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Metalloporphyrins as versatile catalysts for oxidation reactions and oxidative DNA cleavage

Bernard Meunier
- 01 Sep 1992 - 
- Vol. 92, Iss: 6, pp 1411-1456
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This article is published in Chemical Reviews.The article was published on 1992-09-01. It has received 1930 citations till now.

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A simple copper(II)-L-histidine system for efficient hydrolytic cleavage of DNA.

TL;DR: Study of the mechanism of plasmid DNA cleavage by added radical scavengers, using rigorously anaerobic experiments, analyses for malondialdehyde-like products, religation assays, and HPLC analyses, indicate thatDNA cleavage mediated by Cu(L-His) occurs via a hydrolytic path.
Journal ArticleDOI

Biomimetic modeling of oxidative drug metabolism : Strategies, advantages and limitations.

TL;DR: This review summarizes three different nonenzymatic strategies, including metalloporphyrins as surrogates of the active centre of cytochrome P450, Fenton’s reagent, and the electrochemical oxidation of drug compounds.
Journal ArticleDOI

Multiple Active Oxidants in Cytochrome P-450 Model Oxidations

TL;DR: Evidence for the existence of distinct active oxidizing species in a cytochrome P-450 model system is reported and it is proposed that the active oxidant is a complex between the catalyst and the terminal oxidant.
Journal ArticleDOI

Synthesis, crystal structure, DNA binding and photo-induced DNA cleavage activity of (S-methyl-l-cysteine)copper(II) complexes of heterocyclic bases

TL;DR: Control DNA cleavage experiments suggest major groove binding propensity for the dppz complex, while the phen and dpq complexes bind at the minor groove of DNA, and chemically significant non-covalent interactions like hydrogen bonding involving the axial aqua ligand and pi-pi interactions between dppZ ligands.
Journal ArticleDOI

Metal-catalyzed asymmetric sulfoxidation, epoxidation and hydroxylation by hydrogen peroxide

TL;DR: In this paper, the use of non-heme systems for asymmetric sulfoxidation, epoxidation and dihydroxylation of alkenes has been discussed and the possibility of asymmetric oxidation catalyzed by metalloporphyrins has also been discussed.
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