http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-593293-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cac023d2e2874224ecbbcccbdea1fc91
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-426
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-34
filingDate 2000-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2004-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_98ae596938141f42b0513b60bf49dc3d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_96dd2bdb60874f485541ef3e57d49421
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_33d8bca1d5eaf0f63c2626c4b6e3609d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_78db76a48395c38d4a80d1fbf0af6d94
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6d6253bbe71a9c2014c4a6bf2da31b6e
publicationDate 2004-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-593293-B
titleOfInvention Substituted benzylthiazolidine-2,4-dione derivatives
abstract Substituted benzylthiazolidine-2, 4-dione derivatives of the formula (I), [wherein the bond form of A is -CH2CONH-, -NHCONH-, -CH2CH2CO- and -NHCOCH2-, B is a C1-4 lower alkyl group, a C1-3 lower alkoxy group, a halogen atom, trifluoromethyl group, trifluoromethoxy group, an optionally substituted phenyl group, an optionally substituted phenoxy group or an optionally substituted benzyloxy group], or the pharmaceutically acceptable salts and the hydrates thereof, and the process for the preparation thereof are disclosed. These compounds can bond with the receptor as the ligand of PPAR to activate and have the blood sugar reducing effect and lipid reducing effect.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-I461423-B
priorityDate 1999-08-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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