http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0649843-B1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_44c713790ce00813da2e6c6d57a29456
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P7-02
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12
filingDate 1993-07-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2000-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f4c8641064041368ce26977d912ff8e5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2e2d1c4136631fafca72b2b3e4a3e604
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cd8323cfd948e2deb97355551cfaeae4
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0c4c0fc12e99ac3d889811d8fc3be38f
publicationDate 2000-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0649843-B1
titleOfInvention Thiazoline derivative
abstract To provide a compound excellent in fibrinogen receptor antagonism and cell adhesion factor antagonism. A thiazoline derivative represented by general formula (I) and a salt thereof, wherein R<1> represents cyano, carbamoyl, thiocarbamoyl, morpholinothiocarbonyl, alkylthioimidoyl, -C(=NH)-NR<1><1>R<1><2> (wherein R<1><1> and R<1><2> represent each hydrogen, alkyl, alkoxycarbonyl, cycloalkyl, phenyl, substituted phenyl, aralkyl or substituted aralkyl, or alternatively R<1><1> and R<1><2> may be combined with each other to represent a monovalent heterocyclic group together with the adjacent nitrogen atom) or imidazolin-2-yl; R<2> represents alkyl or aralkyl; R<3> represents carboxy, hydroxy, alkoxycarbonyl, benzyloxycarbonyl or pyridyl-methyloxycarbonyl; and n represents an integer of 1 to 3. <CHEM>
priorityDate 1992-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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