New Method of Synthesis and Biological Evaluation of Some Combretastatin A-4 Analogues
摘要:
A series of novel combretastatin A-4 analogues was synthesized in 36-64% yields by Negishi cross-coupling reaction under mild conditions. The prepared compounds exhibit good cytotoxicity against HBL100 epithelial cell lines (IC50 = 0.022-10.31 mu M).
Tubulin Binding Anti Cancer Agents And Prodrugs Thereof
申请人:Matteucci Mark
公开号:US20090042820A1
公开(公告)日:2009-02-12
Novel tubulin binding compounds and hypoxia activated prodrugs of novel and known tubulin binding compounds useful for treating cancer and other hyperproliferative diseases are disclosed.