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Bioorg Med Chem Lett ; 20(6): 1961-4, 2010 Mar 15.
Article in English | MEDLINE | ID: mdl-20171096

ABSTRACT

A kind of racemic furan lignans were synthesized via a novel route, and two optical isomers were obtained through a selective hydrolization. The absolute configurations were determined by circular dichroism spectroscopy after separated through a preparative column. The different activities of isomers and the racemates were evaluated on QGY-7701 and HeLa cell lines, and compound 2c showed the best activity on QGY-7701 and HeLa cell lines with IC(50) 12 microM and 13 microM, respectively.


Subject(s)
Antineoplastic Agents/chemical synthesis , Antineoplastic Agents/pharmacology , Furans/chemical synthesis , Furans/pharmacology , Lignans/chemical synthesis , Lignans/pharmacology , Antineoplastic Agents/chemistry , Chromatography, High Pressure Liquid , Drug Screening Assays, Antitumor , Furans/chemistry , HeLa Cells , Humans , Lignans/chemistry , Models, Molecular , Stereoisomerism
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