http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102432639-B

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-415
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F17-02
filingDate 2011-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-11-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_465d2b410593b8510db50a283c31a08f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8dd683fe7a37129fab8ad027f9fdaaed
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publicationDate 2013-11-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102432639-B
titleOfInvention 1-(2-hydroxy-3-(phenylamino)propyl)-3-ferrocenyl-1H-pyrazole-5-ethyl formate compound and medicinal use thereof
abstract The invention discloses a 1-(2-hydroxy-3-(phenylamino)propyl)-3-ferrocenyl-1H-pyrazole-5-ethyl formate compound and a medicinal use thereof. The 1-(2-hydroxy-3-(phenylamino)propyl)-3-ferrocenyl-1H-pyrazole-5-ethyl formate compound is a chiral 1-(2-hydroxy-3-(phenylamino)propyl)-3-ferrocenyl-1H-pyrazole-5-ethyl formate derivative. A result of a pharmacological experiment shows that the 1-(2-hydroxy-3-(phenylamino)propyl)-3-ferrocenyl-1H-pyrazole-5-ethyl formate compound has an obvious effect of inhibiting lung cancer cell proliferation; and lung cancer cell A549 inhibition activity of the 1-(2-hydroxy-3-(phenylamino)propyl)-3-ferrocenyl-1H-pyrazole-5-ethyl formate compound is superior to lung cancer cell H322 inhibition activity of the 1-(2-hydroxy-3-(phenylamino)propyl)-3-ferrocenyl-1H-pyrazole-5-ethyl formate compound. Therefore, the 1-(2-hydroxy-3-(phenylamino)propyl)-3-ferrocenyl-1H-pyrazole-5-ethyl formate compound as a novel ferrocenyl group-containing chiral pyrazole derivative has clinical application development prospects and has important meaning to antitumor drug development.
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type http://data.epo.org/linked-data/def/patent/Publication

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