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filingDate 2009-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bda4c147c6c8f036c9df0a507e570e03
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5e65f050bd77e37a07d5e2fb63de2a21
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_380d91885df6dd7144f70ff6c88fa624
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1d42b5d86f657c98b16884efa8a21a8a
publicationDate 2013-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102093320-B
titleOfInvention Soluble epoxide hydrolase inhibitor
abstract The invention provides a soluble epoxide hydrolase inhibitor, which has the following structural formula I, wherein R1 is N-R2R3; R2 and R3 are hydrogen, C1-C4 alkyl, aromatic ring, aromatic heterocyclic ring, or C1-C4 alkyl connected with the aromatic ring or the aromatic heterocyclic ring respectively; and the R2 can also be connected with the R3 to form a ring, then R1 is a quinary, hexahydric or heptabasic heterocyclic ring containing 1 nitrogen atom or 1 oxygen atom, and the nitrogen atom can be directly connected with the hydrogen and can also be connected with the C1-C4 alkyl. Rat experiment group results in an anesthesia state and a non-anesthesia state show that the inhibitor has certain blood pressure reducing effect, can be used for preparing medicaments for preventing and treating cardiovascular diseases, and has broad clinical application prospect. The invention provides a preparation method.
priorityDate 2009-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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