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filingDate 1996-07-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f0157651969d177c83ff7c7bb6db4702
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_86ea376a522fda49d7876b0f3610fbde
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9fb7aac78fb5962b9df151b36b669b0b
publicationDate 1998-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CZ-2598-A3
titleOfInvention Platelet aggregation inhibitors
abstract Compounds of formula (I), wherein B is O or CH2; X is selected from NR<1>R<2>, SR<1>, and C1-C7 alkyl; Y is selected from SR<1>NR<1>R<2>, and C1-C7 alkyl; R<1> and R<2> are each and independently selected from H, or C1-C7 alkyl optionally substituted upon or within the alkyl chain by one or more of O, S, N or halogen; R<3> and R<4> are both H, <u>or</u> R<3> and R<4> together form a bond; A is COOH, C(O)NH(CH2)pCOOH, C(O)N[(CH2)qCOOH]2; C(O)NHCH(COOH)(CH2)rCOOH, <u>or</u> 5-tetrazolyl, wherein p, q and r are each and independently 1, 2, or 3; as well as pharmaceutically acceptable salts and prodrugs thereof, pharmaceutical compositions comprising the novel compounds and use of the compounds in therapy. Also within the scope of the invention are novel intermediates to the novel compounds. The novel compounds are in particular useful in the prevention of platelet aggregation.
priorityDate 1995-07-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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