http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6259258-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1374dd16777534b65ad4422333245af8
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C405-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C401-00
filingDate 1985-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0c78d50133246ed8b24f359ce49c9f0c
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publicationDate 1987-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6259258-A
titleOfInvention Punaglandin compound and production thereof
abstract NEW MATERIAL:The compound of formula I (R 1 is 1W10C alkyl; R 2 is OH- protecting group or H; A is H and B is OH or A and B together form a bond; *represents optically active or inactive C atom). n USE: A carcinostatic agent and antiviral agent. It exhibits strong proliferation- inhibiting activity against L1210 leukemia cell and has proliferation-inhibiting action also against herpes simplex virus. n PREPARATION: The compound of formula I can be produced by the aldol conden sation reaction of the cyclopentenone compound of formula II (R 20 is OH- protecting group) with the aldehyde of formula III in the presence of lithium diisopropylamide in a solvent such as ether at -100W+50°C. n COPYRIGHT: (C)1987,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9825593-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1704855-A3
priorityDate 1985-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 23.