http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107417532-B
Outgoing Links
Predicate | Object |
---|---|
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C219-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D317-64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C69-736 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-736 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C219-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-64 |
filingDate | 2017-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2020-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2020-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CN-107417532-B |
titleOfInvention | Resveratrol acrylic acid phenolic ester derivative and preparation method and application thereof |
abstract | The invention discloses a resveratrol acrylic acid phenol ester derivative and a preparation method and application thereof, wherein the structure of the resveratrol acrylic acid phenol ester derivative is as follows: the result of biological activity tests shows that the resveratrol acrylic acid phenolic ester derivative can inhibit L PS stimulated RAW264.7 from releasing NO, and has NO cytotoxicity in an effective anti-inflammatory concentration range. |
priorityDate | 2017-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 98.