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Synthesis and cytotoxicity of longistylin C derivatives.

Chinese journal of natural medicines (2015-04-25)
Yan Shan, Ting Hong, Yan-Fei Wang, Nen-Ling Zhang, Bo Yu, Yu Lu, Sheng-Xiang Qiu
RESUMEN

The present study was designed to identify potent anti-tumor compounds from a series of new longistylin C derivatives. Ten longistylin C derivatives were synthesized and their structures were confirmed by (1)H NMR, MS, and elemental analyses. Their cytotoxicity in vitro against three human cancer cell lines (A549, HepG2, and MCF-7) were evaluated by the MTT assay. Among these compounds, DT-6 and DT-9 displayed much better cytotoxicity against A549, HepG2, and MCF-7 cells, DT-1 exhibited selective cytotoxicity against HepG2, and the structure-activity relationships were investigated. In conclusion, Compounds DT-6 and DT-9 may serve as potential lead compounds for the discovery of new anti-cancer drugs.

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Sigma-Aldrich
Tetramethylsilane, ≥99.0% (GC)
Sigma-Aldrich
Tetramethylsilane, electronic grade, ≥99.99% trace metals basis