http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106632375-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A23V2002-00 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D493-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-35 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P3-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A23L33-105 |
| filingDate | 2016-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2018-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2018-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-106632375-B |
| titleOfInvention | A kind of flavone compound for being isolated from pueraria lobata and its preparation method and application |
| abstract | The invention discloses a kind of flavone compound 2 ', 3 epoxies 4,4,4 ', 7 tetrahydroxy, 5 ' geranyl flavane and its preparation method and application, the compound is by the way that, successively using ethyl acetate, extracting n-butyl alcohol, n-butyl alcohol extract is with chloroform after high concentration ethanol refluxing extraction：Methanol is as eluant, eluent through silica gel column chromatography, carry out preparative liquid chromatography separating step again and obtain, gained compound not only has stronger α glucosidase inhibitory actives, and the suppression type to glycosidase is irreversible inhibition, be expected to be developed in the future for it is safely and effectively hypoglycemic, adjust feeding desorder, treatment is overweight or the medicine of the nutritive disease such as fat. |
| priorityDate | 2016-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 73.