http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102516066-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-201 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C59-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00 |
| filingDate | 2011-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2016-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2016-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-102516066-B |
| titleOfInvention | Ostopanic acid analog and Preparation method and use |
| abstract | Do you the present invention relates to ostopanic? acid and analog, the present invention also provides the Preparation method and use of described compound, while utilizing Weinreb acid amides Yu Geshi reagent reacting, selectively rest on the ketone stage, and the characteristic that reaction can not occur builds ostopanic? can two side chains of acid analog, synthesize a series of ostopanic fast? acid analog. Reaction raw materials of the present invention is easy to get, and reaction condition gentleness is simple to operate. The serial ostopanic of synthesized? acid and analog thereof all have significant antitumor action. |
| priorityDate | 2011-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 77.