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filingDate 2001-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_89d9565ba3c3094a6d794bc82900a336
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publicationDate 2005-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1346982-A4
titleOfInvention INHIBITORS OF VLA-4
abstract Compounds represented by the general formula (I) or salts thereof, and medicines containing the same: (I) [wherein W is WA-A1-WB- (wherein WA is optionally substituted aryl or the like; A?1 is -NR1¿-, a single bond, -C(O)-, or the like; and WB is optionally substituted arylene or the like); R is a single bond, -NH-, -OCH¿2?-, alkenylene, or the like; X is -C(O)-, -CH2-, or the like; and M is, e.g., a group represented by the general formula (iii): (iii) (wherein R?11, R12, and R13¿ are each independently hydrogen, hydroxyl, amino, halogeno, or the like; R14 is hydrogen or lower alkyl; Y is -CH¿2?-O- or the like; Z is optionally substituted arylene or the like; A?2¿ is a single bond or the like; and R10is hydroxyl or lower alkoxy)]. The compounds or the salts selectively inhibit the binding of cell adhesion molecules to VLA-4 and exhibit high oral absorbability, thus being useful as preventive and/or therapeutic drugs for inflammatory diseases, autoimmune diseases, cancerous metastasis, bronchial asthma, nasal occlusion, diabetes, and so on.
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Total number of triples: 66.