http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2016523934-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-13 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J15-005 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K36-068 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-575 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J9-00 |
| filingDate | 2014-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2016-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2016523934-A |
| titleOfInvention | Ergosterol compounds and methods for producing and using the same |
| abstract | The present invention provides an ergosterol compound, a method for producing the same, and a use thereof. The ergosterol compound has a molecular formula of C 28 H 44 O, a molecular weight of 396.34, and a molecular structure of (3R, 9R, 10S, 13S, 14S, 17S) -17-((2S, 5R, E) -5. , 6-Dimethylhept-3-en-2-yl) -10,13-dimethyl-2,3,4,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopentadiene [Α] phenanthrene-3-ol), which is a completely new chemical structure. The source of this molecule is sanagitake, and this compound and its crystals are obtained by crushing, extracting, concentrating, separating and crystallizing sanagitake fruit bodies, have a highly effective antitumor action, and are completely new. Structure and potential to develop new antitumor drugs. |
| priorityDate | 2014-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 53.