One-electron-reduction potentials of pyrimidine bases, nucleosides, and nucleotides in aqueous solution. Consequences for DNA redox chemistry

S. Steenken; J. P. Telo; H. M. Novais; L. P. Candeias

doi:10.1021/ja00038a037

One-electron-reduction potentials of pyrimidine bases, nucleosides, and nucleotides in aqueous solution. Consequences for DNA redox chemistry

Journal of the American Chemical Society ◽

10.1021/ja00038a037 ◽

1992 ◽

Vol 114 (12) ◽

pp. 4701-4709 ◽

Cited By ~ 161

Author(s):

S. Steenken ◽

J. P. Telo ◽

H. M. Novais ◽

L. P. Candeias

Keyword(s):

Aqueous Solution ◽

Redox Chemistry ◽

Reduction Potentials ◽

Pyrimidine Bases ◽

Electron Reduction

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ChemInform Abstract: One-Electron-Reduction Potentials of Pyrimidine Bases, Nucleosides, and Nucleotides in Aqueous Solution. Consequences for DNA Redox Chemistry.

ChemInform ◽

10.1002/chin.199237301 ◽

2010 ◽

Vol 23 (37) ◽

pp. no-no

Author(s):

S. STEENKEN ◽

J. P. TELO ◽

H. M. NOVAIS ◽

L. P. CANDEIAS

Keyword(s):

Aqueous Solution ◽

Redox Chemistry ◽

Reduction Potentials ◽

Pyrimidine Bases ◽

Electron Reduction

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ChemInform Abstract: Redox Chemistry of Substituted Benzenes. The One-Electron Reduction Potentials of Methoxy-Substituted Benzene Radical Cations

ChemInform ◽

10.1002/chin.199406085 ◽

2010 ◽

Vol 25 (6) ◽

pp. no-no

Author(s):

M. JONSSON ◽

J. LIND ◽

T. REITBERGER ◽

T. E. ERIKSEN ◽

G. MERENYI

Keyword(s):

Radical Cations ◽

Redox Chemistry ◽

Substituted Benzenes ◽

Reduction Potentials ◽

Electron Reduction ◽

The One

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How Easily Oxidizable Is DNA? One-Electron Reduction Potentials of Adenosine and Guanosine Radicals in Aqueous Solution

Journal of the American Chemical Society ◽

10.1021/ja962255b ◽

1997 ◽

Vol 119 (3) ◽

pp. 617-618 ◽

Cited By ~ 791

Author(s):

Steen Steenken ◽

Slobodan V. Jovanovic

Keyword(s):

Aqueous Solution ◽

Reduction Potentials ◽

Electron Reduction

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Accurate Prediction of One-Electron Reduction Potentials in Aqueous Solution by Variable-Temperature H-Atom Addition/Abstraction Methodology

The Journal of Physical Chemistry Letters ◽

10.1021/acs.jpclett.5b02452 ◽

2015 ◽

Vol 7 (1) ◽

pp. 7-13 ◽

Cited By ~ 17

Author(s):

Daniel Bím ◽

Lubomír Rulíšek ◽

Martin Srnec

Keyword(s):

Aqueous Solution ◽

Variable Temperature ◽

Accurate Prediction ◽

Reduction Potentials ◽

Electron Reduction

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Redox chemistry of substituted benzenes: the one-electron reduction potentials of methoxy-substituted benzene radical cations

The Journal of Physical Chemistry ◽

10.1021/j100145a027 ◽

1993 ◽

Vol 97 (43) ◽

pp. 11278-11282 ◽

Cited By ~ 52

Author(s):

M. Jonsson ◽

J. Lind ◽

T. Reitberger ◽

T. E. Eriksen ◽

G. Merenyi

Keyword(s):

Radical Cations ◽

Redox Chemistry ◽

Substituted Benzenes ◽

Reduction Potentials ◽

Electron Reduction ◽

The One

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Calculation of two-electron reduction potentials for some quinone derivatives in aqueous solution using Møller–Plesset perturbation theory

Journal of Molecular Structure THEOCHEM ◽

10.1016/j.theochem.2005.11.011 ◽

2006 ◽

Vol 759 (1-3) ◽

pp. 245-247 ◽

Cited By ~ 17

Author(s):

Mansoor Namazian ◽

Samira Siahrostami ◽

Mohammad R. Noorbala ◽

Michelle L. Coote

Keyword(s):

Aqueous Solution ◽

Perturbation Theory ◽

Reduction Potentials ◽

Electron Reduction ◽

Moller Plesset ◽

Plesset Perturbation Theory

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Inhibition of plant fatty acid synthesis by nitroimidazoles

Biochemical Journal ◽

10.1042/bj1980193 ◽

1981 ◽

Vol 198 (1) ◽

pp. 193-198 ◽

Cited By ~ 2

Author(s):

A V Jones ◽

J L Harwood ◽

M R Stratford ◽

P K Stumpf

Keyword(s):

Fatty Acid ◽

Fatty Acid Synthesis ◽

Soluble Fraction ◽

Acid Synthesis ◽

Long Chain Fatty Acids ◽

Reduction Potentials ◽

Marked Inhibition ◽

Mechanism Of Inhibition ◽

Pea Seeds ◽

Electron Reduction

1. The effect of the addition of a number of nitroimidazoles was tested on fatty acid synthesis by germinating pea seeds, isolated lettuce chloroplasts and a soluble fraction from pea seeds. 2. All the compounds tested had a marked inhibition on stearate desaturation by lettuce chloroplasts and on the synthesis of very-long-chain fatty acids by pea seeds. 3. In contrast, the effect of the drugs on total fatty acid synthesis from [14C]acetate in chloroplasts was related to the compound's electron reduction potentials. 4. Of the compounds used, only metronidazole had a marked inhibition on palmitate elongation in the systems tested. 5. The mechanism of inhibition of plant fatty acid synthesis by nitroimidazoles is discussed and the possible relevance of these findings to their neurotoxicity is suggested.

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