http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102952076-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ac31afbea1cbbb03498644721ffb4a62
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-06
filingDate 2011-08-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7436fab6b04ae1f751e9041eae50e324
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10d89d365026d36e0ca87ebf77d37ad3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aff9ecce90ad72fa12b16e4397bb5a28
publicationDate 2013-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102952076-A
titleOfInvention Preparation of pyrazoline compounds and their application in anticancer therapy
abstract A class of pyrazoline derivatives is characterized in that it has the general formula: In the structural formula, R1 is: pyridyl, 6-chloropyridyl, 6-methylpyridyl, 2-chloro, 6-methyl-pyridyl, 5-bromopyridyl, 2-chloropyridyl. R2 is: 4-methoxy, 4-chloro. R3 is: 4-methoxy, 4-chloro, 4-bromo, 4-fluoro, 4-benzyloxy. R4 is: sulfur atom, oxygen atom. 2. The effect of the pyrazoline derivatives of the present invention on inhibiting the proliferation of MCF7. Therefore, the pyrazoline derivatives of the present invention can be used as potential antitumor drugs. The invention discloses its preparation method.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105949124-A
priorityDate 2011-08-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 21.