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filingDate 2002-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2005-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_54616c6d9fff4a1e96a0f504f118d7b1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_549f7bcb786f4f1bb2e0d74ad552ad6f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1e95361a110a5ad79175399585459daa
publicationDate 2005-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6855843-B2
titleOfInvention Inhibitors of α4 mediated cell adhesion
abstract The present invention relates to a pharmaceutical composition comprising as an active ingredient a compound of formula (I), wherein Ring A is an aromatic or a heterocyclic ring; Q is a bond, carbonyl, lower alkylene, lower alkenylene, —O— -(lower alkylene)-, etc.; n is 0, 1 or 2; Z is oxygen or sulfur; W is oxygen, sulfur, —CH═CH—, —NH— or —N═CH—; R 1 , R 2 and R 3 are the same or different and are hydrogen, halogen, hydroxyl, a substituted or unsubstituted lower alkyl gorup, a substituted or unsubstituted lower alkoxy group, a substituted or unsubstituted amino group, etc.; R 4 is tetrazolyl, carboxyl group, amide or ester; R 5 is hydrogen, nitro, amino, hydroxyl, lower alkanoyl, lower alkyl, etc.; R 6 is selected from (a) a substituted or unsubstituted phenyl group, (b) a substituted or unsubstituted pyridyl group, (c) a substituted or unsubstituted thienyl group, (d) a substituted or unsubstituted benzofuranyl group, etc.; or a pharmaceutically acceptable salt thereof.
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priorityDate 1998-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 2767.