http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101766874-B1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C49-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C49-82 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C49-84 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C49-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-61 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-61 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-84 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-76 |
| filingDate | 2015-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2017-08-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2017-08-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-101766874-B1 |
| titleOfInvention | Synthetic methods for prenylated chalcones and pyranochalcones |
| abstract | The present inventors have invented a simple and effective method for synthesizing natural prenyl chalcone and pyran chalcone compound 1-9 using Claisen-Schmidt condensation as a main step. In addition, the anti-inflammatory effects of the synthesized compounds were evaluated in RAW 264.7 macrophages stimulated with glutathione peroxidase. As a result, chalcone compounds having a phenyl group at the ring A (acetophenone portion) did not exhibit a weak inhibition or inhibition against nitric oxide production, whereas chalcone (5, 6, 8 and 9) Showed normal or good activity, and no cytotoxicity. |
| priorityDate | 2015-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 332.