http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103961340-B
Outgoing Links
Predicate | Object |
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classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-65 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-122 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-83 |
filingDate | 2014-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2019-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2019-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CN-103961340-B |
titleOfInvention | A kind of LSD1 inhibitor and its application |
abstract | The present invention relates to novel LSD1 inhibitor and the applications in drug, are especially preparing anti-LSD1 inhibitor medicaments and are treating the application in the drugs such as tumour, virus infection, blood disease, the chemical structural formula of the LSD1 inhibitor is as follows: Compound I: 2 carbon of phenyl ring therein are connected with bromine atom, and 4,5,3 ', 4 ' position carbon are connected with hydroxyl.Chemical name Chinese are as follows: (3 ', 4 '-dihydroxy-phenyl)-(bromo- 4, the 5- dihydroxy-phenyl of 2-)-ketone;English are as follows: (3 ', 4 '-dihydroxyphenyl)-(2-bromo-4,5-dihydroxyphenyl) methanone.Compound II: 2,2 ' position carbon of phenyl ring therein is connected with bromine atom, and 4,5,4 ', 5 ' position carbon are connected with hydroxyl.Chemical name Chinese are as follows: (2 '-bromo- 4 ', 5 '-dihydroxy phenyl)-(bromo- 4, the 5- dihydroxy phenyl of 2-)-ketone;English are as follows: (2 '-bromo-4 ', 5 '-dihydroxyphenyl)-(2-bromo-4,5-dihydroxyphenyl) methanone. |
priorityDate | 2014-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 54.