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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D519-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-475
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D519-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
filingDate 1979-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_be99737868c87a8a25a377ec0c45fb84
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_16688af6909dfce86a9b1c3b7d7158a6
publicationDate 1983-02-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CS-218583-B2
titleOfInvention Method of making the c3-carboxhydrazides 4-deacetylvinkaleukoblastine
abstract 4-Desacetyl vincaleucoblastine C-3 carboxhydrazides of the formula …<CHEM>… wherein Q is …<CHEM>… R is, when taken singly, C1-C3 alkyl, beta -hydroxyethyl, beta -acetoxyethyl, C2-C4 alkanoyl, dichloroacetyl, benzoyl or C1-C3 alkyl carbazyl;… R<1> is, when taken singly, methyl or H only when R is C1-C3 alkyl and is H otherwise; and… R and R<1>, when taken together, form a C1-C3 alkylidene group. …<??>The compounds are prepared by reacting the C-3 carboxazides with …<CHEM>… or by reacting the unsubstituted C-3 carboxhydrazide with acetone or with the appropriate aldehyde, acid anhydride or acid chloride. …<??>The compounds are useful in inhibiting the growth of tumors.
priorityDate 1978-04-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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