is mentioned. [939] Compounds comprising moieties of the partial formula 1.1.22 [940] 3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -pyrazol-1-yl ] -2-methyl-propionic acid, [941] 2-acetylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -pyra Zol-1-yl] -propionic acid, [942] 2-methanesulfonylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Pyrazol-1-yl] -propionic acid, [943] 2,2-difluoro-3- [4- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Pyrazol-1-yl} -propionic acid, [944] 2,2-Dimethyl-3- [4- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -pyrazole-1 -Yl] -propionic acid, [945] 2- (butane-1-sulfonylamino) -3- (4-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -pyrazol-1-yl) -propionic acid, [946] 2-Methyl-3- [4- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -pyrazol-1-yl] -propionic acid, [947] 2-formylamino-3- {4- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -pyrazol-1-yl} -propionic acid, [948] 2-Methyl-3- (4- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -pyrazol-1-yl) -propionic acid, [949] 2-benzenesulfonylamino-3- (4- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -pyrazol-1-yl) -propionic acid, [950] 2-benzenesulfonylamino-3- [4- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Pyrazol-1-yl] -propionic acid, [951] 2-methanesulfonylamino-3- [4- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -pyrazol-1-yl] -propionic acid, [952] 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- Pyrazol-1-yl} -propionic acid, [953] 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -pyrazole-1 -Yl} -propionic acid, and [954] 2- (2,6-Dichloro-benzoylamino) -3- {4-{({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -pyrazol-1-yl} -propionic acid is mentioned. [955] Compounds comprising moieties of the partial formula 1.1.23 [956] 2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -benzooxazole-6-carboxylic acid, [957] 2- [1- (2- {3-methoxy-4- [3- (3-methyl-pyridin-2-yl) -ureido] -phenyl} -acetylamino) -3-methyl-butyl] -3H -Benzoimidazole-5-carboxylic acid, [958] 2- (1-{[4- (3-pyridin-2-yl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl) -1 H-imidazole [4,5-c] pyridine- 6-carboxylic acid, [959] 2- (1-{[3-Ethoxy-4- (3-pyridin-2-yl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl) -benzothiazole-6-carboxylic acid, [960] 2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -benzothiazole-6-carboxylic acid, [961] 2-({[(4-benzyloxy-phenyl) -acetyl] -methyl-amino} -methyl) -oxazole [5,4-b] pyridine-5-carboxylic acid, and [962] 3-methyl-2- {1-[(4-phenoxy-phenyl) -acetyl] -pyrrolidin-2-yl} -3H-benzoimidazole-5-carboxylic acid is mentioned. [963] The aforementioned compounds of the present invention may be used in the form of acids, esters, or other classes of compounds to which the aforementioned compounds belong. It is also within the scope of the present invention to use such compounds in the form of pharmaceutically acceptable salts derived from various organic and inorganic acids and bases according to methods known in the art. Such known pharmaceutically acceptable salts include acetates, adipates, alginates, aspartates, benzoates, benzenesulfonates, besylates, bisulfates, butyrates, citrate, camphorates, camphorsulfonates, cyclopentanes Propionate, digluconate, dodesulfate, ethanesulfonate, fumarate, glucoheptanoate, gluconate, glycerophosphate, hemisuccinate, hemisulfate, heptanoate, hexanoate, hypofurate, Hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethanesulfonate, isethionate, lactate, lactobionate, maleate, mandelate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, Nitrate, oxalate, oleate, pamoate, pectinate, persulfate, 3-phenylprop Cypionate, Phosphonate, Picrate, Pivalate, Propionate, Salicylate, Sodium Phosphate, Stearate, Succinate, Sulfate, Sulfosalicylate, Tartrate, Thiocyanate, Thiomalate, Tosylate , And undecanoate, although not limited thereto. [964] Base salts of the compounds of the invention include ammonium salts; Alkali metal salts such as sodium and potassium, alkaline earth metal salts such as calcium and magnesium; Salts with organic bases such as dicyclohexylamine, meglumine, N-methyl-D-glucamine, tris- (hydroxymethyl) -methylamine (trimetamine); Salts with amino acids such as arginine, lysine, and the like, but are not limited thereto. Compounds of the present invention comprising basic nitrogen-containing groups include (C 1 -C 4 ) alkyl halides such as methyl, ethyl, iso-propyl and tert-butyl chloride, bromide and iodide; Di (C 1 -C 4 ) alkyl sulfates such as dimethyl, diethyl and diamyl sulfates; (C 10 -C 18 ) alkyl halides such as decyl, dodecyl, lauryl, myristyl and stearyl chloride, bromide and iodide; And aryl- (C 1 -C 4 ) alkyl halides such as benzyl chloride and phenethyl bromide. Such salts make both the water soluble compound and the oil soluble compound of the present invention possible. [965] Among the pharmaceutically acceptable salts mentioned above, preferred salts are acetate, mesylate, citrate, fumarate, gluconate, hemisuccinate, hypofulate, hydrochloride, hydrobromide, isothionate, mandelate, meglu Min, nitrate, oleate, phosphonate, pivalate, sodium phosphate, stearate, sulfate, sulfosalicylate, tartrate, thiomalate, tosylate and trimethylamine. [966] In the case of compounds of the present invention having one or more groups capable of forming such pharmaceutically acceptable salts, polyvalent salts are formed, which are also included in the scope of the present invention. Examples of forms of typical polyvalent salts include, but are not limited to, bitartrate, diacetate, difumarate, dimeglumine, diphosphate, disodium, and trihydrochloride. [967] The pharmaceutical composition of the present invention may be prepared by the preparation of one or more of the above-described inhibitor compounds according to the present invention or a pharmaceutically acceptable salt as described above, depending on the properties and expected performance of the carriers known in the art. It can be included with. [968] As used herein, the term "carrier" includes acceptable diluents, excipients, adjuvants and vehicles. Pharmaceutically acceptable carriers that can be used in the pharmaceutical compositions of the invention include ion exchange compositions; Alumina; Aluminum stearate; Lecithin; Serum proteins such as human serum albumin; Phosphate; Glycine; Sorbic acid; Potassium sorbate; Partial glyceride mixtures of saturated vegetable fatty acids; water; Salts or electrolytes such as proramine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride and zinc salts; Colloidal silica; Magnesium trisilicate; Polyvinyl pyrrolidone; Cellulosic materials such as sodium carboxymethylcellulose; Polyethylene glycol; Polyacrylates; Wax; Polyethylene-polyoxypropylene-block polymers, and wool fats, but are not limited thereto. [969] More specifically, diluents, excipients, adjuvants and vehicles used in the pharmaceutical compositions of the present invention include oxidizing agents, such as acetic acid, glacial acetic acid, malic acid and propionic acid, added to achieve a desired or predetermined pH; And alkalizing agents such as edetol, potassium carbonate, potassium hydroxide, sodium borate, sodium carbonate, and sodium hydroxide; Propellants for nebulizers, for example acceptable halogenated hydrocarbons, which are required when the pharmaceutical composition is administered as a nebulizer under significant pressure; nitrogen; Or volatile hydrocarbons such as butane, propane, isobutane or mixtures thereof; Antimicrobial agents, including antibiotics, antifungal and antiprotozoal agents, added when the pharmaceutical composition is administered topically, for example antimicrobials such as benzyl alcohol, chlorobutanol, phenylethyl alcohol, phenylmercuric acetate, potassium sorbate, and sorbent Acid and antifungal agents such as benzoic acid, butylparaben, ethylparaben, methylparaben, propylparaben and sodium benzoate; Antimicrobial preservatives added to pharmaceutical compositions, such as alkyl esters of p-hydroxybenzoic acid, propionate salts, phenoxyethanol, methylparaben sodium, propylparaben sodium, to protect the pharmaceutical composition from the growth of potentially harmful microorganisms. Sodium dehydroacetate, benzalkonium chloride, benzethium chloride, and benzyl alcohol; Antioxidants such as anoxomers, ascorbyl palmitate, butylated hydroxyanisole, added to protect all components of the pharmaceutical composition from damage or degradation by acidifying agents present in the pharmaceutical composition itself or in the environment of use, Butylated hydroxytoluene, hypophosphorous acid, potassium metabisulfite, propyl octyl and dodecyl gallate, sodium metabisulfite, sulfur dioxide, and tocophenols; Buffers used to maintain the desired pH of the pharmaceutical compositions once prepared, such as potassium acetate, potassium metaphosphate, potassium phosphate monobesic, and tartaric acid, and tartaric acid, and assist in maintaining the ionic strength of the pharmaceutical compositions and decomposing compounds and metals Chelates for the effective removal of e.g. edetate disodium, ideate disodium, and edetic acid. [970] Skin active agents are added to the pharmaceutical compositions of the invention for topical administration, for example wound healing agents such as peptide derivatives, enzymes, panthenol, hexylesorcinol, phenol, tetracycline hydrochloride, lamin and kinetin; Glucocorticosteroids for the treatment of inflammation, for example hydrocortisone, dexamethasone, betamethasone, triamcinolone, fluorocinolone and methylprednisolone; Retinoids for the treatment of acne, psoriasis, skin aging and skin cancer, such as retinol, tretinoin, isotretinoin, ethretinate, acitretin, and arotinoids, immunosuppressive agents for treating inflammation such as dapson and sulfasalazine; Weak antibacterial agents, such as resorcinol, ralylic acid, benzoyl peroxide, erythromycin-benzoyl peroxide, erythromycin, clindamycin, and mupirosine, antifungal agents such as gliofulvin, azoles, for example micron Azoles, econazoles, itraconazoles, fluconazoles, and ketoconazoles, and allylamines such as naphthypine and terpinapine, antiviral agents such as acylclovir, famcyclovir, and valacyclo Vir, antihistamines, for example diphenylhydramine, terpenadine, astemizol, rollatadine, cetirizine, acrivastin, and temelastin, local anesthetics such as benzocaine, lidocaine, dibucaine, and pra Pan hydrochloride, topical analgesics such as methyl salylsilate, camphor, menthol, and resorcinol; Topical preservatives to prevent infections such as benzalkonium chloride and povidone-iodine; Vitamins and derivatives thereof such as tocopherol, tocopherol acetate, retinic acid and retinol. [971] In addition, examples of the diluents, excipients, adjuvants and vehicles used in the pharmaceutical compositions of the present invention include dispersants and suspending agents such as polyzinane, povidone, and silicon dioxide; Emollients, e.g., hydrocarbon oils and waxes, triglyceride esters, acetylated monoglycerides, C 10 -C 20 fatty acid methyl and other alkyl esters, C 10 -C 20 fatty acids, C 10 -C 20 fatty alcohols, lanolin And derivatives, polyhydric alcohol esters such as polyethylene glycol (200-600), polyoxyethylene sorbitan fatty acid esters, wax esters, phospholipids, and sterols; Emulsifiers used for the preparation of oil-in-water emulsions; Excipients such as laurocampram and polyethylene glycol monomethyl ether; Wetting agents such as sorbitol, glycerin and hyaluronic acid; Ointment bases such as waselin, polyethylene glycol, lanolin, and poloxamer; Penetration enhancers such as dimethyl isosorbide, diethyl-glycol-monoethylether, 1-dodecylazacycloheptan-2-one, and dimethylsulfoxide (DMSO); Preservatives such as benzalkonium chloride, benzethonium chloride, alkyl esters of p-hydroxybenzoic acid, hydantoin derivatives, cetylpyridinium chloride, propylparaben, quaternary ammonium compounds such as potassium benzoate, and tee Merosal; Osteogolizing agents including cyclodextrins, for example acetone, alcohols, amylene hydrate, butyl alcohol, corn oil, cottonseed oil, ethyl acetate, glycerin, hexylene glycol, isopropyl alcohol, isostearyl alcohol, methyl alcohol, methylene chloride Mineral oil, peanut oil, phosphoric acid, polyethylene glycol, polyoxypropylene 15 stearyl ether, propylene glycol, propylene glycol diacetate, sesame oil, and distilled water; Stabilizers such as calcium saccharide and thymol; Surfactants such as rapylium chloride; Laureth 4, ie, α-dodecyl-ω-hydroxy-poly (oxy-1,2-ethanediyl) or polyethylene glycol monododecyl ether. [972] According to the invention, the pharmaceutical composition may be in the form of a sterile injectable preparation, for example, an aqueous or oily suspension for sterile injection. Such suspensions can be prepared according to techniques known in the art using suitable dispersing or wetting agents and suspending agents. Sterile injectable preparations may also be sterile injectable solutions or suspensions of diluents or solvents acceptable for nontoxic-parenteral administration, such as, for example, solutions of 1,3-butanediol. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil may be employed including synthetic monoglycerides or di-glycerides. Fatty acids such as oleic acid and their glyceride derivatives are useful for the preparation of pharmaceutically acceptable natural oils such as olive oil or castols, especially in the form of polyoxyethylates thereof, injectables. Such oil solutions or suspensions may also contain long chain alcohol diluents or dispersants, for example Rh, HClX or similar alcohols. [973] The pharmaceutical compositions of the present invention may be orally administered in any orally acceptable dosage form including, but not limited to, capsules, tablets, aqueous suspensions or solutions. In the case of tablets for oral use, carriers commonly used include lactose and corn starch. Lubricants such as magnesium stearate are also typically added. For oral administration in a capsule form, useful diluents include lactose and anhydrous corn starch. If an aqueous suspension is required for oral use, the active ingredient is mixed with the emulsifier and suspending agent. If desired, certain sweetening, flavoring or complexing agents may also be added. Alternatively, the pharmaceutical composition of the present invention may be administered in the form of suppositories for rectal administration. They may be prepared by mixing the medicament with a suitable harmless excipient which is solid at room temperature or liquid at rectal temperature and will therefore dissolve in the rectum to release the drug. Such materials include cocoa butter, beeswax and polyethylene glycols. [974] In addition, the pharmaceutical compositions of the present invention may be administered topically when the site of treatment is a region or organ readily accessible by topical application, for example in the case of diseases of the eye, skin or lower gastrointestinal tract. Suitable topical formulations are readily prepared for each of these areas or organs. [975] Topical administration for the lower gastrointestinal tract may be carried out in the form of rectal suppositories or suitable enema preparations as described above. Topically active skin patches can also be used. [976] For topical administration, the pharmaceutical composition may be formulated in the form of a suitable ointment containing the active ingredient suspended or dissolved in one or more carriers. Carriers for topical administration of the compounds of the present invention include, but are not limited to, mineral oil, liquid waselin, white waselin, propylene glycol, polyoxyethylene, polyoxypropylene compounds, emulsifying waxes and water. Alternatively, the pharmaceutical composition may be formulated in a suitable lotion or cream containing the active ingredient suspended or dissolved in one or more pharmaceutically acceptable carriers. Suitable carriers include, but are not limited to, mineral oil, sorbitan monostearate, polysorbate, cetyl ester wax, cetaryl alcohol, 2-octyldodecanol, benzyl alcohol and water. [977] For ophthalmic use, the pharmaceutical composition may be formulated in a finely divided suspension in isotonic pH controlled sterile saline, or preferably in a solution in isotonic pH controlled sterile saline, with or without preservatives such as benzylalkonium chloride. have. Optionally, for ophthalmic use, the pharmaceutical composition may be formulated in an ointment such as waselin. [978] The pharmaceutical compositions of the invention may also be administered by the use of a nebulizer, a dry powder inhaler or a metered dose of inhaler or nasal aerosol. Such compositions are prepared according to techniques known in the pharmaceutical formulating art, using benzyl alcohol or other suitable preservatives, absorption enhancers that improve bioavailability, hydrofluorocarbons and / or other conventional solubilizers or dispersants. It can be prepared in saline solution. [979] The amount of active ingredient that can be mixed with the carrier material to produce a single dosage form will depend upon the subject to be treated and the particular mode of administration. However, specific dosages and treatment regimens for any particular patient may vary depending on the activity, age, weight, general health, sex, diet, time of administration, rate of release, combination of drugs, and severity of the particular disease to be treated and the specific compound used. It will depend on many factors, including your doctor's judgment. In addition, the amount of active ingredient will depend on the therapeutic and prophylactic drugs, if such ingredients are present together. [980] The dosages and rates of administration of the compounds of the invention that are effective in preventing, inhibiting, controlling or alleviating the inevitable or related pathogenesis subsequently mediated by cell adhesion and VLA-4 can be determined by the nature of the inhibitor, the size of the patient, the therapeutic purpose. It will depend on various factors such as the nature of the pathogen to be treated, the specific pharmaceutical composition used, and the observations and judgments of the treating physician. [981] For example, if the dosage form is oral administration, eg a tablet or capsule, a suitable dosage form of the compound of formula 1.0.0 may be from about 1.0 μg / kg body weight to about 10.0 mg / kg body weight of active ingredient per day. ), Preferably from about 5.0 μg / weight (kg) to about 5.0 mk / weight (kg), more preferably from about 10.0 μg / weight (kg) to about 1.0 mg / weight (kg), most preferably about From 20.0 μg / kg body weight to 0.5 mg / kg body weight. [982] When the dosage form is topical administration to the bronchus and lungs, for example using powder inhalers or nebulizers, a suitable dosage of the compound of formula 1.0.0 may be from about 0.1 μg / kg body weight of the active ingredient per day. About 1.0 mg / weight (kg), preferably about 0.5 μg / weight (kg) to about 0.5 mg / weight (kg), more preferably about 1.0 μg / weight (kg) to about 1.0 mg / weight (kg ), Most preferably from about 2.0 μg / kg body weight to about 0.05 mg / kg body weight. [983] When representative weights of 10 kg and 100 kg are used to illustrate the range of daily topical dosages used as described above, a suitable dosage of the compound of formula 1.0.0 is from about 1.0-10.0 μg to 10.0- per day 100.0 mg, preferably about 5.0-50.0 μg to 5.0-50.0 mg, more preferably about 10.0-100.0 μg to 1.0-10.0 mg, most preferably about 20.0-200.0 μg to about 0.5 to 5.0 mg of formula 1.0 .0 compound. Doses in this range represent the total dose of active ingredient per day for the set patient. Dosages per day will depend on pharmacological and pharmacokinetic factors, such as the half-life of the active ingredient, when administering a dose, which is minimal and optimal for those active ingredients in patients requiring their metabolic rate and clearance and therapeutic efficacy. Reflect content in plasma or other body fluids. [984] Various other factors should be considered in determining the number of doses per day and the amount of active ingredient per dose to be administered. The most important of these other factors is the individual response to the patient to be treated. Thus, for example, if the active ingredient is used to treat or prevent asthma and is topically administered to the lungs by aerosol inhalation, one to four times per day consisting of the operation of a "puff" of the dispersing device, ie the inhaler. Administration will be performed and each dose will contain from about 50.0 μg to about 10.0 mg of active ingredient. [985] Essentially anti-inflammatory corticosteroids in addition to the compounds of the present invention being the active ingredient; Bronchodilators; Asthma treatments; Non-steroidal anti-inflammatory agents; Immunosuppressants; Immune stimulants; Anti-metabolites; Embodiments comprising a composition containing as an active ingredient an additional therapeutically active ingredient selected from the group consisting of psoriasis and diabetes treatments are also within the scope of the present invention. Specific compounds of this class are described in Comprehensive Medicinal Chemistry, Pergamon Press, Oxford, England, pp. 970-986 (1990; and Goodman and Gilman's the Pharmacological Basis of Therapeutics, 9th ed., Hardman, JG and Limbird, LE, ed., Harman, JG and Limbird, LE, eds., McGraw-Hill, 1996). Particularly preferred active ingredients included for use with the compounds of Formula 1.0.0 include anti-inflammatory compounds such as theophylline, sulfasalazine and aminosalicylates; cyclosporine, FK-506 and rapha. Immunosuppressive agents such as mycin, anti-metabolites such as cyclophosphamide and methotrexate, and immunomodulators such as interferon. [986] This aspect of the invention relates to a method of treating or preventing inflammatory, autoimmune or respiratory diseases by inhibiting cell adhesion and subsequent or related onset processes mediated by VLA-4. As mentioned above, VLA-4 related cell adhesion plays an important role in various inflammatory diseases, autoimmune diseases and autoimmune diseases. Thus, inhibition of cell adhesion by the compounds of the present invention can be used in methods of treating or preventing inflammatory diseases, immune diseases and autoimmune diseases. Preferably, the disease to be treated by the method of the present invention is selected from asthma, arthritis, psoriasis, transplant rejection, multiple sclerosis, diabetes and inflammatory bowel disease. [987] The above-described treatment method of the present invention may use the compound of Formula 1.0.0 in the form of a monotherapy, but the method uses one or more compounds of Formula 1.0.0 as known anti-inflammatory agents, immunomodulators, immune stimulants or immunosuppressants. It can be used in the form of multiple therapies co-administered with. The term "co-administered" or "co-administered" as used herein is intended to mean the therapeutic use of one or more compounds of Formula 1.0.0 with an additional one or more therapeutic agents, the same or different administration. Administration of a mixture of therapeutically active ingredients in a single dosage form or multiple dosage forms representing a route, but is not intended to be limiting, where the multiple dosage forms can be administered simultaneously or sequentially at different time points. Can be. [988] Subsequent to the synthesis of the aforementioned preferred species of the present invention or any other compound falling within the scope of the present invention, the biological activity associated with the VLA-4 specificity of the compound is determined in vitro and in vivo as set forth in the technical literature of the art. As a test method, it can be measured using one or more species. For example, some of the latest assays and models measure VLA-4 activity by measuring the concentration of test candidate inhibitors required to inhibit the binding of VLA-4 expressing cells to fibronectin- or CS-1 coated plates. It is related to doing. In this assay, microtinter wells are coated with fibronectin (containing the CS-1 sequence), CS-1 peptide or soluble VCAM-1. When coated in the wells, various concentrations of test compound are then added together with suitably labeled VLA-4 expressing cells. Optionally, test compounds were added first and incubated in coated wells before being added to the cells. The cells were incubated in the wells for at least 30 minutes. After incubation, the wells were emptied and washed. Binding inhibition is measured by quantifying the fluorescence or radioactivity bound to the plate for each of the various concentrations of the test compound and a control that does not contain the test compound. However, the assays described in this way are less desirable than the other assays described further below to determine the VLA-4 activity of the compounds of Formula 1.0.0. [989] VLA-4 expressing cells that can be used in this assay include Ramos cells, Jurkat cells, A375 melanoma cells, and human peripheral vascular lymphocytes (PBL). Cells used in this assay can be fluorescent or radiolabelled. [990] In order to analyze the VLA-4 inhibitory specificity of the test compound, an analysis of the main groups of integrins, namely β 2 and β 3 and other β 1 integrins such as VLA-5, VLA-6 and α 4 β 7 Can be done. Such assays may be similar to the direct binding assay described above, which inhibits adhesion and substitutes appropriate integrin-expressing cells and corresponding ligands. For example, multinucleated cells (PMN) express β 2 integrins on their surface and bind to ICAM, while β 3 integrins are involved in platelet aggregation and inhibition may be assessed by standard platelet aggregation assays. VLA-5 specifically binds to the Arg-Gly-Asp sequence, while VLA-6 binds to laminin. In addition, α 4 β 7 is a recently discovered homologue of VLA-4 and binds to fibronectin and VCAM and MAdCAM-1. α 4 β specificity to 7, for cell line, for example, expressing the CS-1, VCAM or α 4 β 7 non-MAdCAM-1, and VLA-4 is measured by the binding assay method using RPMI-8866 cells . [991] Once VLA-4 specific inhibitors have been identified, they can be further characterized by in vivo assays. Such assays are described in Henderson et al., "Blockade of CD49d (α 4 integrin) on intrapulmonary by not circulating leukocytes inhibits airway inflammation and hyperresponsiveness in a mouse model of asthma", J. Clin. Invest., 100 (12), pp. 3083-92 (1997), test for allergen-induced airway hypersensitivity and cell influx. In this assay, mice are sensitized by ip exposure to stimulants such as ovalbumin. After the recovery period, mice were infected by aerosol exposure to allergens. Prior to aerosol exposure, mice were given various doses of VLA-4 inhibitors by intratracheal injection. In vivo inhibition of cell adhesion-related inflammation is assessed by measuring the number of cells and cytokines in bronchoalveolar lavage fluid. In this method, the inhibitors of the present invention that are most suitable for inhibiting inflammation can be found. [992] Another in vivo assay that can be used is the primate asthma assay. Such assays are described in Turner, C. R. et al., "Characterization of a primate model of asthma using anti-allergy / anti-asthma agents", Inflammation Research, 45 (5), pp. 239-45 (1996). This assay measures the inhibition of allergic primate Ascaris antigen-induced late airway and airway hyperresponsiveness following administration of anti-allergic / anti-asthmatic drugs. [993] The compounds of the present invention may be provided as pharmaceutical compositions that can be administered orally or orally via inhalation (in a dosed dose of inhaler, dry powder inhaler or nebulizer), topical, rectal, nasal, eye, buccal, vaginal or transplant reservoir. It may be. The term "parenteral" as used herein refers to subcutaneous, intravenous, intramuscular, intraarticular, intramuscular, intrasternal, intradural, intrahepatic, intralesional and intracranial injection or infusion techniques. Include. [994] Compounds of Formula 1.0.0 can be prepared according to known methods for carrying out the synthesis of organic compounds which are naturally nonpeptide-based or semipeptidyl. Many different methods that are fully described in the technical literature and are familiar to those skilled in the art are useful. The technical content following many of these synthetic schemes is not intended to be limiting. Many abbreviations have been used to save space. These abbreviations are already known to the skilled person, but are described below for clarity and convenience: [995] BOP: benzotriazol-1-yloxy-tris (dimethylamino) phosphonium hexafluorophosphate; [996] EDCl: 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride; [997] DAST: diethylaminosulfur trifluoride; [998] HOBT: 1-hydroxybenzotriazole; [999] DIEA: diisopropylethyl amine; [1000] THF: tetrahydrofuran; [1001] DMF: Dimethylformamide. [1002] Step A of Synthesis Scheme 1 [1003] [1004] Synthesis of a compound of Formula 1.0.0 in which the “B” component is an isoxazole ring and the “Y” component is —SO 2 — is illustrated in Steps A to G of Scheme 1. In step A of Scheme 1, the starting material diethyl amino malonate is commercially available, for example, from Aldrich Chemical Company, Milwaukee, 53233 Wisconsin. Amide products (2.0.1) wherein R 5 is hydrogen, methyl or phenyl are also commercially available. R 5 is alkyl, aryl, heterocyclyl or heteroaryl, and other amides literature [March, J. "Advanced Organic Chemistry ", 3 rd edition, 1985] Suitable using fully described the conditions for acid chloride with an amine (2.0 It can be obtained easily by reacting .0). Similar conditions can be used to convert the amine (2.0.0) to its corresponding sulfonamide by reaction of the amine (2.0.0) with an alkyl or aryl sulfonyl chloride. Carbamate products (2.0.1) wherein R 5 is alkoxy or aryloxy are described in Paik, Yi Hyon; Dowd, Paul; J. Org. Chem. 1986, 51 (15), 2910-2913 and Kawai, Masao; Nyfeler, Rolf; Berman, Judd M .; Goodman, Murray; J. Med. Chem. , 1982 25 (4), 397-402, prepared from amines (2.0.0). [1005] Step B of Synthetic Scheme 1 [1006] [1007] In step B of Scheme 1, intermediate (2.0.3) is prepared from oxime (2.0.2). Oxime (2.0.2) is a procedure well known to those skilled in the art from its corresponding aldehydes (see, eg, Chung, Yong Jun; Ryu, Eun Jung; Keum, Gyochang; Kim, Byeang Hyean: Bioorg. Med. Chem . ; 1996, 4 (2) 209-226 and Kim, Byeang Hyean; Chung, Yong Jun; Keum, Gyochang; Kim, Jaheon; Kim, Kimoon; Tetrahedron Lett . ; 1992, 33 (45) 6811-6814]). Oxime (2.0.2) is oxidized in a suitable solvent such as THF, chloroform or methylene chloride by a suitable oxidizing agent such as sodium hypochlorite, t-butyl hypochlorite or N-chlorosuccinimide and the resulting nitrile N- The oxide is converted to isoxazole (2.0.3) by reacting with propargyl bromide in situ. Such [2 + 3] ring addition reactions are well known in the literature as a method for preparing isoxazole ring structures. See, eg, Synthesis , 508-9, 1982. [1008] Step C of Synthetic Scheme 1 [1009] [1010] In step C of Scheme 1, the bromide intermediate (2.0.3) is converted to isoxazole containing component (2.0.4). Bromide (2.0.3) is reacted with malonate (2.0.1) optionally substituted in a suitable solvent such as DMF, DMSO or methylene chloride in the presence of a base such as triethylamine or cerium carbonate. DMF is the preferred solvent and cerium carbonate is the preferred base. The reaction is carried out at a temperature of 0 to 30 ° C. for 1 to 16 hours. The reaction of bromide (2.0.3) with malonate (2.0.1) in step C of Scheme 1 is not limited to 2-amino malonate and is of formula [EtOC (= 0) CHR 7 C (= 0) OEt] It can be expanded to include malonates, wherein R 7 is as defined for Formula 1.0.0. [1011] Step D of Synthetic Scheme 1 [1012] [1013] The synthesis of the mono ester intermediate (2.0.5) is illustrated in step D of Scheme 1. Conversion of diethyl malonate (2.0.4) into a half-ester intermediate by reaction with a suitable equivalent of base such as sodium hydroxide or lithium hydroxide in a solvent such as THF, methanol, t-butanol or dioxane Let's do it. Preference is given to using aqueous sodium hydroxide in dioxane. The reaction is carried out at a temperature of 0-50 ° C. for 1-16 hours. 3 hours at ambient temperature is preferred. The semi-ester intermediate is then transformed into mono ester (2.0.5) in situ by heating in a suitable solvent such as benzene, toluene or dioxane at a temperature of 0-200 ° C. for 1-16 hours. Preference is given to heating in dioxane at 125 ° C. for 3 hours. [1014] Step E of Synthetic Scheme 1 [1015] [1016] The synthesis of the amine intermediate (2.0.6) is illustrated in step E of Scheme 1. The t-butyloxycarbamate intermediate (2.0.5) is reacted with a solution of hydrochloric acid in a suitable non-aqueous solvent such as dioxane or an acid such as pure trifluoroacetic acid. The reaction is carried out at a temperature of 0-50 ° C. for 1-16 hours. Hydrochloric acid in dioxane for 1 hour at ambient temperature is the preferred condition. Those skilled in the art will appreciate that t-butyloxycarbonyl groups act as protecting groups for amines and other suitable protecting groups may be used. It will also be appreciated that the method of removing such protecting groups must be compatible with all functional groups present in R 5 . Such methods are well known in the technical literature of the art. See, eg, Greene, TW, Wuts, PGM Protective Group in Organic Synthesis ; John Wiley & Sons: New York, 1991. [1017] Step F of Synthetic Scheme 1 [1018] [1019] The synthesis of sulfonamide intermediates (2.0.7) is described in step F of Scheme 1. The amine (2.0.6) may be substituted with sulfonyl chloride in a solvent such as dichloromethane, water or pyridine with or without a base such as sodium carbonate or diisopropylethylamine, wherein A (CH 2 ) n-SO 2 Cl, wherein "A" and "n" are as defined for Formula 1.0.0]. The reaction is carried out at 0-50 ° C. for 1-16 hours. Preferred conditions are sodium carbonate in water for 16 hours at ambient temperature. [1020] Step G of Synthetic Scheme 1 [1021] [1022] The carboxylic acid product is prepared from ester intermediate (2.0.7) as illustrated in step G of Scheme 1. The ester intermediate (2.0.7) is reacted with a suitable aqueous base such as lithium hydroxide, potassium hydroxide or sodium hydroxide in a solvent such as t-butanol, methanol and / or THF. The reaction is carried out at a temperature of 0-50 ° C. for 0.5-24 hours. Aqueous lithium hydroxide in a mixture of THF and methanol for 1 hour at ambient temperature is a preferred condition. [1023] The above-described synthesis can be applied broadly to the compound of formula 1.0.0. To make this synthesis clearer, steps A to G of the following synthetic scheme 1-α are shown for certain compounds of the present invention. [1024] Synthetic Scheme 1-α [1025] [1026] The schematic synthetic diagram below illustrates a general process for the preparation of compounds of Formula 1.0.0 in which the “Y” component is C═O. [1027] Step A of Synthesis Scheme 2 [1028] [1029] Starting material A 1 -NCO is an isocyanate whose definition for “A 1 ” is the same as the definition for component A of Formula 1.0.0 for aryl, heteroaryl and heterocyclyl moieties substituted with 0 to 3 R 9 . . Isocyanate starting materials for preparing component A, such as phenyl isocyanate, o-tolyl isocyanate, 2-fluorophenyl isocyanate and 2-chlorophenyl isocyanate, are commercially available from Aldrich Chemical Company, Milwaukee, 53233, Wisconsin. Alternatively, isocyanate starting materials can be readily prepared using the methods described from their corresponding amines in the literature [March, J., "Advanced Organic Chemistry" 3 rd edition, 1985]. The pyridyl analogs of the phenyl isocyanates can be used to prepare the corresponding compounds of formula 1.0.0 in which the A component contains pyridyl groups. [1030] One of the aforementioned isocyanates is reacted with an amine of formula 2.0.10. Adding amines to isocyanates is a well known reaction that provides substituted urea in an easy manner. The reaction can be carried out in a solvent such as methylene chloride using triethylamine at slightly elevated temperatures. Subsequently, the disubstituted urea (2.0.11) prepared by the above-described scheme, which forms a reactant that produces component A of the compound of formula 1.0.0, is reacted with an amine of formula "-NR 4 CR 2 R 3 -B", Wherein “B” is as defined in one of Formulas 1.1.0 to 1.1.22. [1031] Step B of Synthetic Scheme 2 [1032] [1033] The reaction between the component A forming reactant (2.0.11) and the amine (2.0.6) is carried out at a room temperature or slightly higher temperature, for example a coupling agent such as 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydro Chloride (EDCl) and 1-hydroxybenzotriazole (HOBT), dicyclohexylcarbodiimide (DCCI), N, N'-carbonyldiimidazole, N, N, N ', N'-tetramethyl (succinate Imido) amine of amine with carboxylic acid which can proceed in excellent yield by use of uronium tetrafluoroborate and benzotriazol-1-yloxy-tris (dimethylamino) phosphonium hexafluorophosphate (BOP) Reactions involving misfire will be recognized by those skilled in the art. The amine component (2.0.6) can be obtained as described in Scheme 1. The reaction can be exemplified by the above schematic synthetic diagram providing a general process for the preparation of the compound of formula 1.0.0. [1034] In order to prepare the final product of formula 1.0.0 in acid form, an additional step as shown in the following scheme is required. [1035] Step C of Synthetic Scheme 2 [1036] [1037] The final acid product (2.0.13) is prepared from ester (2.0.12) as illustrated in the scheme above. The intermediate is reacted with a suitable aqueous hydroxide base such as lithium hydroxide, potassium hydroxide or sodium hydroxide in a solvent system consisting of t-butanol, methanol or THF and methanol. The reaction is carried out at a temperature of 0-50 ° C. for 0.5-16 hours. Lithium hydroxide in THF, methanol and water for 1 hour at ambient temperature is the preferred condition. [1038] The above-described synthesis can be applied broadly to the compound of formula 1.0.0. To make this synthesis more clear, steps A through C of the following synthetic scheme 2-a are shown for certain compounds of the invention. [1039] Synthetic Scheme 2-α [1040] [1041] Other synthesis of the compound of Formula 1.0.0 is illustrated in steps A to C of Synthesis Scheme 3. The synthesis of amine intermediate (2.0.4) is illustrated in step A of Scheme 3. The t-butyloxycarbamate intermediate (2.0.4) is reacted with a solution of hydrochloric acid in a suitable non-aqueous solvent such as dioxane or an acid such as pure trifluoroacetic acid. The reaction is carried out at a temperature of 0-50 ° C. for 1-16 hours. Hydrochloric acid in dioxane for 1 hour at ambient temperature is the preferred condition. Those skilled in the art will appreciate that t-butyloxycarbonyl groups act as protecting groups for amines and other suitable protecting groups may be used. It will also be appreciated that the method of removing such protecting groups must be compatible with all functional groups present in R 5 . Such methods are well known in the technical literature of the art. See, eg, Greene, TW, Wuts, PGM Protective Group in Organic Synthesis ; John Wiley & Sons: New York, 1991. [1042] Step A of Synthesis Scheme 3 [1043] [1044] Step B of Synthetic Scheme 3 [1045] [1046] In step B of Scheme 3, the amine (2.0.14) is reacted with acid (2.0.15) under the same conditions as step B of Synthesis Scheme 2. [1047] In order to prepare the final product of formula 1.0.0 in acid form, an additional step as shown in the following scheme is required. [1048] Step C of Synthetic Scheme 3 [1049] [1050] The final acid product (2.0.17) is prepared from ester (2.0.16) as illustrated in the scheme above. The intermediate is reacted with a suitable aqueous hydroxide base such as lithium hydroxide, potassium hydroxide or sodium hydroxide in a solvent system consisting of t-butanol, methanol or THF and methanol. The reaction is carried out at a temperature of 0-50 ° C. for 0.5-16 hours. Lithium hydroxide in THF, methanol and water for 1 hour at ambient temperature is the preferred condition. [1051] The above-described synthesis can be applied broadly to the compound of formula 1.0.0. To make this synthesis clearer, steps A to C of the following synthetic schemes 3-α are shown for certain compounds of the invention. [1052] Synthetic Scheme 3-α [1053] [1054] Other ways for the synthesis of compounds of Formula 1.0.0 are illustrated in steps A through D of Synthetic Scheme 4. [1055] Step A of Synthesis Scheme 4 [1056] [1057] In step A of Scheme 4, oxime (2.0.2) is oxidized by a suitable oxidizing agent such as sodium hypochlorite, t-butyl hypochlorite or N-chlorosuccinimide in a suitable solvent such as THF, chloroform or methylene chloride. And the resulting nitrile N-oxide is converted to isoxazole (2.0.18) by reacting with 2,2-disubstituted methyl pent-4-inoate in situ. Such [2 + 3] ring addition reactions are well known in the literature as a method for producing isoxazole ring structures. See, eg, Synthesis , 508-9, 1982. [1058] Step B of Synthetic Scheme 4 [1059] [1060] The synthesis of amine intermediate (2.0.19) is illustrated in the above scheme using the same conditions as in step A of Scheme 3. Starting material is t-butyloxycarbamate intermediate (2.0.18). [1061] Step C of Synthetic Scheme 4 [1062] [1063] In step C of Scheme 4, the amine (2.0.19) is reacted with acid (2.0.15) under the same conditions as step B of Synthetic Scheme 2. The reaction can be exemplified by the above schematic synthetic diagram providing a general process for the preparation of the compound of formula 1.0.0. [1064] In order to prepare the final product of formula 1.0.0 in acid form, an additional step as shown in the following scheme is required. [1065] Step D of Synthetic Scheme 4 [1066] [1067] The final acid product (2.0.21) was prepared from ester (2.0.20) as illustrated in the above scheme using the method of Step C of Scheme 3. [1068] The above-described synthesis can be applied broadly to the compound of formula 1.0.0. To make this synthesis clearer, steps A to C of the following synthetic schemes 4-α are shown for certain compounds of the invention. [1069] Synthetic Scheme 4-α [1070] [1071] Other ways for the synthesis of compounds of Formula 1.0.0 are illustrated in steps A through D of Synthetic Scheme 5. [1072] Step A of Synthesis Scheme 5 [1073] [1074] Bromide (2.0.22) is commercially available from Aldrich Chemical Company, Milwaukee, 53233, Wisconsin. The bromide (2.0.22) is converted to the desired diester containing component (2.0.23) as shown in the above scheme. The bromide is reacted with amino malonate under the conditions described in step C of Scheme 1. [1075] Step B of Synthetic Scheme 5 [1076] [1077] Nitrile (2.0.23) is converted to the desired amine (2.0.24) as illustrated in the above scheme. As the nitrile (2.0.23) described in the literature [March, J. "Advanced Organic Chemistry ", 3 rd edition, 1985] is reduced to the amine (2.0.24) by corresponding to the hydrogen addition. [1078] The above-described synthesis can be applied broadly to the compound of formula 1.0.0. To make this synthesis clearer, the following synthetic scheme 5-a is presented. [1079] Synthetic Scheme 5-α [1080] [1081] Synthesis of the bicyclic compound of Formula 1.0.0 is illustrated in steps A-D of Synthesis Scheme 6. Starting materials are, for example, acids and amines commercially available from Aldrich Chemical Company, Milwaukee, 53233, Wisconsin. [1082] Step A of Synthesis Scheme 6 [1083] [1084] The reactions exemplified in the above schemes can be carried out at room temperature or slightly higher temperatures such as coupling agents such as 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride (EDCl) and 1-hydroxybenzotriazole (HOBT). ), Dicyclohexylcarbodiimide (DCCI), N, N'-carbonyldiimidazole, POCl 3 , TiCl 4 , SO 2 ClF, Ti (OBu) 4 , P 2 I 4 , Bu 3 N, benzotriazole -1-yl diethyl phosphate, N, N, N ', N'-tetramethyl (succinimido) uronium tetrafluoroborate and preferably di-iso-propylethyl amine (DIEA) and benzotriazole- Acylation of amine (2.0.22) with carboxylic acid (2.0.23), which can proceed in excellent yield by the use of 1-yloxy-tris (dimethylamino) phosphonium hexafluorophosphate (BOP) Reactions will be appreciated by those skilled in the art. [1085] Step B of Synthetic Scheme 6 [1086] [1087] The synthesis of amine intermediate (2.0.26) is illustrated in the above scheme. The starting material is a mixture of t-butyloxycarbamate intermediates (2.0.24) and (2.0.25). Intermediates (2.0.24) and (2.0.25) are reacted with an acid, such as hydrochloric acid or acetic acid, with or without a suitable solvent such as dioxane. The reaction is carried out at 0-100 ° C. for 1-16 hours. Acetic acid is preferred in the absence of additional solvent at 80 ° C. for 1.5 hours. It will be appreciated by those skilled in the art that the above conditions can achieve both cyclization and removal of t-butyloxycarbonyl groups to form the desired bicyclic system. It will also be appreciated by those skilled in the art that t-butyloxycarbonyl groups act as protecting groups for amines and other suitable protecting groups can be used. It will also be appreciated that the method of removing such protecting groups must be compatible with all functional groups present in the intermediate (2.0.26). Such methods are well known in the technical literature of the art. See, eg, Greene, TW, Wuts, PGM Protective Group in Organic Synthesis ; John Wiley & Sons: New York, 1991. [1088] The above-described synthesis can be applied broadly to the compound of formula 1.0.0. To make this synthesis clearer, the following synthetic scheme 6-α is shown for certain compounds of the invention. [1089] Synthetic Scheme 6-α [1090] [1091] Another way for the synthesis of compounds of Formula 1.0.0 is illustrated in steps A to C of Synthesis Scheme 7. The above steps describe different routes to component B used in the coupling reaction as described in step B of Synthetic Scheme 2. [1092] Step A of Synthesis Scheme 7 [1093] [1094] Preparation of the bromide intermediate (2.0.29) was described in step A of Synthesis Scheme 1. Intermediate bromide (2.0.29) is suitable in the presence of additives such as tetrabutyl ammonium bromide, tetrabutyl ammonium chloride or tetraphenylammonium bromide with a base such as cesium carbonate, cesium hydroxide or potassium hydroxide, such as toluene, methylene chloride or DMF. Reaction with commercial imine (2.0.30) in a solvent. The reaction was carried out for 1 to 16 hours at a temperature of -78 to 50 ° C. The reaction of imine (2.0.30) and bromide intermediate (2.0.29) in toluene in the presence of tetrabutylammonium bromide for 1 hour at ambient temperature is preferred. [1095] Step B of Synthetic Scheme 7 [1096] [1097] The synthesis of amine intermediate (2.0.32) is illustrated in the above scheme. Amine intermediates (2.0.31) can be transformed into amines (2.0.32) by various methods well known to those skilled in the art and described in the literature. See, eg, Wolfe, John P .; Ahman, Jens; Sadighi, Joseph P .; Singer, Robert A .; Buchwald, Stephen L .; Tetrahedron Lett. ; 1997, 38 (36); 6367-6370 and Corey, EJ; Xu, Feng .; Noe, Mark C .; J. Am. Chem, Soc. , 1997, 119, 12414-12415. In a preferred method, intermediate imine (2.0.31) is treated with a mixture of ethyl acetate and hydrochloric acid at ambient temperature for 3 hours. [1098] Step C of Synthetic Scheme 7 [1099] [1100] The synthesis of amide intermediate (2.0.33) is illustrated in the above scheme. Regardless of the presence or absence of a solvent such as dichloromethane, chloroform, benzene, water or pyridine, the amine is reacted with acid anhydride or acid chloride with or without the addition of a base such as sodium carbonate, pyridine or diisopropyl ethyl amine. The reaction is carried out at a temperature of 0 to 50 ° C. for 1 to 16 hours. Preferred conditions are the use of dichloromethane and pyridine for 16 hours at ambient temperature. [1101] The above-described synthesis can be applied broadly to the compound of formula 1.0.0. To make this synthesis clearer, the following synthetic scheme 7-α is shown. [1102] Synthetic Scheme 7-α [1103] [1104] Examples of Preferred Embodiments [1105] The following examples further illustrate the compounds, compositions, and methods of treatment of the invention, but are not intended to limit the scope of the invention thereto. Many abbreviations are used in the following examples because they occupy much space. These abbreviations are well known to those skilled in the art, but are presented below to aid the reader in understanding: [1106] BOP: Benzotriazol-1-yloxy-tris (dimethylamino) phosphonium hexafluorophosphate [1107] DAST: diethylaminosulfur trifluoride [1108] DIEA: diisopropylethyl amine [1109] DMF: Dimethylformamide [1110] EDCI: 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride [1111] HOBT: 1-hydroxybenzotriazole [1112] THF: Tetrahydrofuran [1113] Example 1 [1114] A. 2-allyloxycarbonylamino-3- {3- [1- (3,5-dichloro-benzenesulfonyl) -pyrrolidin-2-yl] -isoxazol-5-yl} -propionic acid [1115] [1116] 2-allyloxycarbonylamino-3- {3- [1- (3,5-dichloro-benzenesulfonyl) -pyrrolidin-2-yl] -isoxazol-5-yl} -propionic acid ethyl ester (59 mg , 0.108 mmol) of tetrahydrofuran (1.0 mL) and methanol (0.5 mL) solution was stirred with 2 M aqueous lithium hydroxide (0.5 mL) at room temperature for 40 minutes. The reaction was acidified to pH 1 with 1 M hydrochloric acid and extracted twice with ethyl acetate. The combined extracts were dried over magnesium sulfate and concentrated in vacuo to afford the title compound as a white solid (51 mg, 91%). MS (CI) m / z 518 (M + l). [1117] B. 2-allyloxycarbonylamino-3- {3- [1- (3,5-dichloro-benzenesulfonyl) -pyrrolidin-2-yl] -isoxazol-5-yl} -propionic acid ethyl ester [1118] [1119] 2-allyloxycarbonylamino-3- (3-pyrrolidin-2-yl-isoxazol-5-yl) -propionic acid ethyl ester hydrochloride (110 mg, 0.294 mmol) and sodium carbonate (93.5 mg, 0.882 mmol) Was dissolved in water (1.5 mL) and 3,5-dichlorobenzenesulfonylchloride (86.7 mg, 0.353 mmol) was added. The mixture was stirred overnight. The reaction was extracted twice with dichloromethane. The combined organics were washed with brine, dried over magnesium sulfate and concentrated in vacuo to afford the title compound (59 mg, 37%). MS (CI) m / z 545.7 (M + l). [1120] C. 2-allyloxycarbonylamino-3- (3-pyrrolidin-2-yl-isoxazol-5-yl) -propionic acid ethyl ester hydrochloride [1121] [1122] 2- [5- (2-allyloxycarbonylamino-2-ethoxycarbonyl-ethyl) -isoxazol-3-yl] -pyrrolidine-1-carboxylic acid t-butyl ester (3.44 g, 7.86 mmol) Was dissolved in 4M hydrochloric acid in dioxane (10 mL) and stirred at room temperature for 2 hours. The reaction was then concentrated in vacuo and co-evaporated with dichloromethane to afford the desired product as a brown waxy solid. MS (CI) m / z 509.9 (M + 1) [1123] D. 2- [5- (2-allyloxycarbonylamino-2-ethoxycarbonyl-ethyl) -isoxazol-3-yl] -pyrrolidine-1-carboxylic acid t-butyl ester [1124] [1125] 2-allyloxycarbonylamino-2- [3- (1-t-butoxycarbonyl-pyrrolidin-2-yl) -isoxazol-5-ylmethyl] -malonic acid monoethyl ester with 2-allyl Oxycarbonylamino-2- [3- (1-t-butoxycarbonyl-pyrrolidin-2-yl) -isoxazol-5-ylmethyl] -malonic acid diethyl ester (10.4 g, 21.5 mmol) Was dissolved in dioxane (130 mL) and heated to 125 ° C. for 3 h in an oil bath. Dioxane was then removed under vacuum. The residue was dissolved in ethyl acetate, washed with saturated sodium carbonate and brine, dried over magnesium sulfate and concentrated. The crude material was chromatographed on a Biotage Flash 40M column eluting with ethyl acetate / hexanes (1: 4) to give the title compound as a clear oil (5.12 g, 56% step 2). MS (CI) m / z 338.0 (M-99). 2-allyloxycarbonylamino-2- [3- (1-t-butoxycarbonyl-pyrrolidin-2-yl) -isoxazol-5-ylmethyl] -malonic acid diethyl ester was recovered ( 2.96 g, 27%). MS (CI) m / z 509.9 (M + 1), 409.9 (M-99). [1126] E. 2-allyloxycarbonylamino-2- [3- (1-t-butoxycarbonyl-pyrrolidin-2-yl) -isoxazol-5-ylmethyl] -malonic acid monoethyl ester [1127] [1128] 1 M sodium hydroxide (21.5 mL, 21.5 mmol) was dissolved in 2-allyloxycarbonylamino-2- [3- (1-t-butoxycarbonyl-pyrrolidin-2-yl) -isoxazol-5-yl To a solution of dioxane (22 mL) of methyl] -malonic acid diethyl ester (10.95 g, 21.5 mmol) was added in part over 30 minutes. After stirring overnight, the reaction was not complete. An additional 0.2 equivalents of 1 M sodium hydroxide (4.2 mL, 4.2 mmol) was added and stirring continued for 3 hours. The reaction was diluted with ethyl acetate (50 mL) and 1 M sulfuric acid (23 mL) was added dropwise at 0 ° C. The aqueous portion was extracted twice with ethyl acetate. The combined organics were dried over magnesium sulfate and concentrated in vacuo to afford the title compound. The crude product was used directly in next step without separation of unreacted diester. MS (CI) m / z 382.2 (M-99). [1129] F. 2-allyloxycarbonylamino-2- [3- (1-t-butoxycarbonyl-pyrrolidin-2-yl) -isoxazol-5-ylmethyl] -malonic acid diethyl ester [1130] [1131] 2- (5-Bromomethyl-isoxazol-3-yl) -pyrrolidine-1-carboxylic acid t-butyl ester (7.29 g, 56 mmol) with 2-allyloxycarbonylamino-malonic acid diethyl ester (8.25 g, 32 mmol) of dimethyl formamide (260 mL) solution was cooled to 0 ° C. and cesium carbonate (25.41 g, 78 mmol) was added. The reaction was allowed to warm to room temperature and stirred for 3 hours. The reaction mixture was then poured into diethyl ether (2 L) and washed with water (5 x 200 mL) and brine. The organic portion was dried over magnesium sulfate and concentrated in vacuo. The crude residue was chromatographed on silica gel eluting with ethyl acetate: hexanes (3: 7) to afford the title compound as a clear colorless oil (10.95 g, 83%). MS (CI) m / z 260.1 (M-99). [1132] G. 2-allyloxycarbonylamino-malonic acid diethyl ester [1133] [1134] A solution of methylene chloride (1.0 L) of diethylamino malonate hydrochloride (47.0 g, 226 mmol) was cooled to 0 ° C. and pyridine (45 mL, 564 mmol) was added. The addition of pyridine dissolves the previously undissolved solid. Allyl chloroformate (20 mL, 188 mmol) was slowly added dropwise to maintain the temperature of the reaction at 5 ° C or lower. After the addition was complete, the reaction was stirred at 0 ° C. for 15 minutes. The reaction was washed with 1M hydrochloric acid (6 × 100 mL), dried over magnesium sulfate and concentrated in vacuo to afford the title compound as a white solid (46.78 g, 80%). The crude product was used without further purification. MS (CI) m / z 260.1 (M + l). [1135] H. 2- (5-Bromomethyl-isoxazol-3-yl) -pyrrolidine-1-carboxylic acid t-butyl ester [1136] [1137] The title compound was prepared using the 2- (hydroxyimino-methyl) -pyrrolidine-1-carbamic acid t-butyl ester of step 7I in the manner described in Examples 7H and 7I. [1138] Example 2 [1139] A. 2-allyloxycarbonylamino-3- (3- {1-[(4-nitro-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid [1140] [1141] A valence of 2-allyloxycarbonylamino-3- (3- {1-[(4-nitro-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid ethyl ester The digestion was carried out according to the same protocol as in Example 1A to afford the title compound. MS (CI) m / z 472.6 (M + 1), 471.7 (M-1). [1142] B. 2-allyloxycarbonylamino-3- (3- {1-[(4-nitro-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid ethyl ester [1143] [1144] A solution of dimethyl formamide (82 mL) of 4-nitrophenylacetic acid (1.61 g, 8.87 mmol) in dimethyl formamide (82 mL) was stirred with 4-hydroxybenzotriazole monohydrate (1.40 g, 10.4 mmol) for 10 minutes. I was. 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride (1.86 g, 9.72 mmol) is added and the mixture is added to all 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride Stir until dissolved. To this solution was added 2-allyloxycarbonylamino-3- (3-pyrrolidin-2-yl-isoxazol-5-yl) -propionic acid ethyl ester hydrochloride (3.16 g, 8.25 mmol) from Example 1C. The mixture was stirred for 30 minutes and then triethyl amine (1.26 mL, 9.04 mmol) was added. The reaction was stirred overnight at room temperature, then poured into water and extracted three times with ethyl acetate. The combined extracts were washed with saturated sodium bicarbonate solution, water (2 ×) and brine. The organic portion was dried over magnesium sulfate and concentrated. The resulting residue was chromatographed on a Biotage Flash 40S column eluting with ethyl acetate / hexanes (5: 1) to give the title compound as a yellow oil (674 mg, 15%). MS (CI) m / z 501.3 (M + l). In addition, the starting material 2-allyloxycarbonylamino-3- (3-pyrrolidin-2-yl-isoxazol-5-yl) -propionic acid ethyl ester was recovered (2.15 g, 75%). MS (CI) m / z 338.1 (M + l). [1145] Example 3 [1146] A. 2-allyloxycarbonylamino-3- [3- (1-{[4- (2,6-dichloro-benzoylamino) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazole -5-yl] -propionic acid [1147] [1148] 2-allyloxycarbonylamino-3- [3- (1-{[4- (2,6-dichloro-benzoylamino) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazole-5 Hydrolysis of -yl] -propionic acid ethyl ester was carried out according to the same protocol as in Example 1A to give the title compound (77 mg, 75%). MS (CI) m / z 616.7 (M + l), 612.5 (M-1). [1149] B. 2-allyloxycarbonylamino-3- [3- (1-{[4- (2,6-dichloro-benzoylamino) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazole -5-yl] -propionic acid ethyl ester [1150] [1151] 2-allyloxycarbonylamino-3- (3- {1-[(4-amino-phenyl) -acetyl-pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid ethyl ester (80 mg, 0.170 mmol) of dichloromethane (1 mL) solution was cooled to 0 ° C. and 2,6-dichlorobenzoylchloride (39 mg, 0.187 mmol) was added. The mixture was stirred for 15 minutes and then pyridine (28 μl, 0.34 mmol) was added. The reaction was slowly warmed to room temperature and stirred overnight. The reaction was diluted with ethyl acetate and washed with water, 1 M sodium hydroxide and brine. The organic portion was dried over magnesium sulfate and concentrated to give the title compound (84 mg, 78%). MS (CI) m / z 635.3 (M + l), 632.5 (M-1). [1152] C. 2-allyloxycarbonylamino-3- (3- {1-[(4-amino-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid ethyl ester [1153] [1154] 2-allyloxycarbonylamino-3- (3- {1-[(4-nitro-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid ethyl ester (2B ) (565 mg, 1.13 mmol) and iron (O) powder (384 mg, 6.98 mmol) in ethanol / water (5 mL, 1: 1) were heated to reflux. 1 M hydrochloric acid (0.29 mL, 0.29 mmol) was added dropwise and the reaction was heated to reflux for 45 minutes. It was then neutralized with 1 M sodium hydroxide and filtered through celite. The filtrate was diluted with ethyl acetate and washed with water and brine. The organic portion was dried over magnesium sulfate and concentrated in vacuo. The crude residue was chromatographed on a Biotage Flash 40S column eluting with ethyl acetate / hexanes (6: 1) to afford the title compound as a yellow oil (240 mg, 51%). MS (CI) m / z 471.0 (M + l). [1155] Example 4 [1156] A. 2-allyloxycarbonylamino-3- [3- (1-{[4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazole -5-yl] -propionic acid [1157] [1158] 2-allyloxycarbonylamino-3- [3- (1-{[4- (3-o-tolyl-ureido))-phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazole-5 Hydrolysis of -yl] -propionic acid ethyl ester was performed following the same protocol as in Example 1A to afford the title compound. MS (CI) m / z 576.0 (M + l), 573.9 (M-1). [1159] B. 2-allyloxycarbonylamino-3- [3- (1-{[4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazole -5-yl] -propionic acid ethyl ester [1160] [1161] The title compound was prepared in the manner described in Example 2B using [4- (3-o-tolyl-ureido) -phenyl] -acetic acid. MS (CI) m / z 604.0 (M + l). [1162] Example 5 [1163] A. 3- (3- {1-[(4-acetylamino-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -2-allyloxycarbonylamino-propionic acid [1164] [1165] 3- (3- {1-[(4-acetylamino-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -2-allyloxycarbonylamino-propionic acid ethyl ester Hydrolysis was carried out according to the same protocol as in Example 1A to afford the title compound. MS (CI) m / z 485.3 (M + 1), 483.0 (M-1). [1166] B. 3- (3- {1-[(4-acetylamino-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -2-allyloxycarbonylamino-propionate ethyl ester [1167] [1168] The title compound was prepared using acetyl chloride instead of 2,6-dichlorobenzoylchloride in the manner described in Example 3B. MS (CI) m / z 513.0 (M + l). [1169] Example 6 [1170] A. 2-t-butoxycarbonylamino-3- [3- (1-{[4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Isoxazol-5-yl] -propionic acid [1171] [1172] 2-t-butoxycarbonylamino-3- [3- (1-{[4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazole Hydrolysis of -5-yl] -propionic acid methyl ester was carried out according to the protocol of Example 1A to prepare the title compound. MS (CI) m / z 590.2 (M < -1 >), 492.2 (M-99). [1173] B. 2-t-Butoxycarbonylamino-3- [3- (1-{[4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Isoxazol-5-yl] -propionic acid methyl ester [1174] [1175] 1- (4- {2- [2- (hydroxyimino-methyl) -pyrrolidin-1-yl] -2-oxo-ethyl} -phenyl) -3-o-tolyl-urea (300 mg, 0.789 mmol) ), 2-t-butoxycarbonylamino-pent-4-inoic acid methyl ester (359 mg, 1.182 mmol, crude mixture) and solution of triethyl amine (12.9 μl) in dichloromethane (2 mL) for 5 minutes I was. Sodium hypochlorite solution (5.25%, 2 mL) was added. The reaction was stirred at rt overnight. The aqueous portion was extracted four times with dichloromethane. The combined organics were washed with brine, dried over magnesium sulfate and concentrated. The crude mixture was chromatographed on a Biotage Flash 40S column eluting with ethyl acetate / hexane 1: 5 to give the title compound (66 mg, 14%). MS (CI) m / z 604.5 (M-1), 505.9 (M-99). [1176] C. 2-t-butoxycarbonylamino-pent-4-inoic acid methyl ester [1177] [1178] Potassium carbonate (1.687 g, 12.2 mmol) is added to a solution of anhydrous methanol (91.5 mL) of 2-t-butoxycarbonylamino-pent-4-oxo-butyric acid benzyl ester (1.875 g, 6.10 mmol) and the reaction is carried out. Stir for 10 minutes. (1-diazo-2-oxo-propyl) -phosphonic acid dimethyl ester (1.407 g, 7.32 mmol) was added and the reaction was stirred at rt for 1 h. The reaction was poured into diethyl ether, washed four times with 5% sodium bicarbonate, dried over magnesium sulfate and concentrated (1.05 g, crude product mixture). The crude product was used directly in the next step. 1 H NMR (400 MHz, CDCl 3 ) δ 5.39-5.31 (m, 1H), 4.49-4.41 (m, 1H), 3.77 (s, 3H), 2.79-2.65 (m, 2H), 2.03 (s, 1H ), 1.59 and 1.44 (2 singlets, rotameter, 3H). [1179] D. 2-t-butoxycarbonylamino-4-oxo-butyric acid benzyl ester [1180] [1181] A dimethyl sulfoxide (10 mL) solution of 2-t-butoxycarbonylamino-4-hydroxy-butyric acid benzyl ester (13.58 g, 43.9 mmol) and triethyl amine (18.35 mL, 131.7 mmol) was cooled to 0 ° C. . Pyridine sulfur trioxide (21.0 g, 131.7 mmol) in dimethyl sulfoxide (80 mL) was added as a stable stream. The cooling bath was removed and the reaction stirred for 1.5 hours. The reaction was poured into 130 mL of ice water and extracted with diethyl ether (2 × 180 mL and 100 mL). The combined organics were washed with saturated sodium bicarbonate, water, brine and dried over magnesium sulfate. The solvent was removed in vacuo and the crude product was chromatographed on silica gel (900 mL) eluting with ethyl acetate / hexanes (1: 4) to afford the title compound as a clear colorless oil (9.20 g, 70%). MS (CI) m / z 208.0 (M-99). [1182] Example 7 [1183] A. 2-acetylamino-4- (3- {1- [2- (4-benzyloxy-phenyl) -acetylamino] -3-methyl-butyl} -isoxazol-5-yl) -propionic acid [1184] [1185] 2-acetylamino-4- (3- {1- [2- (4-benzyloxy-phenyl) -acetylamino] -3-methyl-butyl} -isoxazol-5-yl) -propionic acid ethyl ester (92 mg, 0.17 mmol) of a 1: 2 methanol / tetrahydrofuran (9 mL) solution was stirred for 3 hours in combination with 2M aqueous lithium hydroxide (3 mL) at room temperature. The reaction was acidified to pH 1 with 1N hydrochloric acid, and then the aqueous portion was extracted with ethyl acetate (2 x 50 mL). The combined organics were dried over sodium sulfate and concentrated to 2-acetylamino-4- (3- {1- [2- (4-benzyloxy-phenyl) -acetylamino] -3-methyl-butyl} -isoxazole -5-yl) -propionic acid was obtained as a white crystalline solid (83 mg, 95%). MS (CI) m / z 508.1 (M + l), 506.1 (M-1). [1186] B. 2-acetylamino-4- (3- {1- [2- (4-benzyloxy-phenyl) -acetylamino] -3-methyl-butyl} -isoxazol-5-yl) -propionic acid ethyl ester [1187] [1188] A solution of (4-benzyloxy-phenyl) -acetic acid (125 mg, 0.29 mmol, 1.00 equiv) and 1-hydroxybenzotriazole hydrate (48 mg, 0.36 mmol, 1.23 equiv) in dimethyl formamide (5 mL) was added at room temperature. Stir for minutes. 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide (64 mg, 0.33 mmol, 1.15 equiv) was added and the reaction was stirred for 15 minutes. 2-acetylamino-3- [3- (1-amino-3-methyl-butyl) -isoxazol-5-yl] -propionic acid ethyl ester hydrochloride (100 mg, 0.29 mmol, 1.00 equiv) was added and the reaction was carried out. Stir for 25 minutes. Triethylamine (43 μl, 0.31 mmol, 1.07 equiv) was added. The reaction was stirred at rt overnight, then diluted with ethyl acetate (30 mL) and extracted with 1N hydrochloric acid (2 × 30 mL), saturated sodium bicarbonate (2 × 30 mL) and brine (30 mL). The organic portion was dried over sodium sulfate and the solvent was removed in vacuo. The residue was chromatographed on 40S biotage column (ethyl acetate) to give the title compound as a clear colorless oil (94 mg, 61%). MS (CI) m / z 536.2 (M + l). [1189] C. 2-acetylamino-3- [3- (1-amino-3-methyl-butyl) -isoxazol-5-yl] -propionic acid ethyl ester hydrochloride [1190] [1191] 2-acetylamino-3- [3- (1-t-butoxycarbonylamino-3-methyl-butyl) -isoxazol-5-yl] -propionic acid ethyl ester (7F) (5.95 g, 14.5 mmol) Stir overnight in 4N hydrochloric acid in dioxane (25 mL) at room temperature. The product was concentrated and dried under high vacuum to give the title compound as a white solid (5.38 g, 100%). MS (CI) m / z 312.2 (M + 1 for free base). [1192] D. (4-benzyloxy-phenyl) -acetic acid [1193] [1194] A 1: 2 methanol / tetrahydrofuran (60 mL) solution of (4-benzyloxy-phenyl) -acetic acid methyl ester (1.35 g, 5.27 mmol) was combined with 2 M aqueous lithium hydroxide (20 mL) at room temperature and the reaction was overnight Stirred. The reaction was acidified to pH 1 with 1N hydrochloric acid and extracted with ethyl acetate (2 × 50 mL). The organic portion was dried over sodium sulfate and the solvent removed in vacuo to yield the title compound as a white crystalline solid (1.25 g, 98%). 1 H NMR (300 MHz, CDCl 3 ) δ 3.63 (s, 2H), 5.09 (s, 2H), 6.96-6.99 (d, 2H), 7.22-7.25 (d, 2H), 7.3-7.5 (m, 5H ). [1195] E. (4-benzyloxy-phenyl) -acetic acid methyl ester [1196] [1197] Cesium carbonate (5.35 g, 16.4 mmol, 3.00 equiv) was diluted with methyl 4-hydroxyphenyl acetate (1.00 g, 6.02 mmol, 1.10 equiv) and benzyl bromide (0.65 mL, 5.47 mmol, 1.00 equiv) at 0 ° C. 40 mL). The mixture was warmed to room temperature and stirred vigorously overnight. The reaction was extracted with 1N hydrochloric acid (2 × 100 mL) and brine (100 mL). The organic portion was dried over sodium sulfate and the solvent was removed in vacuo. The resulting oil solid was chromatographed on 40S biotage column (20% ethyl acetate / hexanes) to give the title ester as a clear colorless oil (1.35 g, 96%). 1 H NMR (400 MHz, CDCl 3 ) δ 3.56 (s, 2H), 3.67 (s, 3H), 5.04 (s, 2H), 6.91-6.94 (d, 2H), 7.17-7.19 (d, 2H), 7.3-7.4 (m, 5 H). [1198] F. 2-acetylamino-3- [3- (1-t-butoxycarbonylamino-3-methyl-butyl) -isoxazol-5-yl] -propionic acid ethyl ester [1199] [1200] 1 N sodium hydroxide (20.5 mL, 20.5 mmol, 1.10 equiv) was 2-acetylamino-2- [3- (1-t-butoxycarbonylamino-3-methyl-butyl) -isolate over 30 minutes at room temperature To a dioxane solution of sazol-5-ylmethyl] -malonic acid diethyl ester (8.99 g, 18.6 mmol, 1.0 equiv) was added and the reaction was stirred overnight. The reaction was diluted with ethyl acetate (200 mL) and acidified to pH 1-1.5 with 1 N hydrochloric acid. The organic portion was washed with brine (200 mL) and dried over sodium sulfate. Remove solvent under vacuum to afford 2-acetylamino-2- [3- (1-t-butoxycarbonylamino-3-methyl-butyl) -isoxazol-5-ylmethyl] -malonic acid monoethyl ester [MS (CI) m / z 356.3 (M-99)] and the decarboxylated title compound [MS (CI) m / z 412.3 (M + 1), 312.2 (M-99), 410.3 (M-1)] 8.58 g of a 1: 1 mixture (by 1 H NMR) was obtained. [1201] The mixture was refluxed in dioxane (150 mL) overnight and concentrated to give an orange oil which was chromatographed with a biotage column (40M, 50% ethyl acetate / hexanes) to give the title compound as a dark orange solid (6.72). g, 88%). MS (CI) m / z 412.3 (M + 1), 312.2 (M-99). [1202] G. 2-acetylamino-2- [3- (1-t-butoxycarbonylamino-3-methyl-butyl) -isoxazol-5-ylmethyl] -malonic acid diethyl ester [1203] [1204] Cesium carbonate (18.28 g, 56.1 mmol, 3.0 equiv) was purified at 0 ° C. [1- (5-bromomethyl-isoxazol-3-yl) -3-methyl-butyl] -carbamic acid t-butyl ester , 18.7 mmol, 1.00 equiv) and diethylacetamidomalonate (4.86 g, 22.4 mmol, 1.20 equiv) were added to a solution of dimethyl formamide (300 mL). The mixture was stirred at rt for 5 h. The reaction was poured into diethyl ether (200 mL) and extracted with water (5 x 200 mL) and brine (200 mL). The organic portion was dried over sodium sulfate and the solvent was removed in vacuo to give the title compound as sticky oil (8.99 g, 99.4%). MS (CI) m / z 484.0 (M + l), 384.1 (M-99). [1205] H. [1- (5-Bromomethyl-isoxazol-3-yl) -3-methyl-butyl] -carbamic acid t-butyl ester [1206] [1207] N-chlorosuccinimide (5.80 g, 43.4 mmol, 1.00 equiv), [1- (hydroxyimino-methyl) -3-methyl-butyl] -carbamic acid t-butyl ester (10.00 g, 43.4 mmol, 1.00 equiv ) And pyridine (0.70 mL) were stirred in chloroform (70 mL) at room temperature for 1 hour. Propargyl bromide (4.83 mL, 54.3 mmol, 1.25 equiv) was added and the reaction heated to 45 ° C. Triethylamine (6.35 mL, 45.6 mmol, 1.05 equiv) was added dropwise at 45 ° C. over 20 minutes. The reaction was stirred for an additional hour, then diluted with water (200 mL) and extracted with dichloromethane (2 × 200 mL). The combined organics were washed with saturated sodium bicarbonate (2 x 200 mL) and brine (200 mL). The organic portion was dried over sodium sulfate. The solvent was evaporated to give a brown residue which was chromatographed by flash chromatography on silica gel to give the title compound as a white solid (6.48 g, 43%). MS (CI) m / z 247.0 (M-99). [1208] I. 1- (hydroxyimino-methyl) -3-methyl-butyl] -carbamic acid t-butyl ester [1209] [1210] MeOH (20 mL) of (1-formyl-3-methyl-butyl) -carbamic acid t-butyl ester (2.13 g), hydroxylamine hydrochloride (0.71 g, 10.2 mmol) and NaOAc (2 g, 24.4 mmol) and The mixture in water (20 mL) was stirred vigorously. After 24 hours, the mixture was diluted with water (60 mL) and extracted with EtOAc (50 mL × 3). The combined organics were washed with water and brine, dried over MgSO 4 , filtered and concentrated under reduced pressure. Purification by flash 40 chromatography using a silica gel column eluting with 15-25% EtOAc / hexanes afforded 1.5 g of the title compound as a white solid. MP 156-157 ° C. [1211] Example 8 [1212] A. 2-allyloxycarbonylamino-3- [3- (1-benzoyl-pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid [1213] [1214] Hydrolysis of 8B was performed following the protocol of Example 1A to afford the title compound. MS (CI) m / z 414.2 (M + l), 412.2 (M-1). [1215] B. 2-allyloxycarbonylamino-3- [3- (1-benzoyl-pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid ethyl ester [1216] [1217] Benzoyl chloride (21 μl, 0.18 mmol, 1.0 equiv) was 2-allyloxycarbonylamino-3- (3-pyrrolidin-2-yl-isoxazol-5-yl) -propionic acid ethyl ester hydrochloride at 0 ° C. (1C) (74 mg, 0.20 mmol, 1.1 equiv) was added in 1 part to a solution in pyridine (29 μl, 0.36 mmol, 2.0 equiv) and dichloromethane (2 mL). The reaction was stirred at rt for 4 h and then diluted with ethyl acetate (30 mL). The reaction was extracted with 1N hydrochloric acid (30 mL) and brine (30 mL). The organic portion was dried over sodium sulfate and concentrated in vacuo to afford the title compound (66 mg, 84%). MS (CI) m / z 442.3 (M + l). [1218] Example 9 [1219] A. 2-allyloxycarbonylamino-3- {3- [1- (biphenyl-4-carbonyl) -pyrrolidin-2-yl] -isoxazol-5-yl} -propionic acid [1220] [1221] Hydrolysis of 9B was performed following the protocol of Example 1A to afford the title compound. MS (CI) m / z 490.0 (M + l), 487.8 (M-1). [1222] B. 2-allyloxycarbonylamino-3- {3- [1- (biphenyl-4-carbonyl) -pyrrolidin-2-yl] -isoxazol-5-yl} -propionic acid ethyl ester [1223] [1224] Prepared using the method as described in Example 8B. MS (CI) m / z 518.0 (M + l). [1225] Example 10 [1226] A. 2-acetylamino-3- (3- {3-methyl-1- [2- (4-naphthalen-2-yl-phenyl) -acetylamino] -butyl} -isoxazol-5-yl) -propionic acid [1227] [1228] Hydrolysis of 10B was performed according to the protocol of Example 1A to afford the title compound. MS (CI) m / z 528.0 (M + l), 525.8 (M-1). [1229] B. 2-acetylamino-3- (3- {3-methyl-1- [2- (4-naphthalen-2-yl-phenyl) -acetylamino] -butyl} -isoxazol-5-yl) -propionic acid [1230] [1231] Prepared from (4-naphthalen-2-yl-phenyl) -acetic acid in the manner described in Example 7B. [1232] C. (4-naphthalen-2-yl-phenyl) -acetic acid [1233] [1234] 2 M lithium hydroxide (3.0 mL) was added to a 2: 1 tetrahydrofuran: methanol (9.0 mL) solution of (4-naphthalen-2-yl-phenyl) -acetic acid methyl ester (270 mg, 0.977 mmol). The resulting mixture was stirred at rt for 1 h. The reaction was acidified to pH 1 with 1 M hydrochloric acid and extracted twice with ethyl acetate. The combined organics were washed with brine, dried over magnesium sulfate and concentrated in vacuo to afford the title compound as a white solid (233 mg, 91%). 1 H NMR (400 MHz, CDCl 3 ) δ 8.01-7.39 (m, 11H), 3.72 (s, 2H). [1235] D. (4-naphthalen-2-yl-phenyl) -acetic acid methyl ester [1236] [1237] Tetrakis triphenylphosphine palladium (65 mg, 7.4 mol%) (4-trifluoromethanesulfonyloxy-phenyl) -acetic acid methyl ester (447 mg, 1.5 mmol), 2-naphthalene boronic acid (286 mg, 1.67 mmol) And cesium fluoride (505 mg, 3.33 mmol) in a dimethoxy ethane (5.4 mL) solution. The reaction was washed down with nitrogen and heated to 100 ° C. in an oil bath with stirring for 3 hours. The reaction was then diluted with ethyl acetate and extracted with water, 1 M sodium hydroxide, water and brine. The organic portion was dried over magnesium sulfate and concentrated in vacuo. The resulting residue was chromatographed on a Biotage Flash 40S column eluting with 5% ethyl acetate in hexanes to give the title compound as a clear oil (273 mg, 66%). 1 H NMR (400 MHz, CDCl 3 ) δ 8.01-7.38 (m, 11H), 3.72 (s, 3H), 3.69 (2H). [1238] E. (4-Trifluoromethanesulfonyloxy-phenyl) -acetic acid methyl ester [1239] [1240] Trifluoromethane sulfone anhydride (32.2 mmol) was added dropwise to a 40 ° C. pyridine (70 mL) solution of (4-hydroxy-phenyl) -acetic acid methyl ester (5.35 g, 32.2 mmol) over 5 minutes. The reaction was stirred at −40 ° C. for 10 minutes and then at 0 ° C. for 2 hours. The reaction was diluted with diethyl ether and washed with water and 2N hydrochloric acid. The organic portion was dried over magnesium sulfate and concentrated in vacuo. The crude residue was chromatographed on a Biotage Flash 40M column, eluting with ethyl acetate / hexanes (1: 4) to give 9.27 g (97%) as a clear colorless oil that crystallized off the title compound. 1 H NMR (400 MHz, CDCl 3 ) δ 7.37-7.34 (m, 2H), 7.24-7.21 (m, 2H), 3.70 (3H), 3.64 (2H). [1241] Example 11 [1242] A. 2,2-Dimethyl-3- [3- (3-methyl-1- {2- [4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -butyl) -isoxazole- 5-yl] -propionic acid [1243] [1244] Hydrolysis of 11B was carried out according to the protocol of Example 1A to afford the title compound. MS (CI) m / z 521.2 (M + 1), 519.1 (M-1). [1245] B. 2,2-Dimethyl-3- [3- (3-methyl-1- {2- [4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -butyl) -isoxazole- 5-yl] -propionic acid methyl ester [1246] [1247] 3- [3- (1-t-butoxycarbonylamino-3-methyl-butyl) -isoxazol-5-yl] -2,2-dimethyl-propionic acid in two steps according to the procedure of Examples 1C and 2B Prepared from methyl ester. MS (CI) m / z 535.1 (M + l), 535.1 (M-1). [1248] C. 3- [3- (1-t-butoxycarbonylamino-3-methyl-butyl) -isoxazol-5-yl] -2,2-dimethyl-propionic acid methyl ester [1249] [1250] From [1- (hydroxyimino-methyl) -3-methyl-butyl] -carbamic acid t-butyl ester (7I) and 2,2-dimethyl-pent-4-inoic acid methyl ester according to the procedure of Example 6A Prepared. MS (CI) m / z 313.2 (M-tBu), 269.3 (M-99). [1251] Example 12 [1252] A. 3- [3- (3-Methyl-1- {2- [4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -butyl) -isoxazol-5-yl] -2 -Phenyl-propionic acid [1253] [1254] Hydrolysis of 12B was performed according to the protocol of Example 1A to afford the title compound. [1255] B. 3- [3- (3-Methyl-1- [2- {4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -butyl) -isoxazol-5-yl] -2 -Phenyl-propionic acid methyl ester [1256] [1257] The title compound was prepared from 3- [3- (1-t-butoxycarbonylamino-3-methyl-butyl) -isoxazol-5-yl] -2-phenyl-propionic acid methyl ester in the manner described in Example 11B. Prepared. [1258] C. 3- [3- (1-t-butoxycarbonylamino-3-methyl-butyl) -isoxazol-5-yl] -2-phenyl-propionic acid methyl ester [1259] [1260] The title compound was prepared from 2-phenyl-pent-4-inoic acid methyl ester in the manner described in Example 6A. [1261] D. 2-phenyl-pent-4-inoic acid methyl ester [1262] [1263] Diisopropyl ethyl amine (5.9 mL, 42 mmol) was dissolved in tetrahydrofuran (30 mL). 2.5 M butyllithium (16.8 mL, 42 mmol) in hexane was added slowly. A solution of phenyl acetic acid (2.72 g, 20 mmol) in tetrahydrofuran (20 mL) was added slowly over 20 minutes via a dropping funnel. The reaction was stirred for 25 minutes. Propargyl bromide was added as an 80 wt% solution in toluene (2.3 mL, 21.0 mmol). The reaction was stirred for 1.5 hours and 4N hydrochloric acid (15 mL) was added. The mixture was diluted with ethyl acetate (50 mL). The organics were concentrated in vacuo. The residue was dissolved in diethyl ether and extracted with water (3 ×) and 1N hydrochloric acid (3 ×). The organic portion was dried over magnesium sulfate and the solvent was removed in vacuo. The resulting yellow solid (1.7 g) was dissolved in methanol (50 mL) and cooled to 0 ° C. Acetylchloride (2 mL) was added and the reaction was allowed to warm to room temperature. After the reaction was stirred for 18 hours, the solvent was removed in vacuo. The residue was dissolved in diethyl ether. The solution was extracted with saturated sodium bicarbonate, water and brine. The organic portion was dried over magnesium sulfate and the solvent was removed in vacuo. The residue was chromatographed on silica gel with 10% ethyl acetate in hexanes to give the title compound as an oil (0.58 g, 15%). [1264] Example 13 [1265] A. 2-acetylamino-3- [3- (1-{[4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazole-5- General] -propionic acid [1266] [1267] Hydrolysis of 13B was carried out according to the protocol of Example 1A to afford the title compound. MS (CI) m / z 534.2 (M + l), 532.4 (M-1). [1268] B. 2-acetylamino-3- [3- (1-{[4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazole-5- General] -propionic acid ethyl ester [1269] [1270] The title compound was prepared as described in Example 11B 2- [5- (2-acetylamino-2-methoxycarbonyl-ethyl) -isoxazol-3-yl] -pyrrolidine-1-carboxylic acid t-butyl Prepared from esters. MS (CI) m / z 562.1 (M + 1). [1271] C. 2- [5- (2-acetylamino-2-methoxycarbonyl-ethyl) -isoxazol-3-yl] -pyrrolidine-1-carboxylic acid t-butyl ester [1272] [1273] The title compound was prepared from 2- (hydroxyimino-methyl) -pyrrolidine-1-carbamic acid t-butyl ester and 2-acetylamino-pent-4-inoic acid methyl ester as described in Example 6B. . MS (CI) m / z 296.0 (M-99). [1274] Example 14 [1275] A. 2- (2,6-Dichloro-benzoylamino) -3- [3- (1-{[4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidine-2- Yl) -isoxazol-5-yl] -propionic acid [1276] [1277] Hydrolysis of 14B was performed following the protocol of Example 1A to afford the title compound. MS (CI) m / z 663.8 (M + l). [1278] B. 2- (2,6-Dichloro-benzoylamino) -3- [3- (1-{[4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidine-2- Yl) -isoxazol-5-yl] -propionic acid ethyl ester [1279] [1280] The title compound was prepared in the same manner as described in 11B in 2- {5- [2- (2,5-dichloro-benzoylamino) -2-ethoxycarbonyl-ethyl] -isoxazol-3-yl} -pyrroli Prepared from dean-1-carboxylic acid t-butyl ester. MS (CI) m / z 691.8 (M + 1), 689.7 (M-1). [1281] C. 2- {5- [2- (2,6-Dichloro-benzoylamino) -2-ethoxycarbonyl-ethyl] -isoxazol-3-yl} -pyrrolidine-1-carboxylic acid t-butyl ester [1282] [1283] The title compound was prepared in the manner described in Example 3B 2- [5- (2-amino-2-ethoxycarbonyl-ethyl) -isoxazol-3-yl] -pyrrolidine-1-carboxylic acid t-butyl ester Prepared from hydrochloride and 2,6-dichlorobenzoylchloride. MS (CI) m / z 525.9 (M + 1), 425.9 (M-99). [1284] D. 2- [5- (2-Amino-2-ethoxycarbonyl-ethyl) -isoxazol-3-yl] -pyrrolidine-1-carboxylic acid t-butyl ester hydrochloride [1285] [1286] 2- {5- [2- (Benzhydrylidene-amino) -2-ethoxycarbonyl-ethyl] -isoxazol-3-yl} -pyrrolidine-1-carboxylic acid t-butyl ester (700 mg, 1.35 mmol) was stirred in a mixture of ethyl acetate (20 mL) and 1N hydrochloric acid (100 mL) for 3 hours. The reaction was neutralized by the addition of saturated sodium bicarbonate. The aqueous portion was extracted with diethyl ether. The combined organics were dried over magnesium sulfate and the solvent was removed in vacuo. The resulting oil (200 mg) was used directly in Example 14C. [1287] E. 2- {5- [2- (Benzhydrylidene-amino) -2-ethoxycarbonyl-ethyl] -isoxazol-3-yl} -pyrrolidine-1-carboxylic acid t-butyl ester [1288] [1289] 2- (5-Bromomethyl-isoxazol-3-yl) -pyrrolidine-1-carboxylic acid t-butyl ester (1.0 g, 3 mmol) and N- (diphenylmethylene) glycine glycine ethyl ester (1.0 g, 3.74 mmol) was dissolved in toluene (10 mL). 18 M aqueous potassium hydroxide (0.25 mL, 4.5 mmol) and tetrabutylammonium bromide (97 mg, 0.30 mmol) were added. The reaction was stirred at rt for 1 h, then 1N hydrochloric acid (4.5 mL) was added. The organic phase was extracted with 1N hydrochloric acid, saturated sodium bicarbonate and brine. The organic portion was dried over magnesium sulfate and the solvent was removed in vacuo. The residue was chromatographed on a Biotage 40S column using 15% ethyl acetate in hexanes to give the title compound (700 mg, 45%). MS (CI) m / z 518.0 (M + l). [1290] Example 15 [1291] A. 2-allyloxycarbonylamino-3- {3- [1- (toluene-4-sulfonyl) -pyrrolidin-2-yl] -isoxazol-5-yl} -propionic acid [1292] [1293] Hydrolysis of 15B was performed according to the protocol of Example 1A to afford the title compound. MS (CI) m / z 464.0 (M + 1), 461.9 (M-1). [1294] B. 2-allyloxycarbonylamino-3- {3- [1- (toluene-4-sulfonyl) -pyrrolidin-2-yl] -isoxazol-5-yl} -propionic acid ethyl ester [1295] [1296] The title compound was prepared according to the method described in Example 1B. MS (CI) m / z 492.0 (M + l). [1297] Example 16 [1298] A. 2-allyloxycarbonylamino-3- [3- (1-{[4- (2,6-dimethoxy-benzoylamino) -phenyl] -acetyl} -pyrrolidin-2-yl) -isolate Sazol-5-yl] -propionic acid [1299] [1300] Hydrolysis of 16B was performed according to the protocol of Example 1A to afford the title compound. MS (CI) m / z 606.7 (M + l), 605.1 (M-1). [1301] B. 2-allyloxycarbonylamino-3- [3- (1-{[4- (2,6-dimethoxy-benzoylamino) -phenyl] -acetyl} -pyrrolidin-2-yl) -isobutyrate Sazol-5-yl] -propionic acid ethyl ester [1302] [1303] The title compound was prepared using 2,6-dimethoxybenzoylchloride instead of 2,6-dichlorobenzoylchloride according to the procedure described in Example 3B. MS (CI) m / z 635.3 (M + l), 632.5 (M-1). [1304] Example 17 [1305] A. 2-allyloxycarbonylamino-3- {3- [1- (3,4-dimethoxy-benzenesulfonyl) -pyrrolidin-2-yl] -isoxazol-5-yl} -propionic acid [1306] [1307] Hydrolysis of 17B was carried out according to the protocol of Example 1A to afford the title compound. MS (CI) m / z 507.6 (M-1). [1308] B. 2-allyloxycarbonylamino-3- {3- [1- (3,4-dimethoxy-benzenesulfonyl) -pyrrolidin-2-yl] -isoxazol-5-yl} -ethyl propionate ester [1309] [1310] The title compound was prepared using 3,4-dimethoxybenzenesulfonylchloride according to the method described in Example 1B. MS (CI) m / z 537.8 (M + l). [1311] Example 18 [1312] A. 2-allyloxycarbonylamino-3- [3- (1-cyclopropanecarbonyl-pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid [1313] [1314] Hydrolysis of 18B was performed according to the protocol of Example 1A to afford the title compound. MS (CI) m / z 378.2 (M + l), 376.2 (M-1). [1315] B. 2-allyloxycarbonylamino-3- [3- (1-cyclopropanecarbonyl-pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid ethyl ester [1316] [1317] The title compound was prepared using a suitable reagent according to the method described in Example 3B. MS (CI) m / z 406.1 (M + l). [1318] Example 19 [1319] A. 2-acetylamino-3- [3- (3-methyl-1- {2- [4- (2-methyl-benzyloxy) -phenyl] -acetylamino} -butyl) -isoxazol-5-yl ] -Propionic acid [1320] [1321] Hydrolysis of 19B was performed following the protocol of Example 1A to prepare the title compound. MS (CI) m / z 508.1 (M + l), 506.1 (M-1). [1322] B. 2-acetylamino-3- [3- (3-methyl-1- {2- [4- (2-methyl-benzyloxy) -phenyl] -acetylamino} -butyl) -isoxazol-5-yl ] -Propionic acid ethyl ester [1323] [1324] The title compound was prepared using [4- (2-methyl-benzyloxy) -phenyl] -acetic acid according to the method described in Example 7B. MS (CI) m / z 550.2 (M + l). [1325] C. [4- (2-Methyl-benzyloxy) -phenyl] -acetic acid [1326] [1327] The title compound was prepared according to the method described in Example 7D. 1 H NMR (300 MHz, CDCl 3 ) δ 2.40 (s, 3H), 3.65 (s, 2H), 5.05 (s, 2H), 6.98-7.01 (d, 2H), 7.02-7.30 (m, 5H), 7.42-7.44 (d, 1 H). [1328] D. [4- (2-Methyl-benzyloxy) -phenyl] -acetic acid methyl ester [1329] [1330] The title compound was prepared according to the method described in Example 7E. 1 H NMR (400 MHz, CDCl 3 ) δ2.35 (s, 3H), 3.65 (s, 2H), 3.67 (s, 3H), 5.00 (s, 2H), 6.92-6.94 (d, 2H), 7.18- 7.26 (m, 5 H), 7.37-7.39 (d, 1 H). [1331] Example 20 [1332] A. 2-acetylamino-3- (3- {1- [2- (4'-ethyl-biphenyl-4-yl) -acetylamino] -3-methyl-butyl} -isoxazol-5-yl ) -Propionic acid [1333] [1334] Hydrolysis of 20B was performed according to the protocol of Example 1A to afford the title compound. MS (CI) m / z 506.1 (M + l), 504.0 (M-1). [1335] B. 2-acetylamino-3- (3- {1- [2- (4'-ethyl-biphenyl-4-yl) -acetylamino] -3-methyl-butyl} -isoxazol-5-yl ) -Propionic acid ethyl ester [1336] [1337] The title compound was prepared using (4'-ethyl-biphenyl-4-yl) -acetic acid according to the method described in Example 7B. MS (CI) m / z 534.2 (M + l). [1338] C. (4'-Ethyl-biphenyl-4-yl) -acetic acid [1339] [1340] The title compound was prepared according to the method described in Example 10B. MS (CI) m / z 239.0 (M-1). [1341] D. (4'-Ethyl-biphenyl-4-yl) -acetic acid methyl ester [1342] [1343] The title compound was prepared according to the method described in Example 10C. 1 H NMR (400 MHz, CDCl 3 ) δ7.63 (d, J = 8.1 Hz, 2H), 7.60 (d, J = 8.1 Hz, 2H), 7.43 (d, J = 8.1 Hz, 2H), 7.36 (d , J = 8.1 Hz, 2H), 3.79 (s, 3H), 3.75 (s, 3H), 2.78 (q, J = 7.5 Hz, 2H), 1.37 (t, J = 7.5 Hz, 3H). [1344] Example 21 [1345] A. 2-acetylamino-3- (3- {1-[(4-benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid [1346] [1347] The title compound was purified using the method of Example 1D 2-acetylamino-2- (3- {1-[(4-benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazole-5 Prepared from -ylmethyl) -malonic acid diethyl ester. MS (CI) m / z 492.2 (M + l), 490.3 (M-1). [1348] B. 2-acetylamino-2- (3- {1-[(4-benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-ylmethyl) -malonic acid diethyl ester [1349] [1350] MS (CI) m / z 602.0 (M + l). [1351] Example 22 [1352] A. 2-acetylamino-3- [3- (1-{[4- (4-chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] Propionic acid [1353] [1354] The title compound was prepared from 22B following the method described in Example 21A. MS (CI) m / z 526.2 (M + l), 524.2 (M-1). [1355] B. 2-acetylamino-3- [3- (1-{[4- (4-chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-ylmethyl ) -Malonic acid diethyl ester [1356] [1357] The title compound was prepared according to the method described in Example 21B using [4- (4-chloro-benzyloxy) -phenyl] -acetic acid. MS (CI) m / z 626.0 (M + l). [1358] C. [4- (4-Chloro-benzyloxy) -phenyl] -acetic acid [1359] [1360] The title compound was prepared according to the method described in Example 7D. 1 H NMR (400 MHz, dimethyl sulfoxide) δ 3.44 (s, 2H), 5.05 (s, 2H), 6.88-6.92 (m, 2H), 7.11-7.14 (m, 2H), 7.42 (s, 4H) , 12.20 (s, 1 H). 13 C NMR (100 MHz, dimethyl sulfoxide) δ 68.9, 115.2, 128.1, 129.1, 130.1 (two overlapping peaks), 131.1, 133.0, 136.9, 157.5, 173.6. [1361] D. [4- (4-Chloro-benzyloxy) -phenyl] -acetic acid methyl ester [1362] [1363] The title compound was prepared according to the method described in Example 7E. 1 HNMR (400 MHz, CDCl 3 ) δ 3.55 (s, 2H), 3.67 (s, 3H), 5.00 (s, 2H), 6.88-6.90 (d, 2H), 7.17-7.19 (d, 2H), 7.34 (s, 4H). [1364] Example 23 [1365] A. 2-acetylamino-3- [3- (1-{[4- (3-phenyl-allyl) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl]- Propionic acid [1366] [1367] The title compound was prepared from 23B following the method described in Example 22A. MS (CI) m / z 502.2 (M + l), 500.2 (M-1). [1368] B. 2-acetylamino-3- [3- (1-{[4- (3-phenyl-allyl) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-ylmethyl) Malonic acid diethyl ester [1369] [1370] The title compound was prepared from [4- (3-phenyl-allyl) -phenyl] -acetic acid according to the method described in Example 22B. MS (CI) m / z 602.0 (M + l). [1371] C. [4- (3-phenyl-allyl) -phenyl] -acetic acid [1372] [1373] The title compound was prepared from [4- (3-phenyl-allyl) -phenyl] -acetic acid according to the method described in Example 10B. 1 H NMR (400 MHz, CDCl 3 ) δ 3.51 (d, 2H, J = 7 Hz), 3.62 (s, 2H), 6.28-6.46 (m, 2H), 7.18-7.37 (m, 9H). [1374] D. [4- (3-phenyl-allyl) -phenyl] -acetic acid [1375] [1376] (4-Trifluoromethanesulfonyloxy-phenyl) -acetic acid methyl ester (500 mg, 1.68 mmol, 1.00 equiv), palladium (II) chloride (15 mg, 5 mol%), bis-diphenylphosphinoethane (50 mg, 5 mol %), Bis (pinacolato) diboron (469 mg, 1.85 mmol, 1.10 equiv) and potassium acetate (495 mg, 5.04 mmol, 3.00 equiv) were heated in dimethyl formamide (10 mL) at 80 ° C. for 3 hours. The black reaction mixture was cooled to room temperature. Palladium (II) chloride (15 mg, 5 mol%), bis-diphenylphosphinoethane (50 mg, 5 mol%), cinnamil bromide (660 mg, 3.35 mmol, 2.00 equiv), sodium carbonate (890 mg, 8.40 mmol, 5.00 equiv) and Water (4 mL) was added. The reaction mixture was heated to 80 ° C overnight. The reaction was cooled to rt and diluted with ethyl acetate (50 mL). The mixture was extracted with saturated sodium bicarbonate (2 × 50 mL), water (2 × 50 mL) and brine (50 mL). The organic portion was dried over sodium sulfate. The solvent was evaporated to give a black oil residue which was chromatographed on biotease (5% ethyl acetate / hexane) to give a 9: 1 mixture of the title compound and acetic acid 3-phenyl-allyl ester (200 mg, 45%). 1 H NMR (400 MHz, CDCl 3 ) δ 3.52 (dd, 2H, J = 7, 1.2 Hz), 3.60 (s, 2H), 3.68 (s, 3H), 6.24-6.38 (m, 1H), 6.43- 6.47 (d, 1 H), 7.1-7.4 (m, 9 H). This material was used in Example 23C without further purification. [1377] Example 24 [1378] A. 2- (3-Methyl-1- {2- [4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -butyl) -1H-benzoimidazole-4-carboxylic acid [1379] [1380] The title compound was prepared from 24B following the method described in Example 1A. MS (CI) m / z 514.1 (M + 1), 512.2 (M-1). [1381] B. 2- (3-Methyl-1- {2- [4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -butyl) -1 H-benzoimidazole-4-carboxylic acid methyl ester [1382] [1383] The title compound was prepared from 24C according to the method described in Example 2B. MS (CI) m / z 528.0 (M + l), 526.2 (M-1). [1384] C. 2- (1-Amino-3-methyl-butyl) -1 H-benzoimidazole-5-carboxylic acid methyl ester hydrochloride [1385] [1386] A solution of 4-amino-3- (2-t-butoxycarbonylamino-4-methyl-pentanoylamino) -benzoic acid methyl ester (690 mg, 1.82 mmol) in acetic acid (9 mL) was stirred at 70 ° C. for 1.5 hours. Heated. Acetic acid was removed under vacuum and the crude mixture was dissolved in 4M hydrochloric acid in dioxane (9 mL) and stirred at room temperature for 30 minutes. The reaction was concentrated in vacuo to afford the title compound. MS (CI) m / z 262.0 (M + 1), 260.1 (M-1). [1387] E. 4-Amino-3- (2-t-butoxycarbonylamino-4-methyl-pentanoylamino) -benzoic acid methyl ester [1388] [1389] Hydroxybenzotriazole monohydrate (760 mg. 5.62 mmol) and 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride (973 mg, 5.07 mmol) were converted into Nt-butoxycarbonyl-L-leucine ( 1.06 g, 4.57 mmol) in dimethyl formamide (30 mL) solution. The mixture was stirred until all 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride was dissolved. Methyl 3,4-diaminobenzoate (759 mg, 4.57 mmol) and triethyl amine (0.68 mL, 4.89 mmol) in dimethyl formamide (10 mL) were added sequentially. The reaction was stirred at rt overnight and poured into water. The mixture was extracted three times with ethyl acetate. The organic portion was extracted with a saturated solution of sodium bicarbonate, water (2 ×) and brine. The organic portion was dried over magnesium sulfate and the solvent was removed in vacuo. The resulting residue was chromatographed on a Biotage Flash 40S column eluting with ethyl acetate / hexanes (2: 3) to give the title compound (690 mg, 40%). MS (CI) m / z 380.0 (M + l), 378.2 (M-1). [1390] Example 25 [1391] A. 2- (2,6-Dichloro-benzoylamino) -3- [3- (1- [2- [3-methoxy-4- (3-o-tolyl-ureaido) -phenyl] -acetylamino } -3-methyl-butyl) -isoxazol-5-yl] -propionic acid [1392] [1393] A mixture of 25B (56 mg, 0.13 mmol) in t-butanol (1 mL) and 1N sodium hydroxide (0.27 mL) was stirred at reflux. After 30 minutes, the mixture was concentrated under reduced pressure and the resulting residue was dissolved in water and washed with ethyl acetate. The aqueous layer was acidified to pH 1 with 1N HCl and extracted with ethyl acetate. The combined organic layers were washed with water and brine, dried over sodium sulfate and concentrated under reduced pressure to yield an off-white solid. MP 102-4 ° C .; MS m / z 710.3 and 713.3 (M + 1). [1394] B. 2- (2,6-Dichloro-benzoylamino) -3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureaido) -phenyl] -acetylamino } -3-methyl-butyl) -isoxazol-5-yl] -propionic acid methyl ester [1395] [1396] The title compound was purified by 3-methoxy-4- (3-o-tolyl-ureido) -phenylacetic acid and 3- [3- (1-amino-3-methyl-butyl) -isoxazol-5-yl] -2 Prepared in the manner described in Example 2B using-(2,6-dichloro-benzoylamino) -propionic acid methyl ester hydrochloride. 51% yield; White solid. MS m / z 724.2 and 726.2 (M + l). [1397] C. 3- [3- (1-Amino-3-methyl-butyl) -isoxazol-5-yl] -2- (2,6-dichloro-benzoylamino) -propionic acid methyl ester hydrochloride [1398] [1399] The title compound was prepared from 25D in the same manner as in Example 1C. MS (m / z) 428.3 and 430.3 (M + l). [1400] D. 3- [3- (1-T-butoxycarbonylamino-3-methyl-butyl) -isoxazol-5-yl] -2- (2,6-dichloro-benzoylamino) -propionic acid methyl ester [1401] [1402] The title compound was prepared from 25E and 7I in the same manner as in Example 7H. MS (m / z) 526.2 and 528.0 (M-1). [1403] E. 2- (2,6-Dichloro-benzoylamino) -pent-4-inoic acid methyl ester [1404] [1405] The title compound was prepared from 2-amino-pent-4-inoic acid methyl ester and 2,5-dichlorobenzoyl chloride in the same manner as in Example 3B. MS (m / z) 300.2 and 302.2 (M + l). [1406] Example 26 [1407] A. 2- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -isoxazole-5 -Ylmethyl] -4-methyl-pentanoic acid [1408] [1409] The title compound was prepared in the same manner as Steps A through D of Example 25 using the 4-methyl-2-propargyl pentanic acid methyl ester of step D. MS (m / z) 577.3 (M-1). [1410] Example 27 [1411] A. 2-acetylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Isoxazol-5-yl] -propionic acid [1412] [1413] The title compound was prepared in the same manner as in Examples 7A and B, using 25B 3-methoxy-4- (3-o-tolyl-ureido) -phenylacetic acid. White solid; MP 123-5 ° C .; MS (m / z) 578.1 (M-1). [1414] Example 28 [1415] A. 2-Acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -amino) -methyl] -phenyl} -propionic acid [1416] [1417] The title compound was prepared in the same manner as Steps A and B of Example 25 using 28B of step 25B. MS (m / z) 633 (M + l). [1418] B. 2-acetylamino-2-[(3-aminomethyl-phenyl) -methyl] -malonic acid diethyl ester [1419] [1420] A mixture of 28C (1.15 g, 3.5 mmol), 10% Pd on carbon (0.15 g) and concentrated HCl (0.3 mL) in ethanol (50 mL) was placed in a Parr shaker for 6 hours under 45 psi hydrogen. The mixture was filtered through celite and concentrated under reduced pressure to give 1.2 g of the title compound as a white solid. MS (m / z) 337.3 (M + l). [1421] C. 2-acetylamino-2-[(3-cyanophenyl) -methyl] -malonic acid diethyl ester [1422] [1423] The title compound was prepared from α-bromo-meth-tolunitrile in the same manner as in Example 7G. MS (m / z) 333 (M + l). [1424] Example 29 [1425] Binding of biotinylated CS-1 to Isolated VLA-4 [1426] The VLA-4 / bCS-1 receptor ligand binding assays described herein test the ability of a compound to specifically inhibit VLA-4 dependent binding. [1427] A. Preparation of VLA-4 Cladding Plate [1428] The VLA-4 cladding was prepared the day before the assay was performed. VLA-4 expressing species are described in Macarem et al ., J. Biol. Chem. , 269, 4005-4011 (1994)], were isolated from Jurkat cells and diluted to a final concentration of 0.4 mg / ml in 50 mM NaHCO 3 (pH 8.8). A 100 ml aliquot of the original seed solution was then added to each well of a 96 well microfluorine "B" U-shaped bottom plate (Dynatech No. 0010107205) and incubated overnight at 4 ° C. The coating solution was removed by aspiration and the wells were quenched (200 ml / well, 37 ° C.) for 0.5 h using PBS and 1 mM MnCl containing 1% fat free dry milk. Dry milk was removed by aspiration immediately before adding biotinylated CS-1. [1429] B. Binding of Biotinylated CS-1 to Isolated VLA-4 [1430] Biotinylated CS-1 peptide (bCS-1) was prepared. The peptide was diluted to a final concentration of 5 mg / ml with 1 mM MnCl (PBSB) containing PBS and 0.1% fat free dry milk. 200 ml aliquots were added to a well of a 96 well polypropylene delivery plate containing compound (32, 10, 3.2, 1, 0.32 and 0.1 mM), vehicle or antibody (0.5 mg / ml) in PBSB containing 0.1% DMSO for 60 minutes. (37 ° C.). The plate is washed three times with 200 ml / well PBSB to remove unbound bCS-1. Thereafter, 100 ml of a 1: 5000 dilution of streptavidin poly-HRP in PBSB was added to each well for 60 minutes (37 ° C.). Unbound streptavidin poly-HRP was removed by aspiration and the plates washed three times with PBSB (200 ml / well). After the final wash, 100 ml of TMB substrate was added to each well to react with bound streptavidinpoly-HRP, and the OD of each well on the plate was measured on an Emax plate reader (650). The results were based on the average of two measurements. [1431] Example 30 [1432] VLA-4 dependent THP1 cell binding to baculovirus sVCAM [1433] The THP1 baculovirus sVCAM cell binding assay tests the ability of compounds to inhibit VLA-4 dependent binding to sVCAM. [1434] A. Manufacture of sVCAM cladding [1435] The baculovirus sVCAM cladding was prepared the day before the experiment. The baculovirus sVCAM seed from PanVera was diluted to a final concentration of 5 mg / ml in 50 mM NaHCO 3 (pH 8.8). A 50 ml aliquot of the original seed solution was then added to each well of a 96 well microfluorine “B” U-shaped bottom plate (Dynatech No. 0010107205) and incubated overnight (4 ° C.). The coating solution was removed by aspiration and the wells were quenched for 1 hour using PBS (150 ml / well, 4 ° C.) containing 5% fat free milk. Dry milk is removed by shock dumping just prior to adding biotinylated CS-1. [1436] B. Labeling and Binding of THP1 Cells [1437] THP1 cells were obtained from the American Type Culture Collection (ATCC, Rockville, MD) and grown for 20 minutes (37 ° C.) in 10% 1 mM MnCl 2 containing RPMI 1640 medium. After MnCl 2 activity, cells were spun (about 500 g for 5 minutes) and resuspended twice in serum free basal medium (EBM, 37 ° C.). Cells in serum free medium (2 × 10 6 / ml) were incubated at 37 ° C. for 30 minutes using 5 mM calcein. After labeling, cells are rotated (about 500 g for 5 minutes) and resuspended twice in RPMI 1640 with 10% FBS to excise any free calcein AM. The cells were then resuspended twice in 1 mg / ml BAS containing DPBS (+1 mM CaCl 2 and 1 mM MgCl 2 ) (DPBSB) and diluted to 667,000 cells / ml. A 200 ml aliquot was placed in a well of a 96 well polypropylene delivery plate containing test compound (10, 5, 1 and 0.1 mM), vehicle or antibody (0.5 mg / ml) in DPBSB containing 0.1% DMSO for 30 minutes (37 ° C.). Was added. 150 ml (100,000 cells) were then removed from each well and delivered for 45 minutes (37 ° C.) into suitable wells of the quenched baculovirus sVCAM cladding. Unbound cells were removed by aspiration and the plates washed three times with DPBSB (100 ml / well). After the final wash, 100 ml of DPBSB was added to each well and the plates were read on a Cytoflour fluorescent plate reader. Three readings per well were made at 480 excitation and 530 releases. The results were based on the average of two measurements. The average background fluorescence of the blank wells was subtracted from each sample to obtain the corrected fluorescence intensity for each sample.
权利要求:
Claims (53) [1" claim-type="Currently amended] Compounds of Formula 1.0.0 and pharmaceutically acceptable salts and other prodrug derivatives thereof. Formula 1.0.0 Where A is (C 1 -C 6 ) alkyl, cycloalkyl, aryl, heteroaryl or heterocyclyl [these radicals are as defined herein and the radical alkyl, cycloalkyl, aryl, heteroaryl or heterocyclyl Optionally substituted with 0 to 3 substituents identical to R 9 , defined below; or A 1 -NHC (= 0) NH-A 2- , A 1 -NHC (= 0) OA 2- , A 1- OC (= O) NH-A 2- , A 1 -NHSO 2 NH-A 2- , A 1 -NHC (= O) -A 2- , A 1 -C (= O) NH-A 2- , A 1 -NHSO 2 -A 2- , A 1 -SO 2 NH-A 2- , A 1- (CH 2 ) r -A 2- , A 1 -CH (R 1 ) -OA 2- , A 1- ( CH 2 ) r OA 2- , A 1 -O (CH 2 ) r -A 2- , A 1- (CH 2 ) r NH-A 2- , A 1 -NH (CH 2 ) r -A 2- , And A 1- (CH 2 ) r S (= 0) q -A 2- , wherein A 1 and A 2 are each independently hydrogen, aryl, (C 1 -C 6 ) alkyl, (C 2 -C 6 ) Alkenyl, (C 2 -C 6 ) alkynyl, cycloalkyl, heteroaryl and heterocyclyl, wherein said aryl, alkyl, cycloalkyl, Heteroaryl or heterocyclyl group is a component selected from the group consisting of radicals of 0 to 3 substituents equal to R 9 defined below; B is a component independently selected from the group consisting of residues of the partial formulas 1.1.0 to 1.1.23; E is a single bond; -O-; -NR 10- , -CH = CH-, -C≡C-; -S (= 0) q- ; -CR 11 R 12 NR 10- ; Or -CR 11 R 12- ; X is -O-; -C (= 0)-; -S (= 0) q- ; Or -NR 10- ; X 1 , X 2 and X 3 are each independently CH; CR 9 ; And N; Y is a single bond; -C (= 0)-; -C (= S)-; Or -S (= 0) 2- ; k is an integer independently selected from 0, 1 and 2; m is an integer independently selected from 0 and 1; n is an integer independently selected from 0, 1 and 2; p is independently an integer of 0 or 1 and should be selected to 1 when B is selected as a residue of partial formula 1.1.0 to 1.1.11; q is an integer independently selected from 0, 1 and 2; r is an integer independently selected from 0, 1 and 2; R 1 is (C 1 -C 3 ) alkyl substituted with 0 or 1 F; CF 3 ; OCF 3 ; Or cyano; R 2 and R 3 are each independently hydrogen; A (C 1 -C 6) alkyl, optionally substituted by R 13 and the same 0 to 3 substituents as defined below (C 2 -C 6) optionally substituted with R 13 to define with the same 0 to 3 substituents alkenyl, defined below substituted with the same 0 to 3 substituents, and R 13 is (C 3 -C 14) carbocyclic ring system, the following definitions and R 13 is substituted by 0 to 3 substituents the same The same heterocyclyl ring as defined herein, substituted with (C 1 -C 6 ) alkyl-OR 5 , substituted with 0 to 3 substituents identical to R 13 as defined below, 0 to 3 R 13 (C 1 -C 6 ) alkyl-SR 5 , (C 1 -C 6 ) alkyl-SO 2 R 5 , 0 to 3 R substituted by 0 to 3 substituents the same as R 13 defined below 13 is substituted the same 0 and R 13 is the same heteroaryl ring, and to define as defined herein Which it is substituted by three substituents, and are each independently selected from the group consisting of the same aryl ring as defined herein; Provided that R 2 and R 3 are each the same as defined above; Together they form a ring defined below; One of which together with R 4 forms a group as defined below in which case the other is hydrogen or methyl; R 2 and R 3 together form a cycloalkyl or heterocyclyl ring substituted by 0 to 3 substituents same as R 13 , defined below; R 2 or R 3 is the same heteroaryl or heterocyclyl as defined herein and substituted by R 4 , and 0 to 3 substituents identical to R 13 , defined below, together with the carbon and nitrogen atoms to which they are attached, respectively; To form a group; R 4 is hydrogen; Or (C 1 -C 6 ) alkyl optionally substituted by the same substituent R 13 as defined below, or R 4 together with R 2 or R 3 form a carbocyclic or heterocyclic ring; R 5 and R 6 are independently hydrogen; Or (C 1 -C 6 ) alkyl; (C 2 -C 6 ) alkenyl; (C 2 -C 6 ) alkynyl; CF 3 ; Aryl; Cycloalkyl; Heteroaryl; Or heterocyclyl, wherein the alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heteroaryl or heterocyclyl is substituted by 0 to 3 substituents equal to R 13 defined below; R 7 is (C 1 -C 6 ) alkyl; (CH 2 ) k OR 5 ; (CH 2 ) k C (= 0) R 5 ; (CH 2 ) k C (= 0) NR 6 R 5 ; (CH 2 ) k NR 6 C (= 0) R 5 ; (CH 2 ) k NR 6 C (= 0) OR 5 ; (CH 2 ) k NR 6 SO 2 R 5 ; (CH 2 ) k NR 6 R 5 ; F; CF 3 ; OCF 3 ; Aryl substituted with 0 to 3 substituents identical to R 9 defined below; Heterocyclic substituted by 0 to 3 substituents equal to R 9 defined below; Heteroaryl substituted by 0 to 3 substituents the same as R 9 defined below; Or cycloalkyl substituted by 0 to 3 substituents equal to R 9 defined below; R 7 may form a cycloalkyl or heterocyclic ring with R 8 ; R 7 may form a cycloalkyl or heterocyclyl ring with R 11 ; R 8 is hydrogen; F; CN; (C 1 -C 6 ) alkyl or (C 1 -C 6 ) alkoxy; R 9 is hydrogen; (C 1 -C 6 ) alkyl; (C 1 -C 6 ) alkoxy; (C 3 -C 6 ) cycloalkyl; (C 3 -C 6 ) cycloalkoxy; Cyano; (CH 2 ) k OH; C (= 0) R 5 ; (CH 2 ) k C (O) NR 5 R 6 ; (CH 2 ) k NR 6 SO 2 R 5 ; CF 3 ; OCF 3 ; SO 2 NR 5 R 6 ; Or (CH 2 ) m C (= 0) OR 5 ; When R 9 is bonded to a saturated carbon atom R 9 may be = O or = S; R 9 may be ═O when R 9 is bonded to a sulfur atom; R 10 is hydrogen; C (= 0) R 5 ; C (= 0) OR 5 ; (C 1 -C 6 ) alkyl; Aryl; Heterocyclyl; Heteroaryl; Cycloalkyl; Or SO 2 R 5 ; R 11 and R 12 are independently -H; (C 1 -C 6 ) alkyl; -OH; -CN; (C 1 -C 6 ) alkoxy; NR 6 C (= 0) R 5 ; NR 6 SO 2 R 5 ; NR 6 R 5 ; CF 3 ; F; Aryl; Heterocyclyl; Heteroaryl; Cycloalkyl; Or cycloalkoxy; R 11 may form a cycloalkyl or heterocyclic ring with R 12 ; R 13 is halogen; CF 3 ; (C 1 -C 6 ) alkyl; Aryl; Heteroaryl; Heterocyclyl; Hydroxy; Cyano; (C 1 -C 6 ) alkoxy; (C 3 -C 6 ) cycloalkyl; (C 3 -C 6 ) cycloalkoxy; (C 2 -C 6 ) alkynyl; (C 2 -C 6 ) alkenyl; -NR 6 R 5 ; -C (= 0) NR 5 R 6 ; SO 2 R 5 ; C (= 0) R 5 ; NR 5 SO 2 R 6 ; NR 5 C (= 0) R 6 ; C (= 0) NR 5 SO 2 R 6 ; NR 5 C (= 0) OR 6 ; And SO 2 NR 6 R 5 . Chemical Formula 1.1.0 Formula 1.1.1 Formula 1.1.2 Formula 1.1.3 Chemical Formula 1.1.4 Formula 1.1.5 Formula 1.1.6 Chemical Formula 1.1.7 Chemical Formula 1.1.8 Formula 1.1.9 Formula 1.1.10 Formula 1.1.11 Formula 1.1.12 Formula 1.1.13 Formula 1.1.14 Formula 1.1.15 Formula 1.1.16 Formula 1.1.17 Formula 1.1.18 Formula 1.1.19 Formula 1.1.20 Formula 1.1.21 Formula 1.1.22 Formula 1.1.23 Where The indication of "*" indicates the point at which the moiety of each partial formula 1.1.0 to 1.1.23 binds to the residue "CR 2 R 3 " of formula 1.0.0, The indication of "→" indicates the point at which the moiety of each partial formula 1.1.0 to 1.1.23 binds to the residue "E" of formula 1.0.0, Residues of each partial formula 1.1.0 to 1.1.23 may be optionally substituted with R 9 except for the residues of partial formula 1.1.10, 1.1.17 and 1.1.23. [2" claim-type="Currently amended] The method of claim 1, If A is heteroaryl, furyl, thienyl, pyrrolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, imidazolyl, imidazolinyl, pyrazolyl, pyrazolinyl, oxdiazolyl thiadiazolyl , Triazolyl, pyridyl, pyrazinyl, pyridazinyl, pyrimidinyl, triazinyl, pyranyl, parathiazinyl, indolyl, isoindoleyl, 3H-indolyl, indolinyl, benzo [b] furanyl, 2,3-dihydrobenzofuranyl, benzo [b] thiophenyl, 1H-indazolyl, benzimidazolyl, benzoxazolyl, benzthiazolyl, furinyl, quinolinyl, isoquinolinyl, 4H-qui Nolininyl, cynolinyl, phthalazinyl, quinazolinyl, quinoxalinyl, 1,8-naphthyridinyl, pterridinyl, carbazolyl, acridinyl, phenazinyl, phenthiazinyl, phenoxazinyl, and A compound selected from the group consisting of pyrazolol [1,5-c] triazinyl. [3" claim-type="Currently amended] The method of claim 2, A is furyl, thienyl, pyrrolyl, oxazolyl, isoxazolyl, thiazolyl, imidazolyl, pyridyl, pyrimidinyl, indolyl, benzo [b] furanyl, benzimidazolyl or quinolinyl compound. [4" claim-type="Currently amended] The method of claim 3, wherein A is pyridyl. [5" claim-type="Currently amended] The method of claim 1, When A is heterocyclyl oxiranyl, pyrrolidinyl, pyrazolidinyl, imidazolidinyl, tetrazolidinyl, piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl and benzodioxolane and 1, A compound selected from the group consisting of 3-benzodioxol-5-yl. [6" claim-type="Currently amended] The method of claim 5, A is pyrrolidinyl, piperidinyl, piperazinyl or morpholinyl. [7" claim-type="Currently amended] The method of claim 1, A is A 1 -NHC (= O) NH-A 2- , A 1 -NHC (= O) OA 2- , A 1 -OC (= O) NH-A 2- , A 1 -NHSO 2 NH-A 2- , A 1 -NHC (= O) -A 2- , A 1 -C (= O) NH-A 2- , A 1 -NHSO 2 -A 2- , A 1 -SO 2 NH-A 2- , A 1- (CH 2 ) r -A 2- , A 1 -CH (R 1 ) -OA 2- , A 1- (CH 2 ) r OA 2- , A 1 -O (CH 2 ) r -A 2- , A 1- (CH 2 ) r NH-A 2- , A 1 -NH (CH 2 ) r -A 2- , and A 1- (CH 2 ) r S (= O) q -A 2- Wherein A 1 and A 2 are each independently hydrogen, aryl, (C 1 -C 6 ) alkyl, (C 2 -C 6 ) alkenyl, (C 2 -C 6 ) alkynyl, cycloalkyl, heteroaryl And heterocyclyl, wherein the aryl, alkyl, alkenyl, cycloalkyl, heteroaryl or heterocyclyl group is substituted with 0 to 3 R 9 radicals. [8" claim-type="Currently amended] The method of claim 7, wherein A 1 and A 2 are both aryl or heteroaryl. [9" claim-type="Currently amended] The method of claim 8, Aryl is phenyl, heteroaryl is pyridyl, and each of these components is F; Cl; F 3 C-; methyl; Methoxy; Hydroxy; Iso-propyl; Cyclopropyloxy; And 0 or 1 substituent R 9 independently selected from the group consisting of cyclopentyl. [10" claim-type="Currently amended] The method of claim 9, A compound wherein n is an integer of 1 and forms a methylene bridge. [11" claim-type="Currently amended] The method of claim 10, Component A and the methylene crosslinked attached thereto are 4-hydroxyphenyl-; 3-methoxy-4- (N'-phenylurea) phenylmethyl-; 4- (N'-phenylurea) -phenylmethyl-; 4- [N '-(2-methylphenyl) urea] -phenylmethyl-; 4- [N '-(2-methoxyphenyl) urea] -phenylmethyl-; 3-methoxy-4- [N '-(2-methylphenyl) urea] -phenylmethyl-; 4- [N '-(2-pyridyl) urea] -phenylmethyl-; 6-methoxy-5- [N '-(2-methylphenyl) urea] -2-pyridylmethyl-; 4- [N '-(3-methyl-2-pyridyl) urea] -phenylmethyl-; 3-methoxy-4- [N '-(3-methyl-2-pyridyl) urea] -phenylmethyl-; 3-methoxy-4- [N '-(2-pyridyl) urea] -phenylmethyl-; 4- [N '-(2-pyridyl) urea] -phenylmethyl-; 4- [N '-(2-fluorophenyl) urea] -phenylmethyl-; 4- [N '-(2-chlorophenyl) urea] -phenylmethyl-; 4- [N '-(2-chlorophenyl) urea] -3-methoxyphenylmethyl-; 4- [N '-(4-iso-propylphenyl) urea] -phenylmethyl-; 6-methoxy-5- [N '-(o-toluyl) urea] -2-pyridylmethyl-; 4- [N '-(3-cyclopropyloxy-2-pyridyl) urea] -phenylmethyl-; And 4- [N '-(o-toluyl) urea] -pyrid-5-ylmethyl-. [12" claim-type="Currently amended] The method of claim 9, Y is -C (= 0)-. [13" claim-type="Currently amended] The method of claim 12, When the component of Formula 1.0.0 is -NR 4 CR 2 CR 3- , all of R 2 to R 4 are hydrogen; [14" claim-type="Currently amended] The method of claim 12, When the component of Formula 1.0.0 is —NR 4 CR 2 CR 3 —, R 2 and R 4 are both hydrogen and R 3 is iso-butyl. [15" claim-type="Currently amended] The method of claim 12, R 2 and R 3 are both hydrogen when the component of formula 1.0.0 is —NR 4 CR 2 CR 3- . [16" claim-type="Currently amended] The method of claim 12, When the component of Formula 1.0.0 is —NR 4 CR 2 CR 3 —, R 2 and R 3 are both hydrogen and R 4 is methyl. [17" claim-type="Currently amended] The method of claim 12, When the component of Formula 1.0.0 is -NR 4 CR 2 CR 3- , R 4 together with R 2 or R 3 forms pyrrolidinyl such that R 4 is methylene or ethylene and one of R 2 and R 3 is hydrogen; The other of R 2 and R 3 is ethylene or methylene. [18" claim-type="Currently amended] The method of claim 12, B is a component selected from the group consisting of the residues of the partial formulas 1.1.2, 1.1.6, 1.1.17, 1.1.18, 1.1.19 and 1.1.22. Formula 1.1.2 Formula 1.1.6 Formula 1.1.17 Formula 1.1.18 Formula 1.1.19 Formula 1.1.22 Where The indications of "*" and "→" are the same as defined in claim 1, X is oxygen, S (= 0) q or nitrogen; X 1 , X 2 and X 3 are each independently —CH—; -CR 9- ; And -N-. [19" claim-type="Currently amended] The method of claim 18, B is a moiety of the partial formula 1.1.6. [20" claim-type="Currently amended] The method of claim 19, Partial a compound of which X is -O- at the residue of formula 1.1.6. [21" claim-type="Currently amended] The method of claim 18, B is a moiety of the partial formula 1.1.22. [22" claim-type="Currently amended] The method of claim 21, At the residue of formula 1.1.22, wherein X is —NR 10 —, wherein R 10 is —H and X 1 , X 2 and X 3 are each —CH—. [23" claim-type="Currently amended] The method of claim 12, p is 1; m is 0 or 1; E is -CR 11 R 12- . [24" claim-type="Currently amended] The method of claim 23, p is 1; m is 0; R 11 is -H; R 12 is -H. [25" claim-type="Currently amended] The method of claim 1, A compound which is a compound comprising a moiety of the partial formula 1.1.0: 3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4,5-dihydro -Oxazol-5-yl] -2-methyl-propionic acid; 2-acetylamino-3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4 , 5-dihydro-oxazol-5-yl] -propionic acid; 2-methanesulfonylamino-3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4,5-dihydro-oxazol-5-yl] -propionic acid; 2,2-difluoro-3- {2- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- 4,5-dihydro-oxazol-5-yl} -propionic acid; 2,2-dimethyl-3- [2- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -4,5- Dihydro-oxazol-5-yl] -propionic acid; 2-allyloxycarbonylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4 , 5-dihydro-oxazol-5-yl} -propionic acid; 2- (butane-1-sulfonylamino) -3- (2-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -4,5-dihydro-oxazol-5-yl) -propionic acid; 2-Methyl-3- [2- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -4,5-dihydro-oxazole- 5-yl] -propionic acid, 2-formylamino-3- {2- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -4,5-dihydro-thiazol-5-yl} -propionic acid , 2-methyl-3- (2- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -4,5-dihydro-oxazol-5-yl) Propionic acid, 2-benzenesulfonylamino-3- (2- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -4,5-dihydro-oxazole-5- Yl) -propionic acid, 2-benzenesulfonylamino-3- [2- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- 4,5-dihydro-oxazol-5-yl] -propionic acid, 2-methanesulfonylamino-3- [2- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -4,5-dihydro-oxazol-5-yl] -propionic acid, 2-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4-methyl- 4,5-dihydro-oxazol-5-yl} -propionic acid, 2-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4,5- Dihydro-thiazol-3-yl} -propionic acid, 3-acetylamino-3- {2-[({[3-methoxy-4- (3-otolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4,5-di Hydro-3H-imidazol-4-yl} -propionic acid, and 2- (2,6-Dichloro-benzoylamino) -3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -4,5-dihydro-oxazol-5-yl} -propionic acid. [26" claim-type="Currently amended] The method of claim 1, A compound which is a compound comprising a moiety of the partial formula 1.1.1: 3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4,5-dihydro -Oxazol-4-yl] -2-methyl-propionic acid, 2-acetylamino-3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4 , 5-dihydro-oxazol-4-yl] -propionic acid, 2-methanesulfonylamino-3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4,5-dihydro-oxazol-4-yl] -propionic acid, 2,2-difluoro-3- {2- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} amino) -ethyl] -4 , 5-dihydro-oxazol-4-yl} -propionic acid, 2,2-dimethyl-3- [2- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -4,5- Dihydro-oxazol-4-yl] -propionic acid, 2-allyloxycarbonylamino-3- {2-[({(3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4 , 5-dihydro-oxazol-4-yl} -propionic acid, 2- (butane-1-sulfonylamino) -3- (2-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -4,5-dihydro-oxazol-4-yl) -propionic acid, 2-Methyl-3- [2- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -4,5-dihydro-oxazole- 4-yl] -propionic acid, 2-acetylamino-3- {2- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -4,5-dihydro-thiazol-4-yl} -propionic acid, 2-methyl-3- (2- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -4,5-dihydro-oxazol-4-yl) Propionic acid, 2-benzenesulfonylamino-3- (2- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -4,5-dihydro-oxazole-4- Yl) -propionic acid, 2-benzenesulfonylamino-3- [2- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- 4,5-dihydro-oxazol-4-yl] -propionic acid, 2-methanesulfonylamino-3- [2- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -4,5-dihydro-oxazol-4-yl] -propionic acid, 2-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- 4,5-dihydro-oxazol-4-yl} -propionic acid, 2-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4,5- Dihydro-thiazol-4-yl} -propionic acid, and 2- (2,6-Dichloro-benzoylamino) -3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -4,5-dihydro-oxazol-4-yl} -propionic acid. [27" claim-type="Currently amended] The method of claim 1, A compound which is a compound comprising a moiety of the partial formula 1.1.2: 3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -oxazol-5-yl ] -2-methyl-propionic acid, 2-acetylamino-3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -oxa Sol-5-yl] -propionic acid, 2-methanesulfonylamino-3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Oxazol-5-yl] -propionic acid, 2,2-difluoro-3- {2- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Oxazol-5-yl} -propionic acid, 2,2-Dimethyl-3- [2- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -oxazole-5 -Yl] -propionic acid, 2-allyloxycarbonylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -oxa Sol-5-yl} -propionic acid, 2- (butane-1-sulfonylamino) -3- (2-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -oxazol-5-yl) -propionic acid, 2-Methyl-3- [2- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -oxazol-5-yl] -propionic acid, 2-acetylamino-3- {2- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -thiazol-5-yl} -propionic acid, 2-Methyl-3- (2- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-3-yl} -oxazol-5-yl) -propionic acid, 2-benzenesulfonylamino-3- (2- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -oxazol-5-yl) -propionic acid, 2-benzenesulfonylamino-3- [2- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Oxazol-5-yl] -propionic acid, 2-methanesulfonylamino-3- [2- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -oxazol-5-yl] -propionic acid, 2-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4-methyl- Oxazol-5-yl} -propionic acid, 2-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -thiazole-5 -Yl} -propionic acid, 3-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -3H-imidazole -4-yl} -propionic acid, and 2- (2,6-Dichloro-benzoylamino) -3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -oxazol-5-yl} -propionic acid. [28" claim-type="Currently amended] The method of claim 1, A compound which is a compound comprising a moiety of the partial formula 1.1.3: 3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl} -oxazol-4-yl ] -2-methyl-propionic acid, 2-acetylamino-3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -oxa Zol-4-yl] -propionic acid, 2-methanesulfonylamino-3- [2- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Oxazol-4-yl] -propionic acid, 2,2-difluoro-3- {2- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Oxazol-4-yl} -propionic acid, 2,2-dimethyl-3- [2- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -oxazole-4 -Yl] -propionic acid, 2-allyloxycarbonylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -oxa Zol-4-yl} -propionic acid, 2- (butane-1-sulfonylamino) -3- (2-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -oxazol-4-yl) -propionic acid, 2-Methyl-3- [2- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -oxazol-4-yl] -propionic acid, 2-formylamino-3- {2- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -thiazol-4-yl} -propionic acid, 2-Methyl-3- (2- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -oxazol-4-yl) -propionic acid, 2-benzenesulfonylamino-3- (2- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -oxazol-4-yl) -propionic acid, 2-benzenesulfonylamino-3- [2- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Oxazol-4-yl] -propionic acid, 2-methanesulfonylamino-3- [2- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -oxazol-4-yl] -propionic acid, 2-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- Oxazol-4-yl} -propionic acid, 2-acetylamino-3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -thiazole-4 -Yl} -propionic acid, 2- (2,6-Dichloro-benzoylamino) -3- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -oxazol-4-yl} -propionic acid, 3- [2- (1-{[4- (4-Chloro-benzyloxy) -3-fluoro-phenyl] -acetyl} -pyrrolidin-2-yl) -thiazol-5-yl] -propionic acid , 3- [2- (1-{[3-Fluoro-4- (3-methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -thiazol-5-yl]- Propionic Acid, 3- [2- (1-{[3-Chloro-4- (4-chloro-benzoyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -thiazol-5-yl] -propionic acid, 3- [2- (1-{[4- (4-Chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -thiazol-5-yl] -propionic acid, 3- (2- {1-[(4-benzyloxy-3-chloro-phenyl) -acetyl] -3-methyl-pyrrolidin-2-yl} -thiazol-5-yl) -propionic acid, 3- [2- (1-{[4- (4-Chloro-benzyloxy) -phenyl] -acetyl} -3-methyl-pyrrolidin-2-yl) -thiazol-5-yl] -propionic acid, 3- (2- {1-[(4-benzyloxy-phenyl) -acetyl] -3-methyl-pyrrolidin-2-yl} -thiazol-5-yl) -propionic acid, 3- (2- {1-[(4-benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -thiazol-5-yl) -propionic acid, and 3- (2- {1-[(4-Benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid. [29" claim-type="Currently amended] The method of claim 1, A compound comprising a moiety of the partial formula 1.1.4 and selected from the group consisting of 3- [3- (1- (2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4,5-dihydro Isoxazol-5-yl] -2-methyl-propionic acid, 2-acetylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4 , 5-dihydro-isoxazol-5-yl] -propionic acid, 2-methanesulfonylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4,5-dihydro-isoxazol-5-yl] -propionic acid, 2,2-difluoro-3- {3- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- 4,5-dihydro-isoxazol-5-yl} -propionic acid, 2,2-dimethyl-3- [3- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -4,5- Dihydro-isoxazol-5-yl] -propionic acid, 2-allyloxycarbonylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4 , 5-dihydro-isoxazol-5-yl} -propionic acid, 2- (butane-1-sulfonylamino) -3- (3-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl) -acetyl) -amino] -methyl} -4,5-dihydro-isoxazol-5-yl) -propionic acid, 2-Methyl-3- [3- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -4,5-dihydro-isoxazole- 5-yl] -propionic acid, 2-formylamino-3- {3- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -4,5-dihydro-isothiazol-5-yl}- Propionic Acid, 2-methyl-3- (3- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -4,5-dihydro-isoxazol-5-yl) Propionic acid, 2-benzenesulfonylamino-3- (3- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -4,5-dihydro-isoxazole-5- Yl) -propionic acid, 2-benzenesulfonylamino-3- [3- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- 4,5-dihydro-isoxazol-5-yl] -propionic acid, 2-methanesulfonylamino-3- [3- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -4,5-dihydro-isoxazol-5-yl] -propionic acid, 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4-methyl- 4,5-dihydro-isoxazol-5-yl) -propionic acid, 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4,5- Dihydro-isothiazol-5-yl} -propionic acid, 3-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -3,4- Dihydro-2H-pyrazol-3-yl} -propionic acid, and 2- (2,6-Dichloro-benzoylamino) -3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -4,5-dihydro-isoxazol-5-yl} -propionic acid. [30" claim-type="Currently amended] The method of claim 1, A compound comprising a moiety of the partial formula 1.1.5 and selected from the group consisting of: 3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4,5-dihydro -Pyrazol-1-yl] -2-methyl-propionic acid, 2-acetylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4 , 5-dihydro-pyrazol-1-yl] -propionic acid, 2-methanesulfonylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -4,5-dihydro-pyrazol-1-yl] -propionic acid, 2,2-difluoro-3- {3- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- 4,5-dihydro-pyrazol-1-yl} -propionic acid, 2,2-dimethyl-3- [3- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -4,5- Dihydro-pyrazol-1-yl] -propionic acid, 2- (butane-1-sulfonylamino) -3- (3-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -4,5-dihydro-pyrazol-1-yl) -propionic acid, 2-Methyl-3- [3- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -4,5-dihydro-pyrazole- 1-yl] -propionic acid, 2-acetylamino-3- {3- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -4,5-dihydro-pyrazol-1-yl} -propionic acid, 2-methyl-3- (3- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -4,5-dihydro-pyrazol-1-yl) Propionic acid, 2-benzenesulfonylamino-3- (3- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -4,5-dihydro-pyrazole-1- Il-propionic acid, 2-benzenesulfonylamino-3- [3- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- 4,5-dihydro-pyrazol-1-yl] -propionic acid, 2-methanesulfonylamino-3- [3- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -4,5-dihydro-pyrazol-1-yl] -propionic acid, 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- 4,5-dihydro-pyrazol-yl} -propionic acid, 2-formylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4,5 -Dihydro-pyrazol-1-yl} -propionic acid, and 2- (2,6-Dichloro-benzoylamino) -3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -4,5-dihydro-pyrazol-1-yl} -propionic acid. [31" claim-type="Currently amended] The method of claim 1, A compound comprising a moiety of the partial formula 1.1.6 and selected from the group consisting of: 3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -isoxazole-5- General] -2-methyl-propionic acid, 2-acetylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -isoxo Sazol-5-yl] -propionic acid, 2-methanesulfonylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) Isoxazol-5-yl] -propionic acid, 2,2-difluoro-3- {3- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Isoxazol-5-yl} -propionic acid, 2,2-dimethyl-3- [3- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -isoxazole-5 -Yl] -propionic acid, 2-allyloxycarbonylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl} -methyl] -methyl Sazol-5-yl} -propionic acid, 2- (butane-1-sulfonylamino) -3- (3-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl) -acetyl) -amino] -methyl} -isoxazol-5-yl) -propionic acid, 2-Methyl-3- [3- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 2-acetylamino-3- {3- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -isothiazol-5-yl} -propionic acid, 2-Methyl-3- (3- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, 2-benzenesulfonylamino-3- (3- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, 2-benzenesulfonylamino-3- [3- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Isoxazol-5-yl] -propionic acid, 2-methanesulfonylamino-3- [3- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -isoxazol-5-yl] -propionic acid, 2-formylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4-methyl Isoxazole-5-yl} -propionic acid, 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -isothiazole- 5-yl} -propionic acid, 3-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -2H-pyrazole -3-yl} -propionic acid, 2- (2,6-Dichloro-benzoylamino) -3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -isoxazol-5-yl} -propionic acid, 3- [3- (1-{[4- (pyridin-4-ylmethoxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- [3- (1-{[4- (pyridin-3-ylmethoxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- [3- (1-{[4- (pyridin-2-ylmethoxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- (3- {1-[(6-benzyloxy-pyridin-3-yl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, 3- (3- {1-[(5-benzyloxy-pyridin-2-yl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, 3- (3- {1-[(4-benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -2-phenylamino-propionic acid, 3- (3- {1-[(4-Benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -2- (pyridin-2-ylamino) -propionic acid , 3- (3- {1-[(4-Benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -2- (pyridin-3-ylamino) -propionic acid , 3- (3- {1-[(4-Benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -2- (pyridin-4-ylamino) -propionic acid , 3- [3- (1-{[4- (5-Chloro-thiophen-2-ylmethoxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid , 3- (3- {1-[(4-benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, 3- (3- {1-{[4-Chloro-benzyloxy) -3-fluoro-phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- [3- (1-{[3-Fluoro-4- (3-methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl]- Propionic Acid, Phenyl]-(propane-1-sulfonylamino) -propionic acid, 3- [3- (1-{[3-methoxy-4- (4-methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl]- Propionic Acid, 3- [3- (1-{[3-methoxy-4- (3-methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl]- Propionic Acid, 3- [3- (1-{[4- (4-Chloro-benzyloxy) -3-methoxy-phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid , 3- [3- (1-{[4- (3-Chloro-benzyloxy) -3-methoxy-phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid , 3- [3- (1-{[4- (2-Chloro-benzyloxy) -3-methoxy-phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid , 3- [3- (1-{[4- (4-Fluoro-benzyloxy) -3-methoxy-phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl]- Propionic Acid, 3- [3- (1-{[4- (3-Fluoro-benzyloxy) -3-methoxy-phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl]- Propionic Acid, 3- [3- (1-{[4- (2-Fluoro-benzyloxy) -3-methoxy-phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl]- Propionic Acid, 3- [3- (1-{[3-Chloro-4- (3-methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid , 2-acetylamino-3- [3- (1-{[3-chloro-4- (3-methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazole-5 -Yl] -propionic acid, 2-acetylamino-3- (3- {1-[(4-benzyloxy-3-methoxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, 3- [3- (1-{[4- (5-tert-butyl- [1,2,4] oxadiazol-3-ylmethoxy) -phenyl] -acetyl} -pyrrolidin-2-yl) Isoxazol-5-yl] -propionic acid, 2-acetylamino-3- [3- (1-{[3-chloro-4- (4-chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazole-5- General] -propionic acid, 3- [3- (1-{[3-Chloro-4- (4-chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- [3- (1-{[4- (2-Cyano-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- [3- (1-{[4- (4-Cyano-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- (3- {1-[(4-benzyloxy-3-fluoro-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, 3- (3- {1-[(4-benzyloxy-3-chloro-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, 3- (3- {1- [2- (4-benzyloxy-phenyl) -acetylamino] -3-methyl-butyl} -isoxazol-5-yl) -propionic acid, 2-acetylamino-3- [3- (1-{[4- (3-cyano-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl]- Propionic Acid, 2-acetylamino-3- [3- (1-{[4- (4-chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid , 2-acetylamino-3- (3- {1-[(4-benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, 3- (3- {1-[(4-p-tolyloxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, 3- (3- {1-[(4-m-tolyloxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, 3- (3- {1-[(4-o-tolyloxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, 3- [3- (1-{(4- (4-Methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, 3- [3- (1-{[4- (3-methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- [3- (1-{(4- (2-Methoxy-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 2-acetylamino-3- [3- (3-methyl-1- {2- [4- (2-methyl-benzyloxy) -phenyl] -acetylamino} -butyl) -isoxazol-5-yl]- Propionic Acid, 2-acetylamino-3- (3- {1- [2- (4-benzyloxy-phenyl) -acetylamino] -3-methyl-butyl} -isoxazol-5-yl) -propionic acid, 3- [3- (1-{[4- (4-Fluoro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- [3- (1-{[4- (3-Fluoro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- [3- (1-{[4- (2-Fluoro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- [3- (1-{[4- (2-Chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- [3- (1-{[4- (3-Chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- [3- (1-{[4- (4-Chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- [3- (1-{[4- (3-Methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- [3- (1-{[4- (4-Methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- [3- (1-{[4- (2-Methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- (3- {3-Methyl-1- [2- (4-phenoxy-phenyl) -acetylamino] -butyl} -isoxazol-5-yl) -propionic acid, 2-allyloxycarbonylamino-3- [3- (1-benzoyl-pyrrolidin-2-yl) -isoxazol-5-yl] -propionic acid, 3- (3- {1-[(4-benzyloxy-3-methoxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-5-yl) -propionic acid, 3- (5- {1-[(4-benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -2H-pyrazol-3-yl) -propionic acid, 3- (3- {1- [3- {2-Methyl-benzyloxy) -benzoyl] -pyrrolidin-2-yl) -isoxazol-5-yl) -propionic acid, 3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -oxazol-2-yl ] -2-methyl-propionic acid, 2-acetylamino-3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -oxa Zol-2-yl] -propionic acid, 2-methanesulfonylamino-3- [5- (1- {2- [3-methoxy-4- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino } -3-methyl-butyl) -oxazol-2-yl] -propionic acid, 2-methanesulfonylamino-3- [3- (1- {2- [3-methoxy-4- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino } -3-methyl-butyl) -pyrazol-1-yl] -propionic acid, 2,2, -difluoro-3- {3- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl] -Pyrazol-1-yl} -propionic acid, 2,2-dimethyl-3- [3- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -pyrazole-1 -Yl] -propionic acid, 2- (butane-1-sulfonylamino) -3- (3-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -pyrazol-2-yl) -propionic acid, 2-Methyl-3- [3- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -pyrazol-1-yl] -propionic acid, 2-formylamino-3- {3- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -pyrazol-1-yl} -propionic acid, 2-Methyl-3- (3- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -pyrazol-1-yl) -propionic acid, 2-benzenesulfonylamino-3- (3- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -pyrazol-1-yl) -propionic acid, 2-benzenesulfonylamino-3- [3- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Pyrazol-1-yl] -propionic acid, 2-methanesulfonylamino-3- [3- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -pyrazol-1-yl] -propionic acid, 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- Pyrazol-1-yl} -propionic acid, 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -pyrazole-1 -Yl} -propionic acid, and 2- (2,6-Dichloro-benzoylamino) -3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -pyrazol-1-yl} -propionic acid. [32" claim-type="Currently amended] The method of claim 1, A compound comprising a moiety of the partial formula 1.1.7 and a component selected from the group consisting of: 3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -pyrazol-1-yl ] -2-methyl-propionic acid, 2-acetylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -pyra Zol-1-yl] -propionic acid, 2-methanesulfonylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Pyrazol-1-yl] -propionic acid, 2,2-difluoro-3- {3- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Pyrazol-1-yl} -propionic acid, 2,2-dimethyl-3- [3- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -pyrazole-1 -Yl] -propionic acid, 2- (butane-1-sulfonylamino) -3- (3-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -pyrazol-1-yl) -propionic acid, 2-Methyl-3- [3- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -pyrazol-1-yl] -propionic acid, 2-formylamino-3- {3- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -pyrazol-1-yl} -propionic acid, 2-Methyl-3- (3- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -pyrazol-1-yl) -propionic acid, 2-benzenesulfonylamino-3- (3- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -pyrazol-1-yl) -propionic acid, 2-benzenesulfonylamino-3- [3- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Pyrazol-1-yl] -propionic acid, 2-methanesulfonylamino-3- [3- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -pyrazol-1-yl] -propionic acid, 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- Pyrazol-1-yl} -propionic acid, 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -pyrazole-1 -Yl} -propionic acid, and 2- (2,6-Dichloro-benzoylamino) -3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -pyrazol-1-yl} -propionic acid. [33" claim-type="Currently amended] The method of claim 1, A compound which is a compound which comprises a moiety of the partial formula 1.1.8: 3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -oxazol-2-yl ] -2-methyl-propionic acid, 2-acetylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -oxa Zol-2-yl] -propionic acid 2-methanesulfonylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Oxazol-2-yl] -propionic acid, 2,2-difluoro-3- {4- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Oxazol-2-yl} -propionic acid, 2,2-dimethyl-3- [4- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -oxazole-2 -Yl] -propionic acid, 2-allyloxycarbonylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -oxa Zol-2-yl} -propionic acid, 2- (butane-1-sulfonylamino) -3- (4-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -oxazol-2-yl) -propionic acid, 2-Methyl-3- [4- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -oxazol-2-yl] -propionic acid, 2-formylamino-3- {4- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -thiazol-2-yl} -propionic acid, 2-Methyl-3- (4- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -oxazol-2-yl) -propionic acid, 2-benzenesulfonylamino-3- (4- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -oxazol-2-yl) -propionic acid, 2-benzenesulfonylamino-3- [4- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Oxazol-2-yl] -propionic acid, 2-methanesulfonylamino-3- [4- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -oxazol-2-yl] -propionic acid, 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- Oxazol-2-yl} -propionic acid, 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -thiazole-2 -Yl} -propionic acid, 2- (2,6-Dichloro-benzoylamino) -3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -oxazol-2-yl} -propionic acid, and 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -1 H-imidazole -2-yl} -propionic acid. [34" claim-type="Currently amended] The method of claim 1, A compound which is a compound comprising a moiety of the partial formula 1.1.9: 3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -imidazol-1-yl ] -2-methyl-propionic acid, 2-acetylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -already Dazol-1-yl] -propionic acid, 2-methanesulfonylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Imidazol-1-yl] -propionic acid, 2,2-difluoro-3- {4- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Imidazol-1-yl} -propionic acid, 2,2-dimethyl-3- [4- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -imidazole-1 -Yl] -propionic acid, 2- (butane-1-sulfonylamino) -3- (4-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -imidazol-1-yl) -propionic acid, 2-Methyl-3- [4- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -imidazol-1-yl] -propionic acid, 2-formylamino-3- {4- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -imidazol-1-yl} -propionic acid, 2-Methyl-3- (4- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -imidazol-1-yl) -propionic acid, 2-benzenesulfonylamino-3- (4- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -imidazol-1-yl) -propionic acid, 2-benzenesulfonylamino-3- [4- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Imidazol-1-yl] -propionic acid, 2-methanesulfonylamino-3- [4- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -imidazol-1-yl] -propionic acid, 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- Imidazol-1-yl} -propionic acid, 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -imidazole-1 -Yl} -propionic acid, and 2- (2,6-Dichloro-benzoylamino) -3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -imidazol-1-yl} -propionic acid. [35" claim-type="Currently amended] The method of claim 1, A compound which is a compound comprising a moiety of the partial formula 1.1.10: 3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl)-[1,2,4 ] Oxadiazol-5-yl] -2-methyl-propionic acid, 2-acetylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl)-[ 1,2,4] oxadiazol-5-yl] -propionic acid, 2-methanesulfonylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -[1,2,4] oxadiazol-5-yl] -propionic acid, 2,2-difluoro-3- {3- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- [1,2,4] oxadiazol-5-yl} -propionic acid, 2,2-dimethyl-3- [3- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl)-[1,2 , 4] oxadiazol-5-yl] -propionic acid, 2-allyloxycarbonylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl]-[ 1,2,4] oxadiazol-5-yl} -propionic acid, 2- (butane-1-sulfonylamino) -3- (3-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl}-[1,2,4] oxadiazol-5-yl) -propionic acid, 2-methyl-3- [3- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl)-[1,2,4] oxadiazole -5-yl] -propionic acid, 2-formylamino-3- {3- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl]-[1,2,4] thiadiazol-5-yl}- Propionic Acid, 2-methyl-3- (3- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl}-[1,2,4] oxadiazol-5-yl ) -Propionic acid, 2-benzenesulfonylamino-3- (3- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl}-[1,2,4] oxidazol-5 -Yl) -propionic acid, 2-benzenesulfonylamino-3- [3- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- [1,2,4] oxadiazol-5-yl] -propionic acid, 2-methanesulfonylamino-3- [3- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl)-[1,2,4] oxadiazol-5-yl] -propionic acid, 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl- [1,2, 4] oxadiazol-5-yl} -propionic acid, 2-formylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl]-[1, 2,4] thiadiazol-5-yl} -propionic acid, 3-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -2H- [1 , 2,4] thiazol-3-yl} -propionic acid, and 2- (2,6-Dichloro-benzoylamino) -3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl]-[1,2,4] oxadiazol-5-yl} -propionic acid. [36" claim-type="Currently amended] The method of claim 1, A compound which is a compound comprising a moiety of the partial formula 1.1.11: 3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl)-[1,2,4 ] Triazol-1-yl] -2-methyl-propionic acid, 2-acetylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl)-[ 1,2,4] triazol-1-yl] -propionic acid, 2-methanesulfonylamino-3- [3- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -[1,2,4] triazol-1-yl] -propionic acid, 2,2-difluoro-3- {3- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- [1,2,4] triazol-1-yl} -propionic acid, 2,2-dimethyl-3- [3- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl)-[1,2 , 4] triazol-1-yl] -propionic acid, 2-allyloxycarbonylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl]-[ 1,2,4] triazol-1-yl} -propionic acid, 2- (butane-1-sulfonylamino) -3- (3-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl}-[1,2,4] triazol-1-yl) -propionic acid, 2-Methyl-3- [3- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl)-[1,2,4] triazole- 1-yl] -propionic acid, 2-acetylamino-3- {3- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl]-[1,2,4] triazol-1-yl} -propionic acid, 2-methyl-3- (3- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl}-[1,2,4] triazol-1-yl) Propionic acid, 2-benzenesulfonylamino-3- (3- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl}-[1,2,4] triazole-1- Yl) -propionic acid, 2-benzenesulfonylamino-3- [3- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- [1,2,4] triazol-1-yl] -propionic acid, 2-methanesulfonylamino-3- [3- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl)-[1,2,4] triazol-1-yl] -propionic acid, 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4-methyl- [1,2,4] triazol-1-yl} -propionic acid, 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl]-[1,2 , 4] triazol-1-yl} -propionic acid, and 2- (2,6-Dichloro-benzoylamino) -3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl]-[1,2,4] triazol-1-yl} -propionic acid. [37" claim-type="Currently amended] The method of claim 1, Compounds which are the following compounds comprising a moiety of the partial formula 1.1.12: 3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -thiophen-2-yl ] -2-methyl-propionic acid, 2-acetylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -furan -2-yl] -propionic acid, 2-methanesulfonylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Thiophen-2-yl] -propionic acid, 2,2-difluoro-3- {4- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- 1H-pyrrole-2-yl} -propionic acid, 2,2-Dimethyl-3- [4- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -thiophene-2 -Yl] -propionic acid, 2- (butane-1-sulfonylamino) -3- (4-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -furan-2-yl) -propionic acid, 2-Methyl-3- [4- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -1 H-pyrrol-2-yl] -propionic acid , 2-formylamino-3- [4- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -thiophen-2-yl} -propionic acid, 2-Methyl-3- (4- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -1 H-pyrrol-2-yl) -propionic acid, 2-benzenesulfonylamino-3- (4- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -furan-2-yl) -propionic acid, 2-benzenesulfonylamino-3- [4- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Thiophen-2-yl] -propionic acid, 2-methanesulfonylamino-3- [4- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -1H-pyrrol-2-yl] -propionic acid, 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- 1H-pyrrole-2-yl} -propionic acid, 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -thiophene-2 -Yl} -propionic acid, and 2- (2,6-Dichloro-benzoylamino)-{4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl ] -Furan-2-yl} -propionic acid. [38" claim-type="Currently amended] The method of claim 1, A compound which is a compound comprising a moiety of the partial formula 1.1.13: 3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -thiophen-3-yl ] -2-methyl-propionic acid, 2-acetylamino-3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -furan -3-yl] -propionic acid, 2-methanesulfonylamino-3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Thiophen-3-yl] -propionic acid, 2,2-difluoro-3- {5- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- 1H-pyrrole-3-yl} -propionic acid, 2,2-dimethyl-3- [5- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -thiophene-3 -Yl] -propionic acid, 2- (butane-1-sulfonylamino) -3- (5-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -furan-3-yl) -propionic acid, 2-Methyl-3- [5- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -1 H-pyrrol-3-yl] -propionic acid , 2-formylamino-3- {5- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -thiophen-3-yl} -propionic acid, 2-Methyl-3- (5- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -1 H-pyrrol-3-yl-propionic acid, 2-benzenesulfonylamino-3- (5- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -furan-3-yl) -propionic acid, 2-benzenesulfonylamino-3- [5- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Thiophen-3-yl] -propionic acid, 2-methanesulfonylamino-3- [5- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -1H-pyrrol-3-yl] -propionic acid, 2-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -2-methyl- 1H-pyrrole-3-yl} -propionic acid, 2-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -thiophene-3 -Yl} -propionic acid, and 2- (2,6-Dichloro-benzoylamino) -3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -furan-3-yl} -propionic acid. [39" claim-type="Currently amended] The method of claim 1, A compound which is a compound comprising a moiety of the partial formula 1.1.14: 3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -thiophen-2-yl ] -2-methyl-propionic acid, 2-acetylamino-3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -furan -2-yl] -propionic acid, 2-methanesulfonylamino-3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Thiophen-2-yl] -propionic acid, 2,2-difluoro-3- {5- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- 1H-pyrrole-2-yl} -propionic acid, 2,2-dimethyl-3- [5- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -thiophene-2 -Yl] -propionic acid, 2- (butane-1-sulfonylamino) -3- (5-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -furan-2-yl) -propionic acid, 2-Methyl-3- [5- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -1 H-pyrrol-2-yl] -propionic acid , 2-formylamino-3- {5- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -thiophen-2-yl} -propionic acid, 2-Methyl-3- (5- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -1 H-pyrrol-2-yl) -propionic acid, 2-benzenesulfonylamino-3- (5- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -furan-2-yl) -propionic acid, 2-benzenesulfonylamino-3- [5- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Thiophen-2-yl] -propionic acid, 2-methanesulfonylamino-3- [5- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -1H-pyrrol-2-yl] -propionic acid, 2-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -2-methyl- 1H-pyrrole-2-yl} -propionic acid, 2-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -thiophene-2 -Yl} -propionic acid, and 2- (2,6-Dichloro-benzoylamino) -3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -furan-2-yl} -propionic acid. [40" claim-type="Currently amended] The method of claim 1, A compound which is a compound comprising a moiety of the partial formula 1.1.15: 3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -isoxazol-3-yl ] -2-methyl-propionic acid, 2-acetylamino-3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -isoxo Sazol-3-yl] -propionic acid, 2-methanesulfonylamino-3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) Isoxazol-3-yl] -propionic acid, 2,2-difluoro-3- {5- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Isoxazol-3-yl} -propionic acid, 2,2-dimethyl-3- [5- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -isoxazole-3 -Yl] -propionic acid, 2-allyloxycarbonylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -isolate Sazol-3-yl} -propionic acid, 2- (butane-1-sulfonylamino) -3- (5-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -isoxazol-3-yl) -propionic acid, 2-Methyl-3- [5- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazol-3-yl] -propionic acid, 2-acetylamino-3- {5- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -isothiazol-3-yl} -propionic acid, 2-Methyl-3- (5- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-3-yl) -propionic acid, 2-benzenesulfonylamino-3- (5- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -isoxazol-3-yl) -propionic acid, 2-benzenesulfonylamino-3- [5-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl) -isoxazole- 3-yl] -propionic acid, 2-methanesulfonylamino-3- [5- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -isoxazol-3-yl] -propionic acid, 2-formylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -4-methyl Isoxazol-3-yl} -propionic acid, 2-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -isoxazole- 3-yl} -propionic acid, 3-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -2H-pyrazole -5-yl} -propionic acid, and 2- (2,6-Dichloro-benzoylamino) -3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -isoxazol-3-yl} -propionic acid. [41" claim-type="Currently amended] The method of claim 1, A compound which is a compound comprising a moiety of the partial 3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -oxazol-2-yl ] -2-methyl-propionic acid, 2-acetylamino-3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -oxa Zol-2-yl] -propionic acid, 2-methanesulfonylamino-3- [5- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Oxazol-2-yl] -propionic acid, 2,2-difluoro-3- {5- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Oxazol-2-yl} -propionic acid, 2,2-Dimethyl-3- [5- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -oxazole-2 -Yl] -propionic acid, 2-allyloxycarbonylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl} -methyl] -oxa Zol-2-yl} -propionic acid, 2- (butane-1-sulfonylamino) -3- (5-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -oxazol-2-yl) -propionic acid, 2-Methyl-3- [5- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -oxazol-2-yl] -propionic acid, 2-formylamino-3- {5- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -thiazol-2-yl} -propionic acid, 2-Methyl-3- (5- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -oxazol-2-yl) -propionic acid, 2-benzenesulfonylamino-3- (5- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -oxazol-2-yl) -propionic acid, 2-benzenesulfonylamino-3- [5- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Oxazol-2-yl] -propionic acid, 2-methanesulfonylamino-3- [5- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -oxazol-2-yl] -propionic acid, 2-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- Oxazol-2-yl} -propionic acid, 2-acetylamino-3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -thiazole-2 -Yl} -propionic acid, 2- (2,6-Dichloro-benzoylamino) -3- {5-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -oxazol-2-yl} -propionic acid, and 2-acetylamino-3- [5-({2- [4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -methyl) -1 H-imidazol-2-yl] -propionic acid. [42" claim-type="Currently amended] The method of claim 1, A compound comprising a moiety of the partial formula 1.1.17 and selected from the group consisting of: 3- (5- {1-[(4-benzyloxy-3-methoxy-phenyl) -acetyl] -pyrrolidin-2-yl}-[1,3,4] thiadiazol-2-yl) Propionic acid, 3- [5- (1-{[4- (4-chloro-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl)-[1,3,4] thiadiazol-2-yl ] -Propionic acid, and 3- (5- {1-[(4-benzyloxy-phenyl) -acetyl] -pyrrolidin-2-yl}-[1,3,4] thiadiazol-2-yl) -propionic acid. [43" claim-type="Currently amended] The method of claim 1, Compounds comprising the moieties of the partial formulas 1.1.18, 1.1.19 and 1.1.20 and selected from the group consisting of: 2-acetylamino-3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -phenyl} -propionic acid , 2-formylamino-3- {6- [1-({3-methoxy-4- [3- (3-methyl-pyridin-2-yl) -ureido] -phenyl} -acetyl) -pyrroli Din-2-yl] -pyridin-2-yl} -propionic acid, 3- [4- [1-({3-ethyl-4- [3- (3-methyl-pyridin-2-yl) -ureido] -phenyl} -acetyl) -pyrrolidin-2-yl]- Pyrimidin-2-yl} -propionic acid, 2-acetylamino-3- [3- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl) -phenyl] Propionic acid, 2-acetylamino-3- [3-({2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -methyl) -phenyl] -propionic acid, 2- {2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -pyridin-4-ylmethyl} -4 Methyl-pentanoic acid, 3- {2-[(Methyl-{[4- (3-o-tolyl-ureido) -phenyl] -acetyl} -amino) -methyl] -pyridin-4-yl} -propionic acid, 2-methanesulfonylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl]-[1 , 3,5] triazin-2-yl} -propionic acid, 1- [4- (1-{[6- (3-Pyridin-2-yl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -pyridin-2-ylmethyl ] -Cyclopropanecarboxylic acid, 3- [3- (1-{[6- (3-Pyridin-2-yl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -phenyl] -butyl acid, 2- (butane-1-sulfonylamino) -3- {3-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino)- Methyl] -phenyl} -propionic acid, 2-benzenesulfonylamino-3- [3-({[(2-methoxy-2'-methyl-biphenyl-4-yl) -acetyl] -methyl-amino} -methyl) -phenyl] -propionic acid, 2- (3-{[2- (4-benzyloxy-phenyl) -acetylamino] -methyl} -benzyl) -malonic acid, 2- [3-({2- [4- (4-Chloro-benzyloxy) -phenyl] -acetylamino} -methyl) -benzyl] -malonic acid, 3- [3-({2- [4- (3-Fluoro-benzyloxy) -phenyl] -acetylamino} -methyl) -phenyl] -2- (propane-1-sulfonylamino) -propionic acid, 3- [3-({2- [3-Chloro-4- (4-chloro-benzyloxy) -phenyl] -acetylamino} -methyl) -phenyl] -2- (propane-1-sulfonylamino)- Propionic Acid, 3- (3-{[2- (4-benzyloxy-3-chloro-phenyl) -acetylamino] -methyl} -phenyl) -2- (propane-1-sulfonylamino) -propionic acid, 3- [3-({2- [4- (3-Chloro-benzyloxy) -phenyl] -acetylamino} -methyl) -phenyl] -2- (propane-1-sulfonylamino) -propionic acid, 3- [3-({2- [4- (4-Chloro-benzyloxy) -phenyl] -acetylamino} -methyl) -phenyl] -2- (propane-1-sulfonylamino) -propionic acid, 3- (3-{[2- (4-benzyloxy-3-methoxy-phenyl) -acetylamino] -methyl} -phenyl) -2- (propane-1-sulfonylamino) -propionic acid, 3- (3-{[2- [4- (4-Methyl-benzyloxy) -phenyl] -acetylamino} -methyl) -2-acetylamino-3- (3-{[2- (4-benzyloxy -Phenyl) -acetylamino] -methyl} -phenyl) -propionic acid, 3- (3-{[2- (4-benzyloxy-phenyl) -acetylamino] -methyl} -phenyl) -2- (propane-1-sulfonylamino) -propionic acid, 2- (propane-1-sulfonylamino) -3- {3-[(2-m-tolyl-acetylamino) -methyl] -phenyl} -propionic acid, 3- (3-{[2- (4-hydroxymethyl-phenyl) -acetylamino] -methyl} -phenyl) -2- (propane-1-sulfonylamino) -propionic acid, and 3- [3- (phenylacetylamino-methyl) -phenyl] -2- (propane-1-sulfonylamino) -propionic acid. [44" claim-type="Currently amended] The method of claim 1, A compound comprising a moiety of the partial formula 1.1.21 and a component selected from the group consisting of: 3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -pyrrol-1-yl] 2-methyl-propionic acid, 2-acetylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -pyrrole -1-yl] -propionic acid, 2-methanesulfonylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Pyrrol-1-yl] -propionic acid, 2,2-difluoro-3- {4- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Pyrrole-1-yl} -propionic acid, 2,2-dimethyl-3- [4- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -pyrrole-1- General] -propionic acid, 2- (butane-1-sulfonylamino) -3- (4-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -pyrrol-1-yl) -propionic acid, 2-Methyl-3- [4- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -pyrrole-1-yl] -propionic acid, 2-formylamino-3- {4- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -pyrrole-1-yl} -propionic acid, 2-Methyl-3- (4- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -pyrrole-1-yl) -propionic acid, 2-benzenesulfonylamino-3- (4- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -pyrrole-1-yl) -propionic acid, 2-benzenesulfonylamino-3- [4- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Pyrrole-1-yl] -propionic acid, 2-methanesulfonylamino-3- [4- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -pyrrole-1-yl] -propionic acid, 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- Pyrrole-1-yl} -propionic acid, 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -pyrrole-1- General-propionic acid, and 2- (2,6-Dichloro-benzoylamino) -3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -pyrrol-1-yl} -propionic acid. [45" claim-type="Currently amended] The method of claim 1, A compound comprising a moiety of the partial formula 1.1.22 and selected from the group consisting of: 3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -pyrazol-1-yl ] -2-methyl-propionic acid, 2-acetylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -pyra Zol-1-yl] -propionic acid, 2-methanesulfonylamino-3- [4- (1- {2- [3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetylamino} -3-methyl-butyl) -Pyrazol-1-yl] -propionic acid, 2,2-difluoro-3- [4- [1- (methyl-{[6- (3-o-tolyl-ureido) -pyridin-3-yl] -acetyl} -amino) -ethyl]- Pyrazol-1-yl} -propionic acid, 2,2-Dimethyl-3- [4- (1-{[6- (3-phenyl-ureido) -pyridin-3-yl] -acetyl} -pyrrolidin-2-yl) -pyrazole-1 -Yl] -propionic acid, 2- (butane-1-sulfonylamino) -3- (4-{[methyl-({4- [3- (3-methyl-pyridin-2-yl) -ureido] -piperidine-1- Yl} -acetyl) -amino] -methyl} -pyrazol-1-yl) -propionic acid, 2-Methyl-3- [4- (1-{[4- (2-methyl-benzyloxy) -phenyl] -acetyl} -pyrrolidin-2-yl) -pyrazol-1-yl] -propionic acid, 2-formylamino-3- {4- [1- (biphenyl-4-yl-acetyl) -pyrrolidin-2-yl] -pyrazol-1-yl} -propionic acid, 2-Methyl-3- (4- {1-[(4-o-tolyloxy-phenyl) -acetyl] -pyrrolidin-2-yl} -pyrazol-1-yl) -propionic acid, 2-benzenesulfonylamino-3- (4- {1-[(4-phenoxymethyl-phenyl) -acetyl] -pyrrolidin-2-yl} -pyrazol-1-yl) -propionic acid, 2-benzenesulfonylamino-3- [4- (1-{[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl)- Pyrazol-1-yl] -propionic acid, 2-methanesulfonylamino-3- [4- (3-methyl-1-{[5- (3-o-tolyl-ureido) -pyridin-2-yl] -acetyl} -pyrrolidine-2- Yl) -pyrazol-1-yl] -propionic acid, 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -5-methyl- Pyrazol-1-yl} -propionic acid, 2-acetylamino-3- {4-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -pyrazole-1 -Yl} -propionic acid, and 2- (2,6-Dichloro-benzoylamino) -3- {4-{({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -Methyl] -pyrazol-1-yl} -propionic acid. [46" claim-type="Currently amended] The method of claim 1, A compound comprising a moiety of the partial formula 1.1.23 and selected from the group consisting of: 2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -benzooxazole-6-carboxylic acid, 2- [1- (2- {3-methoxy-4- [3- (3-methyl-pyridin-2-yl) -ureido] -phenyl} -acetylamino) -3-methyl-butyl] -3H -Benzoimidazole-5-carboxylic acid, 2- (1-{[4- (3-pyridin-2-yl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl) -1 H-imidazole [4,5-c] pyridine- 6-carboxylic acid, 2- (1-{[3-Ethoxy-4- (3-pyridin-2-yl-ureido) -phenyl] -acetyl} -pyrrolidin-2-yl) -benzothiazole-6-carboxylic acid, 2-[({[3-methoxy-4- (3-o-tolyl-ureido) -phenyl] -acetyl} -methyl-amino) -methyl] -benzothiazole-6-carboxylic acid, 2-({[(4-benzyloxy-phenyl) -acetyl] -methyl-amino} -methyl) -oxazole [5,4-b] pyridine-5-carboxylic acid, and 3-Methyl-2- {1-[(4-phenoxy-phenyl) -acetyl] -pyrrolidin-2-yl} -3H-benzoimidazole-5-carboxylic acid. [47" claim-type="Currently amended] A compound of formula 1.0.0 as defined in claim 1 and a pharmaceutical for the compound, wherein the amount of the compound is effective for preventing, inhibiting, preventing or reducing cell adhesion and subsequent or associated pathogenic processes after VLA-4 mediated. A pharmaceutical composition comprising a carrier which is suitably acceptable. [48" claim-type="Currently amended] The method of claim 47, A pharmaceutical composition further comprising one or more therapeutic agents. [49" claim-type="Currently amended] 49. The method of claim 48 wherein A pharmaceutical composition, wherein the one or more therapeutic agents are selected from the group consisting essentially of anti-inflammatory corticosteroids, nonsteroidal anti-inflammatory agents, bronchodilators, asthma therapies, immunosuppressants, immune stimulants, anti-metabolic agents, psoriasis therapies, and diabetes therapies. [50" claim-type="Currently amended] The method of claim 49, Therapeutics are theophylline, salbutamol, salmeterol, mometasone, fluticasone, ariflo, montelukast, sulfasalazine, aminosalicylate, cyclosporine, FK-505, rapamycin, clophosphamide, methotrexate and interferon Pharmaceutical composition which is an ingredient selected from the group consisting essentially of. [51" claim-type="Currently amended] Cell adhesion and subsequent mediation by VLA-4, comprising administering to a mammal in need of such treatment a therapeutically effective amount of a compound of Formula 1.0.0 as defined in claim 1 or a pharmaceutical composition according to claim 46; A method of treating or preventing inflammatory, autoimmune, or respiratory diseases by or following the inhibition of pathogenic processes. [52" claim-type="Currently amended] The method of claim 51, wherein Inflammatory, autoimmune or respiratory diseases are essential for asthma, multiple sclerosis, rheumatoid arthritis, osteoarthritis, inflammatory bowel disease, psoriasis, host rejection after organ transplantation, atherosclerosis, and other diseases mediated or associated with VLA-1 A method for treating or preventing inflammatory, autoimmune or respiratory diseases which are diseases selected from the group consisting of: [53" claim-type="Currently amended] A compound converted to the compound of claim 1 in vivo.
类似技术:
公开号 | 公开日 | 专利标题 JP6326057B2|2018-05-16|Substituted pyrimidinyl and pyridinyl-pyrrolopyridinones, methods for their preparation, and their use as kinase inhibitors RU2636050C2|2017-11-20|SUBSTITUTED PYRROLIDINES AS XIa FACTOR INHIBITORS FOR THROMBOEMBOLIC DISEASES TREATMENT RU2660421C2|2018-07-06|Benzylamine derivatives CA2774647C|2017-03-28|Substituted amide compound ES2445714T3|2014-03-04|Polycyclic lysophosphatidic acid receptor antagonists JP4129293B2|2008-08-06|Cell adhesion inhibitor ES2239806T3|2005-10-01|Xa factor inhibitors with a p1 neutral specificity group. ES2246240T3|2006-02-16|Substituted bencimidazols. EP1917262B1|2011-12-14|Piperidine and piperazine derivatives as p2x3 antagonists CA2533594C|2013-04-02|Compounds for inflammation and immune-related uses TWI417096B|2013-12-01|Phenyl and pyridyl compounds for inflammation and immune-related uses EP3224256B1|2019-07-03|N-|arylmethyl)-heteroaryl-carboxamides compounds as plasma kallikrein inhibitors, RU2293727C2|2007-02-20|Anthranilic acid amides with by-side heteroarylsulfonyl chain and pharmaceutical composition containing thereof EP1740581B1|2012-08-22|2, 4, 6-substituted pyridyl derivative compounds useful as beta-secretase inhibitors for the treatment of alzheimer's disease DE69728673T2|2005-03-31|Substituted biphenyl isoxazole sulfonamide KR100862879B1|2008-10-15|N-Substituted hydroxypyrimidinone carboxamide inhibitors of HIV integrase KR101941048B1|2019-01-22|Aminoalkyl-substituted n-thienyl benzamide derivative AU2002326469B2|2006-03-30|Substituted piperazines as modulators of the melanocortin receptor ES2739526T3|2020-01-31|4-hydroxy-3- | pyridin-2-one APJ agonists for use in the treatment of cardiovascular disorders DE60216094T2|2007-06-06|Modulators of peroxisom proliferator activated receptors | ES2264252T3|2006-12-16|Cellular adherence inhibitors mediaated by alfa4. KR101195801B1|2012-11-05|Factor xa inhibitors US5591761A|1997-01-07|Thiophenyl-, furyl-and pyrrolyl-sulfonamides and derivatives thereof that modulate the activity of endothelin DE60127595T2|2008-01-10|Inhibitors of TNF-alpha formation for the treatment of autoimmune diseases AU767456B2|2003-11-13|Biphenyl sulfonamides as dual angiotensin endothelin receptor antagonists
同族专利:
公开号 | 公开日 UY26512A1|2001-07-31| CA2396087A1|2001-07-19| CZ20022072A3|2003-05-14| US20020049236A1|2002-04-25| US20030004196A1|2003-01-02| TNSN00256A1|2002-05-30| US20030100585A1|2003-05-29| AP200202565A0|2002-06-30| ZA200205142B|2003-09-29| PA8509301A1|2002-12-11| PE20010987A1|2001-10-02| CR6682A|2004-01-14| US20040102496A1|2004-05-27| TR200201668T2|2002-11-21| AU2018301A|2001-07-24| OA12126A|2006-05-05| EA004673B1|2004-06-24| YU41202A|2005-03-15| SV2002000246A|2002-07-16| BG106867A|2003-02-28| EE200200372A|2003-12-15| MA26861A1|2004-12-20| IL149758D0|2002-11-10| IS6382A|2002-05-14| SK8692002A3|2003-06-03| NO20023085D0|2002-06-26| WO2001051487A1|2001-07-19| BR0016818A|2002-10-01| AR029216A1|2003-06-18| EA200200619A1|2002-10-31| CO5261616A1|2003-03-31| US6903128B2|2005-06-07| NZ518886A|2004-02-27| HU0203897A2|2003-03-28| CN1413210A|2003-04-23| HU0203897A3|2005-06-28| GT200000226A|2002-06-20| EP1244656A1|2002-10-02| US6667331B2|2003-12-23| JP2003519697A|2003-06-24| PL357109A1|2004-07-12| US6668527B2|2003-12-30| NO20023085L|2002-06-26|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题
法律状态:
1999-12-28|Priority to US17326099P 1999-12-28|Priority to US60/173,260 2000-12-15|Application filed by 화이자 프로덕츠 인코포레이티드 2000-12-15|Priority to PCT/IB2000/001893 2002-08-21|Publication of KR20020067050A
优先权:
[返回顶部]
申请号 | 申请日 | 专利标题 US17326099P| true| 1999-12-28|1999-12-28| US60/173,260|1999-12-28| PCT/IB2000/001893|WO2001051487A1|1999-12-28|2000-12-15|Non-peptidyl inhibitors of vla-4 dependent cell binding useful in treating inflammatory, autoimmune, and respiratory diseases| 相关专利
Sulfonates, polymers, resist compositions and patterning process
Washing machine
Washing machine
Device for fixture finishing and tension adjusting of membrane
Structure for Equipping Band in a Plane Cathode Ray Tube
Process for preparation of 7 alpha-carboxyl 9, 11-epoxy steroids and intermediates useful therein an
国家/地区
|