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Merck
  • Antitumor agents. Part 3: synthesis and cytotoxicity of new trans-stilbene benzenesulfonamide derivatives.

Antitumor agents. Part 3: synthesis and cytotoxicity of new trans-stilbene benzenesulfonamide derivatives.

Bioorganic & medicinal chemistry letters (2002-03-23)
Li-Ming Yang, Shwu-Jiuan Lin, Fen-Lin Hsu, Tsang-Hsiung Yang
摘要

A new series of trans-stilbene benzenesulfonamide derivatives were designed and synthesized as potential antitumor agents. These new compounds were evaluated in the National Cancer Institute's 60 human tumor cell line in vitro screen. Compounds 9-13 were cytotoxic against several cell lines. Notably, two compounds, 9 and 12, demonstrated selective cytotoxic activity against BT-549 breast cancer (GI(50)=0.205 microM) and HT-29 colon cancer (GI(50)=0.554 microM), respectively.

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Sigma-Aldrich
反式-1,2-二苯乙烯氧化物, 98%
Sigma-Aldrich
顺均二苯代乙烯氧化物, 97%