http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2011126544-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-02
filingDate 2011-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0e4ca22113b0df9297adac1cfdd675b1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2163a1e6b26f709864ead2764ff5749f
publicationDate 2011-10-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2011126544-A2
titleOfInvention Thymoquinone analogs for the treatment of pancreatic cancer
abstract Analogs of thymoquinone, an active compound extracted from Nigella n sativa (black seed oil) are 2,5-bis (alkyl/aryl amino) 1, 4-benzoquinones, are more potent than the naturally-occurring compound (e.g, have a lower IC 50 ) in terms of inhibition of cell growth, induction of apoptosis, and modulation of transcription fact NF-ĸB. Used in conjunction with conventional chemotherapeutic agents, such as gemcitibine or oxaliplatin, the analogs sensitize gemcitabine-resistant pancreatic cancer cells to gemcitabine-induced apoptosis. A preferred compound is 2,5-dichloro- 3,6-bis[3-methoxyphenyl)amino]cyclohexa-2,5,-diene- 1,4-dione.
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