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filingDate 2017-04-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_52317fed040bae1707d618b06c92cc33
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publicationDate 2017-08-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-107041888-A
titleOfInvention A kind of chloro-salicylic aldehyde of cancer therapy drug 5 contracting hydrazino pyridine schiff bases cobalt complex of 2 bromine 6 and synthetic method
abstract A kind of chloro-salicylic aldehyde of cancer therapy drug 5 contracting 2 bromine 6 hydrazino pyridine schiff bases cobalt complex [Co (bhcp) 2 ] 2 And synthetic method.The cobalt complex [Co (bhcp) 2 ] 2 Molecular formula be:2(C 24 H 16 Br 2 Cl 2 CoN 6 O 2 ), molecular weight is:1420.15g/mol, Hbhcp are the 5 chloro-salicylic aldehydes contracting hydrazino pyridine schiff bases of 2 bromine 6.By analytically pure 5 chloro-salicylic aldehydes of 1.565g, the analytically pure hydrazino pyridines of 2 bromine 6 of 1.880g are dissolved in 30mL analysis straight alcohol solution, part Hbhcp are obtained after being heated to reflux two hours.Dried 0.157 0.314g Hbhcp are dissolved in 5 10mL and analyze pure DMF, 0.145 0.291g analyzes pure cabaltous nitrate hexahydrate and is dissolved in 5 10mL analysis straight alcohols, it is placed in reactor, three days is stood in 80 DEG C of baking ovens, has red bar crystal to generate i.e. [Co (bhcp) 2 ] 2 。[Co(bhcp) 2 ] 2 There is certain inhibition to JEG-3, but cis-platinum is far below to toxicity to the normal liver cells of HL 7702 strain cell, be a kind of inorganic cancer therapy drug.Present invention process is simple, with low cost, chemical constituent is easily controllable, reproducible and yield is high.
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