http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2027778-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D513-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D513-04
filingDate 1990-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_06c011931dea30e0fec509d4a2643ac7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_99109c21d2f3fb7bcd4e9c4b1c9a23b8
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6c07fe5d12053344b689cd02b90dd316
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3619dfbb918e468ae3bed6fba88f2b86
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d80a64963ee8fe9b74b312485d70a24d
publicationDate 1992-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2027778-A1
titleOfInvention Optically active thiazetoquinoline-3-carboxylic acid compound, method for preparation thereof, and a pharmaceutical composition comprising the same
abstract ABSTRACT: An optically active thiazetoquinoline-3-carboxylic acid compound represented by the following formula (I): (I) wherein R1 is a hydrogen atom or a lower alkyl group; R2 is a fluorine atom or a chlorine atom; R3 is a hydrogen atom, a lower alkanoyl group, a halogenated lower alkanoyl, or the residue of carboxylic acid ester; and C * represents an asymmetric carbon atom of S- or R-configuration, a pharmacologically acceptable salt thereof, and a method for preparing the compound are disclosed. ALSO disclosed are antibacterial agent, antineoplastic agent, and anti-AIDS virus agent comprising the same, a pharmaceutical composition for the treatment of bacterial infectious disease, tumor, and AIDS comprising an effective amount of the same.
priorityDate 1990-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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