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filingDate 2001-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a8b491adf6e1bbaa3e5bf3cedb89f1b3
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publicationDate 2002-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PE-20020665-A1
titleOfInvention CYCLOALKYL PHENYL ALCANOIC ACID AS ANTAGONIST OF INTEGRINS OVß3
abstract REFERS TO FORMULA I CYCLOALKYL PHENYL ALCANOIC ACID COMPOUNDS WHERE RING A IS A 4-8 MEMBER MONO-CYCLE RING, 7-12-MEMBER BICYCLE RING; A1 IS A 5-9 MEMBER MONOCYCLE RING, 7-14 MEMBER POLYCYCLE HETERO CYCLE, NR5-C (= Y1) -NR8R7, NR5C (Y2) (= NR7); WHEN Z1 IS CO, SO2, THE A1-Z2 LINK INCLUDES PYRIDINE, IMIDAZOLE, THIAZOLE, OXAZOLE, BENZIMIDAZOLE, IMIDAZOPYRIDINE; Y1 IS NR2, O, S; R2 IS H, ALKYL, ARYL, OH, ALCOXY; R7 AND R8 ARE H, ALKYL, ARALKYL, AMINO, ALKYLAMINE; NR7 AND R8 FORM A SINGLE CYCLE, BICYCLE RING; R5, Rm, Rp, Rk, Rf ARE H, ALKYL; A IS NR5C (Y) = NR '; Y2 IS RENT, CYCLOALKYL, CYCLOALKYL, BETWEEN GOLD; Z1 IS CH2, O, NH, NRk, AMONG OTHERS; Z2 IS A C2-C5 LINK; Z1-Z2 ALSO CONTAINS CARBOXAMIDE, SULFONE, LINKED TO RING A IN POSITION FOR OR TARGET IN RELATION TO X1; n IS 0-1; Rc IS H, ALKYL, HALOGEN, OH, AMONG OTHERS; X1 IS O, CO, SO2, NRm, (CHRp) q; Rp IS H, ALKYL, ALCOXY, OH; q IS 0-1; X2 IS CHRe, CO, SO2, NRf, S. X or Y IS CRg, N; Rg IS H, ALKYL, HALOALKYL, FLUORINE, AMONG OTHERS, X-X2-Y CONTAINS ACILO, ALKYL, AMINO, AMONG OTHERS; Rb ES X3-Rh; X3 IS O, S, NRj; Rj AND Rh SON H, RENT, ACILO, AMONG OTHERS. THE PREFERRED COMPOUNDS ARE 2- [4- [3- (2-PYRIDINYLAMINE) PROPOXI] PHENYL] CYCLOPROPANE-ACETIC ACID, AMONG OTHERS. THE COMPOUNDS ARE ANTAGONISTS OF INTEGRIN OVß3 AND MAY BE USEFUL FOR THE TREATMENT OF TUMOR METASTASIS, TUMOR GROWTH, OSTEOPOROSIS, PAGET'S DISEASE, RETINOPATHY, MACULAR DEGENERATION
priorityDate 2000-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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