http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CS-218583-B2
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2ca2e4410855da087e11bf3eea8933fa |
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 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-44 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 |
Incoming Links
Total number of triples: 48.