http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6204282-B1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a7f82940e47ba7a1188f8e2ffca55e0f
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D235-14
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D235-10
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D235-14
filingDate 1999-11-29^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2001-03-20^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6cabc765bf3c49b959b63d0a7d996af7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7f2e0b6371d603be0b9099acca7af41c
publicationDate 2001-03-20^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6204282-B1
titleOfInvention Benzimidazole compounds that are vitronectin receptor antagonists
abstract The present invention provides compounds having the formulawherein n, p, q and r are each independently selected from 0 or 1;a, b, c, and d each independently represents a carbon or nitrogen atom, with the proviso that no more than two of a, b, c, and d are nitrogen atoms;Y and Y1 each independently represents 1-4 optional substituents selected from alkyl, alkoxy, halo, -CF3, and -C(O)OH;R1, R2, R3 and R4 are as defined herein;R5, R6, R7, R8, R9, R10, R11 and R12 are independently selected from H or C1-C3 alkyl;and whereinare positioned meta or para relative to each other;or a biolabile ester thereof, or a pharmaceutically acceptable salt thereof. Also provided are methods of using these compounds for treating vitronectin-mediated disorders, e.g., cancer, retinopathy, artherosclerosis, vascular restenosis, and osteoporosis.
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priorityDate 1998-11-30^^<http://www.w3.org/2001/XMLSchema#date>
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