Electrochemical Properties of Substituted 2‐Methyl‐1,4‐Naphthoquinones: Redox Behavior Predictions-Reference-Cited by-同舟云学术

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Electrochemical Properties of Substituted 2‐Methyl‐1,4‐Naphthoquinones: Redox Behavior Predictions

Published:2014-12-30 Issue:8 Volume:21 Page:3415-3424
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Elhabiri Mourad¹,Sidorov Pavel²³,Cesar‐Rodo Elena¹,Marcou Gilles²,Lanfranchi Don Antoine¹,Davioud‐Charvet Elisabeth¹,Horvath Dragos²,Varnek Alexandre²³

Affiliation:

1. Laboratoire de Chimie Bioorganique et Medicinale, UMR7509 CNRS‐Université de Strasbourg, European School of Chemistry, Polymers and Materials (ECPM), 25 Rue Becquerel, F‐67087 Strasbourg (France), Fax: (+33) 3‐68‐85‐27‐42

2. Laboratoire de Chemoinformatique, UMR 7140 CNRS‐Université de Strasbourg, 1 rue Blaise Pascal, Strasbourg 67000 (France)

3. Butlerov Institute of Chemistry, Kazan Federal University, Kazan (Russia)

Funder

International Center for Frontier Research in Chemistry (ic-FRC) in Strasbourg

Centre National de la Recherche Scientifique

CNRS

the University of Strasbourg

ANRémergence program

Laboratoire d′Excellence (LabEx) ParaFrap

Program of Competitive Growth of Kazan Federal University

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201403703

Reference90 articles.

1. Electrochemical parameters and techniques in drug development, with an emphasis on quinones and related compounds

2. Mechanism of teratogenesis: Electron transfer, reactive oxygen species, and antioxidants

3. Role of Quinones in Toxicology

4. The Metabolism and Toxicity of Quinones, Quinonimines, Quinone Methides, and Quinone-Thioethers

5. The aza-analogues of 1,4-naphthoquinones are potent substrates and inhibitors of plasmodial thioredoxin and glutathione reductases and of human erythrocyte glutathione reductase

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