Istituto Pasteur - Fondazione Cenci Bolognetti, Dipartimento di Chimica e Tecnologie del Farmaco, Sapienza Università di Roma, Piazzale Aldo Moro 5, I-00185 Roma, Italy.
Eur J Med Chem. 2011 Aug;46(8):3519-25. doi: 10.1016/j.ejmech.2011.05.020. Epub 2011 May 13.
The crucial role played by microtubules in the life of eukaryotic cell makes tubulin an important route for the anticancer therapy. The Arylthioindoles (ATIs) along with the corresponding ketone and methylene compounds are potent tubulin assembly inhibitors. We are here reporting the result of a series of docking and molecular dynamics experiments on this series of compounds. The results obtained from our in silico studies not only provided us with an insight on the nature of the binding of the ATIs to tubulin, but were also at the core of the design of a new series of potent inhibitors of tubulin polymerization.
微管在真核细胞生命中的关键作用使得微管蛋白成为抗癌治疗的重要途径。芳基硫代吲哚(ATIs)及其相应的酮和亚甲基化合物是有效的微管组装抑制剂。我们在此报告了对该系列化合物进行一系列对接和分子动力学实验的结果。我们的计算机研究结果不仅使我们深入了解了 ATIs 与微管蛋白结合的性质,而且还为设计一系列新的强效微管蛋白聚合抑制剂提供了核心。