Thiol-dependent DNA cleavage by 3 H -1,2-benzodithiol-3-one 1,1-dioxide
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry
Reference27 articles.
1. Reaction of n-Propanethiol with 3H-1,2-Benzodithiol-3-one 1-Oxide and 5,5-Dimethyl-1,2-dithiolan-3-one 1-Oxide: Studies Related to the Reaction of Antitumor Antibiotic Leinamycin with DNA
2. 1,2-Dithiolan-3-one 1-Oxides: A Class of Thiol-Activated DNA-Cleaving Agents That Are Structurally Related to the Natural Product Leinamycin
3. Thiol-Mediated DNA Alkylation by the Novel Antitumor Antibiotic Leinamycin
4. Oxidative DNA Cleavage by the Antitumor Antibiotic Leinamycin and Simple 1,2-Dithiolan-3-one 1-Oxides: Evidence for Thiol-Dependent Conversion of Molecular Oxygen to DNA-Cleaving Oxygen Radicals Mediated by Polysulfides
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1. Synthesis and DNA Cleavage Activity of Cationic Methylene-Blue-Backboned Polymers;ACS Applied Bio Materials;2023-05-19
2. Unconventional sulfur transfer behaviour of 4-hydroxy-dithiocoumarin: an easy access to biologically potent 1,2-dithiolane scaffolds;New Journal of Chemistry;2023
3. DNA-Interactive Agents;The Organic Chemistry of Drug Design and Drug Action;2014
4. 3H-1,2-Benzodithiol-3-one 1,1-dioxide;Encyclopedia of Reagents for Organic Synthesis;2012-09-14
5. Noncovalent DNA Binding Drives DNA Alkylation by Leinamycin: Evidence That the Z,E-5-(Thiazol-4-yl)-penta-2,4-dienone Moiety of the Natural Product Serves as an Atypical DNA Intercalator;Journal of the American Chemical Society;2011-10-18
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