Journal of Asian natural products research

Synthesis and cytotoxic activities of a series of novel N-methyl-bisindolylmaleimide amide derivatives

K Wang, ZZ Liu

Index: Wang, Ke; Liu, Zhan-Zhu Journal of Asian Natural Products Research, 2014 , vol. 16, # 3 p. 296 - 303

Full Text: HTML

Citation Number: 0

Abstract

A novel series of N-methyl-bisindolylmaleimides were synthesized and evaluated for their inhibitory activities against nine tumor cell lines. Some of the compounds showed an interesting activity against the tested cell lines. The most potent compounds 5e and 5j displayed antiproliferative activity with 50% inhibitory concentration values in the μM range against some tested cell lines.

Related Articles:

Ferrocenyl Maleimides–Synthesis,(Spectro??) Electrochemistry, and Solvatochromism

[European Journal of Inorganic Chemistry, , # 7 p. 1114 - 1121]

Revised structures of N-substituted dibrominated pyrrole derivatives and their polymeric products. Termaleimide models with low optical band gaps

[Choi, Dong-Sook; Huang, Shenlin; Huang, Mingsheng; Barnard, Thomas S.; Adams, Richard D.; Seminario, Jorge M.; Tour, James M. Journal of Organic Chemistry, 1998 , vol. 63, # 8 p. 2646 - 2655]

Position-addressable nano-scaffolds. I. The preparation of N, O-, N, C-and N, N-bridged sesquinorbornadiene succinimides as compact, highly functionalized …

[Australian Journal of Chemistry, , vol. 56, # 4 p. 263 - 267]

More Articles...