http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H10130147-A

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filingDate 1997-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fd8816afd8b61a495c1463a2d52d1261
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_03cf1ccd9f76a99234b7d4759952faef
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b2c34b9cc58fb2c2fd96d4a7913f4069
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1dd6d2792f4367d10d2d0c5b534a821b
publicationDate 1998-05-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H10130147-A
titleOfInvention Pharmaceutical composition containing heterocyclic substituted acylaminothiazole
abstract (57) Abstract: The present invention relates to a cholecystokinin (CCK) antagonist comprising a 2-acylaminothiazole compound as an active ingredient. SOLUTION: Formula: embedded image Wherein R 1 and R 2 represent H or alkyl; R 3 is an optionally substituted cycloalkyl or an optionally substituted aromatic group, and represents phenyl or a heterocyclic ring containing one or more hetero atoms selected from O, S and N; R 2 and R 3 together The carbon of the optionally substituted phenyl may be attached at the 4-position of the thiazolyl ring, and Z comprises one or more heteroatoms selected from O, S and optionally substituted N. And a substituted or unsubstituted heterocyclic ring], and an addition salt of an acid or base of these compounds as an active ingredient, a cholecystokinin (CCK) antagonist.
priorityDate 1989-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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