http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102453036-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-90 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P13-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P3-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P7-04 |
| filingDate | 2010-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2015-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2015-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-102453036-B |
| titleOfInvention | A kind of camptothecin compound and its preparation method and application in pesticide |
| abstract | The present invention relates to a new class of camptothecin compounds, as well as the preparation method and application of this compound in pesticides. The preparation method of the compound is that <i>N</i>-(1ˊ-oxyl-2ˊ,2ˊ,5ˊ,5ˊ-tetramethylpyrrole-amide)-3ˊ-<i>L</i>-amino acid React with 5-hydroxyethyl oxycamptothecin under the action of an appropriate amount of catalyst and dehydrating agent, and obtain it after purification and separation. Through the insecticidal, bacteriostatic and herbicidal activity tests of this type of compound, it is proved that this type of compound has better poisonous activity against agricultural pests (such as cocoa beetle and Spodoptera litura) than camptothecin and DRF-1042. Bacteria (such as mango anthracnose and mango stalk rot) and farmland weeds (such as crabgrass, mustard and amaranth) have a better inhibitory effect. |
| priorityDate | 2010-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 45.