Issue 10, 2004

Synthesis of diphenylcarbazoles as cytotoxic DNA binding agents

Abstract

We report the synthesis of a series of novel diphenylcarbazoles designed to interact with DNA. The compounds bearing two or three dimethylaminoalkyloxy side chains were found to bind much more tightly to DNA, preferentially at AT-rich sites, than the corresponding hydroxy compounds. The DNA binding compounds exhibit potent cytotoxic activity toward P388 leukemia cells. The 3,6-diphenylcarbazole thus represent an interesting scaffold to develop antitumor agents interacting with nucleic acids.

Graphical abstract: Synthesis of diphenylcarbazoles as cytotoxic DNA binding agents

Article information

Article type
Paper
Submitted
30 Jan 2004
Accepted
23 Mar 2004
First published
19 Apr 2004

Org. Biomol. Chem., 2004,2, 1476-1483

Synthesis of diphenylcarbazoles as cytotoxic DNA binding agents

U. Jacquemard, S. Routier, A. Tatibouët, J. Kluza, W. Laine, C. Bal, C. Bailly and J. Mérour, Org. Biomol. Chem., 2004, 2, 1476 DOI: 10.1039/B401445F

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