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filingDate 1998-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a2fdb9e660a44fd88bf99904ba8d0644
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2cc292410a4b8a5912d6ae8e0ae29bbd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_351266bb714df09224a7007992c9998a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6704020203373ae815bf1a29eb16388f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fb90c3e9ed86a442f4103967b43ee34c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_65454f73395f925eeca98f077f96c8d5
publicationDate 2002-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber NZ-502813-A
titleOfInvention N-aroylphenylalanine derivatives as inhibitors of the interaction between a4 containing integrins and VCAM-1
abstract Described are compounds of formula (I), wherein One of X and X' is hydrogen, halogen, or C1-6 alkyl, the other is a group of formula (II), or one of X and X' is a group of formula (III), wherein Het is a 5- or 6-membered heteroaromatic ring or Het is a 9- or 10-membered bicyclic heteroaromatic ring, or one of X and X' is a group of formula (IV), and Y is a group of formula (V), or a group selected from a 5- or 6-membered monocyclic heteroaromatic group containing 1-3 heteroatoms selected from N, O, and S or a 10-membered bicyclic heteroaromatic group containing 1-4 heteroatoms, selected from N, O, and S, wherein the heteroaromatic group is bonded via a carbon atom to the amide carbonyl, and Z is hydrogen or C1-6 alkyl. The compounds are used as medicaments for treating rheumatoid arthritis, multiple sclerosis, inflammatory bowel disease and asthma.
priorityDate 1997-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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