Synthesis and cytotoxicity of novel 20-O-linked homocamptothecin ester derivatives as potent topoisomerase I inhibitors

DZ Li, CY Wang, RH Liu, YM Wang, TF Ji…

Index: Li, Di-Zao; Wang, Cun-Ying; Liu, Rui-Hua; Wang, Yan-Ming; Ji, Teng-Fei; Li, Yu-Rong; Pan, Xian-Dao Journal of Asian Natural Products Research, 2013 , vol. 15, # 11 p. 1179 - 1188

Full Text: HTML

Citation Number: 0

Abstract

In an attempt to improve the antitumor activity of homocamptothecins (hCPTs), a series of novel 20-O-linked hCPT ester derivatives were first designed and synthesized based on a synthetic route, by which hCPTs are acylated with different substituted phenoxyacetic acid ester derivatives. Most of the derivatives were assayed for in vitro cytotoxicity against six human cancer cell lines KB, KB/VCR, A549, HCT-8, Bel7402, and A2780, and most of the ...

Related Articles:

BN 80245: an E-ring modified camptothecin with potent antiproliferative and topoisomerase I inhibitory activities

[Lavergne, Olivier; Lesueur-Ginot, Laurence; Rodas, Francesc Pla; Bigg, Dennis C. H. Bioorganic and Medicinal Chemistry Letters, 1997 , vol. 7, # 17 p. 2235 - 2238]

More Articles...