http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103275157-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/A61K31-7056 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H1-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-056 |
| filingDate | 2013-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2016-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2016-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-103275157-B |
| titleOfInvention | The rupestonic acid amide derivatives containing heterocycle and sugar and preparation method and purposes |
| abstract | The present invention relates to rupestonic acid amide derivatives containing heterocycle and sugar and its production and use; in this analog derivative, the synthesis of the amide derivatives of triazole heterocycle and sugar is first to be obtained the alpine yarrow herb ketoacid derivatives containing end-group alkyne by rupestonic acid and aminopropan alkyne reaction; then obtaining under the catalysis of copper sulfate and sodium ascorbate, in methanol/Feldalat NM, deacetylate obtains target compound further. The method reaction condition is gentle, and experimental procedure is simple and direct. Having the activity of resisiting influenza virus in derivant of the present invention, this compounds can be used for treating influenza as anti-influenza virus medicament. |
| priorityDate | 2013-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 71.