http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6032793-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-35
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-00
filingDate 1983-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_63b4ce533409c2e6729629c418ee8220
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6300a72a477b9b2ee1c53f63d1fb84ab
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publicationDate 1985-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6032793-A
titleOfInvention Novel bruceolide derivative and its preparation
abstract NEW MATERIAL:A compound shown by the formula I (R 1 is H, t-butyldimethylsilyl, methoxyethoxymethyl, or methoxymethyl; R 2 is β-methyl-α,β-unsaturated fatty acid residue having 5W18C main chain, or 1W18C straight-chain alkylcarbamic acid residue). n EXAMPLE: 3-o-t-Butyldimethylsilyl-15-o-3'-methyl-2'-octenoyl bruceolide. n USE: A carcinostatic agent. Having low toxicity. n PREPARATION: For example, a hydroxyl group at 15-position of a bruceolide derivative shown by the formula II (R 3 is t-butylmethylsilyl, methoxyethoxymethyl, or methoxymethyl) is esterified with a β-methyl-α,β-unsaturated fatty acid having 5W18C main chain, or 1W18C straight-chain alkyl isocyanate is added to the derivative, to give a compound shown by the formula I (with the proviso that group R 1 is R 3 ). n COPYRIGHT: (C)1985,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-02062334-A3
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priorityDate 1983-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 25.