1. Academic Validation
  2. Design, synthesis and cytotoxic activity of novel spin-labeled rotenone derivatives

Design, synthesis and cytotoxic activity of novel spin-labeled rotenone derivatives

  • Bioorg Med Chem Lett. 2012 Jan 15;22(2):920-3. doi: 10.1016/j.bmcl.2011.12.024.
Ying-Qian Liu 1 Emika Ohkoshi Lin-Hai Li Liu Yang Kuo-Hsiung Lee
Affiliations

Affiliation

  • 1 School of Pharmacy, Lanzhou University, Lanzhou 730000, PR China; Chinese Medicine Research and Development Center, China Medical University and Hospital, Taichung, Taiwan.
Abstract

Three series of novel spin-labeled rotenone derivatives were synthesized and evaluated for cytotoxicity against four tumor cell lines, A-549, DU-145, KB and KBvin. All of the derivatives showed promising in vitro cytotoxic activity against the tumor cell lines tested, with IC(50) values ranging from 0.075 to 0.738μg/mL. Remarkably, all of the compounds were more potent than paclitaxel against KBvin in vitro, and compounds 3a and 3d displayed the highest cytotoxicity against this cell line (IC(50) 0.075 and 0.092μg/mL, respectively). Based on the observed cytotoxicity, structure-activity relationships have been described.

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