http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1009401-A1

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7a90597b8e0527c4b450235322359da2
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D495-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-407
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P17-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-407
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D495-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
filingDate 1998-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0c1cbf155f4c82c5cbfb1d43654a52b6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_307a08babe4d0b530951692a9e07b393
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_69884dd85f3ee479f604712d1a4164e7
publicationDate 2000-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1009401-A1
titleOfInvention Dithiolopyrrolones and their corresponding monoxides and dioxides as antineoplastic agents
abstract Compounds, isolated from the bacteria Xenorhabdus bovienii, having formula (1), wherein R1 = hydrogen, substituted or unsubstituted alkyl, cycloalkyl, aryl, aralkyl, or heterocyclyl group; R2 = hydrogen, substituted or unsubstituted alkyl, cycloalkyl, aryl, aralkyl, heterocyclyl or group acyl; R3 = hydrogen, alkyl, cycloalkyl, aralkyl, aryl or heterocyclyl group, or (2), wherein R1 = hydrogen, substituted or unsubstituted alkyl, cycloalkyl, aryl, aralkyl, or heterocyclyl group; R2 = hydrogen, substituted or unsubstituted alkyl, cycloalkyl, aryl, aralkyl, heterocyclyl or group acyl; R3 = hydrogen, alkyl, cycloalkyl, aralkyl, aryl or heterocyclyl group, or (3), wherein R1 = hydrogen, substituted or unsubstituted alkyl, cycloalkyl, aryl, aralkyl, or heterocyclyl group; R2 = hydrogen, substituted or unsubstituted alkyl, cycloalkyl, aryl, aralkyl, heterocyclyl or group acyl; R3 = hydrogen, alkyl, cycloalkyl, aralkyl, aryl or heterocyclyl group or the salts thereof have antineoplastic activity. The invention provides pharmaceutical compositions containing the compounds and the methods for employing them as medicaments, particularly in the treatment of human and animal cancers.
priorityDate 1997-09-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID595
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426157139
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9AXH0
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226393712
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226401011
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ6G9M4
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID25271757
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9X576
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID16682730
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP19515
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226394161
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP07145
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ97FE0

Total number of triples: 319.