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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-395
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D225-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
filingDate 1979-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5bff6d3207f63b0b3f5765ea958fb19b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0cf9d96bab23f219c0f12c7bdea2640c
publicationDate 1980-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S55111470-A
titleOfInvention Geldanamycin derivative, its preparation, antitumor drug comprising it as active ingredient
abstract NEW MATERIAL:A geldamycin derivative shown by formula I (R 1 is methoxy or di lower alkyl amino; R 2 is di lower alkyl amino). n EXAMPLE: 17-Dimethoxy-17,19-bisdimethylamino-geldanamycin. n USE: A synthetic intermediate for an antitumor agent, a drug for a veterinarian, or other derivative. a daily dose for an adult is 0.5W80mg/kg in the case of nonoral administration and 1W100mg/kg in the case of oral administration. n PROCESS: A geldanamycin shown by the formula II is reacted with a di lower alkylamine, e.g., dimethylamine, preferably in an organic solvent, e.g., a mixed solvent of chloroform and methanol at room temperature to give the desired compound shown by the formula I. The di lower alkylamine can also be used in the form of an aqueous solution. n COPYRIGHT: (C)1980,JPO&Japio
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priorityDate 1979-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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