http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102134210-B
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b4711b7defc1422cdb7f86d2c95657bf |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C323-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C323-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C319-20 |
filingDate | 2010-01-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2014-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fac2691859523b797ad3422aa985bc77 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_128ebf3696b16017036e5e0b9c0d2180 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6ac5c8bfbf120c217f8f45b5efb8d655 |
publicationDate | 2014-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CN-102134210-B |
titleOfInvention | Leonurine derivative and preparation method thereof |
abstract | The invention belongs to the field of medicament synthesis, in particular relating to a derivative obtained by combining leonurine with an L-cysteine analogue and a synthesis method thereof. The preparation method comprises the following steps: on the basis of utilizing syringic acid as a starting raw material, successively carrying out carbonylation reaction, esterification reaction, ester hydrolysis reaction and the like, so as to synthesize the derivative obtained by combining the leonurine with the L-cysteine analogue. The method is strong in operability and easy to control, the reaction condition is simple, the yield and purity of the product are high, the derivative obtained by combining the leonurine with the L-cysteine analogue can be used as a novel candidate medicament released by endogenous hydrothion. |
priorityDate | 2010-01-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 43.