http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S63243079-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-48
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filingDate 1987-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_df0e2469cba8cd7b223110d2836a5851
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b43a32ebb0beff5911f5b8387f7bc7d9
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publicationDate 1988-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S63243079-A
titleOfInvention Thiazole derivative
abstract NEW MATERIAL:The compound of formula I (M is 5W7-membered heterocyclic base containing two N atoms.; A is substituent group on one of the N atoms. of the group M and is H, aryl, aralkyl, heteroaryl, heteroaralkyl or cycloalkyl; M is a group bonded to the other N atom. of the group M and is single bond or lower alkylene; B is group of formula II; R 1 is amino, hydrazino, guanidino, isothioureido or thioureido) and its salt. n EXAMPLE: 1-( 4-Fluorophenyl )-4-( 2-guanidino-1,3-thiazol-4-yl )methylpiperazinehy drochloride. n USE: It has excellent Gasping prolonging action and antagonistic action against lethal hypoxia. It is non-toxic and is useful as a cerebral function improver. n PREPARATION: The compound of formula can be produced e.g. by reacting an amino compound of formula A-M-H with a compound of formula III (X is halogen, alkanesulfonyloxy, etc.). n COPYRIGHT: (C)1988,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5925635-A
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priorityDate 1987-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457444288

Total number of triples: 29.