Issue 9, 2010

Synthesis, spectroscopic and DNA alkylating properties of malondialdehyde (MDA) bis-imine fluorescent adducts

Abstract

The synthesis of a series of malondialdehyde (MDA) fluorescent adducts that mimic the well-known pentamethine cyanine dyes is reported. This new subclass of bis-imino dyes shares some common spectroscopic properties with their polymethine analogues although absorbing at significantly shorter wavelengths. A small library of trimethine and pentamethine cyanine dye bis-imino analogues have been synthesised and characterised that cover a spectral range from blue to orange. Of particular interest is their capacity to act as mono- and bis-alkylating agents of nucleosides in general and of cytidine (and 2′-deoxycytidine) in particular.

Graphical abstract: Synthesis, spectroscopic and DNA alkylating properties of malondialdehyde (MDA) bis-imine fluorescent adducts

Article information

Article type
Paper
Submitted
01 Feb 2010
Accepted
31 Mar 2010
First published
14 May 2010

Mol. BioSyst., 2010,6, 1694-1699

Synthesis, spectroscopic and DNA alkylating properties of malondialdehyde (MDA) bis-imine fluorescent adducts

K. Meguellati, M. Spichty and S. Ladame, Mol. BioSyst., 2010, 6, 1694 DOI: 10.1039/C002157A

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