Thiyl radicals react with nitric oxide to form S-nitrosothiols with rate constants near the diffusion-controlled limit.

[1]  W. Koppenol,et al.  The glutathione thiyl radical does not react with nitrogen monoxide. , 2007, Biochemical and biophysical research communications.

[2]  E. Madej,et al.  The oxidizing power of the glutathione thiyl radical as measured by its electrode potential at physiological pH. , 2007, Archives of biochemistry and biophysics.

[3]  I. Fridovich,et al.  Kinetic properties of Cu,Zn-superoxide dismutase as a function of metal content--order restored. , 2006, Free radical biology & medicine.

[4]  E. Madej,et al.  Pulse radiolysis and cyclic voltammetry studies of redox properties of phenothiazine radicals , 2006 .

[5]  J. R. Lancaster Nitroxidative, nitrosative, and nitrative stress: kinetic predictions of reactive nitrogen species chemistry under biological conditions. , 2006, Chemical research in toxicology.

[6]  P. Wardman,et al.  Properties of the radical intermediate obtained on oxidation of 2',7'-dichlorodihydrofluorescein, a probe for oxidative stress. , 2006, Free radical biology & medicine.

[7]  N. Hogg,et al.  S‐Nitrosation of Cysteine Thiols as a Redox Signal , 2006 .

[8]  R. Radi,et al.  Corrigendum to “Tyrosine nitration by superoxide and nitric oxide fluxes in biological systems: Modeling the impact of superoxide dismutase and nitric oxide diffusion” [Free Radic. Biol. Med. 39:728–741; 2005] , 2006 .

[9]  R. Radi,et al.  Tyrosine nitration by superoxide and nitric oxide fluxes in biological systems: modeling the impact of superoxide dismutase and nitric oxide diffusion. , 2005, Free radical biology & medicine.

[10]  S. Miersch,et al.  Protein S-nitrosation: biochemistry and characterization of protein thiol-NO interactions as cellular signals. , 2005, Clinical biochemistry.

[11]  W. Koppenol,et al.  Kinetics properties of Cu,Zn-superoxide dismutase as a function of metal content. , 2005, Archives of biochemistry and biophysics.

[12]  S. Herold,et al.  Mechanistic studies of S-nitrosothiol formation by NO*/O2 and by NO*/methemoglobin. , 2005, Archives of biochemistry and biophysics.

[13]  N. Hogg,et al.  S-Nitrosothiols: cellular formation and transport. , 2005, Free radical biology & medicine.

[14]  S. Goldstein,et al.  Chemistry of peroxynitrites as compared to peroxynitrates. , 2005, Chemical reviews.

[15]  J. Pelling,et al.  Thiyl radical reaction with amino acid side chains: rate constants for hydrogen transfer and relevance for posttranslational protein modification. , 2004, Chemical research in toxicology.

[16]  L. Folkes,et al.  Kinetics of the reaction between nitric oxide and glutathione: implications for thiol depletion in cells. , 2004, Free radical biology & medicine.

[17]  S. Goldstein,et al.  Reaction of Organic Peroxyl Radicals with •NO2 and •NO in Aqueous Solution: Intermediacy of Organic Peroxynitrate and Peroxynitrite Species , 2004 .

[18]  S. Lymar,et al.  Rate of ON-OO - Bond Homolysis and the Gibbs Energy of Formation of Peroxynitrite , 2003 .

[19]  B. Mayer,et al.  S-nitrosation of glutathione by nitric oxide, peroxynitrite, and (*)NO/O(2)(*-). , 2003, Free radical biology & medicine.

[20]  E. Ford,et al.  Kinetics of the reactions of nitrogen dioxide with glutathione, cysteine, and uric acid at physiological pH. , 2002, Free radical biology & medicine.

[21]  R. Eisenthal,et al.  Reduction of Nitrite to Nitric Oxide Catalyzed by Xanthine Oxidoreductase* , 2000, The Journal of Biological Chemistry.

[22]  N. Hogg The kinetics of S-transnitrosation--a reversible second-order reaction. , 1999, Analytical biochemistry.

[23]  Barry Halliwell,et al.  Formation of nitric oxide-derived inflammatory oxidants by myeloperoxidase in neutrophils , 1998, Nature.

[24]  R. Redmond,et al.  The Mechanism of Photochemical Release of Nitric Oxide from S‐Nitrosoglutathione , 1996 .

[25]  G. Czapski,et al.  Mechanism of the Nitrosation of Thiols and Amines by Oxygenated •NO Solutions: The Nature of the Nitrosating Intermediates J. Am. Chem. Soc. 1996, 118, 3419−3425 , 1996 .

[26]  S. Mezyk Rate Constant Determination for the Reaction of Hydroxyl and Glutathione Thiyl Radicals with Glutathione in Aqueous Solution , 1996 .

[27]  S. Goldstein,et al.  MECHANISM OF THE NITROSATION OF THIOLS AND AMINES BY OXYGENATED NO SOLUTIONS : THE NATURE OF THE NITROSATING INTERMEDIATES , 1996 .

[28]  S. Goldstein,et al.  Kinetics of Nitric Oxide Autoxidation in Aqueous Solution in the Absence and Presence of Various Reductants. The Nature of the Oxidizing Intermediates , 1995 .

[29]  L. Packer,et al.  Biothiols in Health and Disease , 1995 .

[30]  J. Holcman,et al.  Reactivity of nitric oxide with simple short-lived radicals in aqueous solutions , 1994 .

[31]  G. Merényi,et al.  Kinetics of One-Electron Oxidation of Thiols and Hydrogen Abstraction by Thiyl Radicals from .alpha.-Amino C-H Bonds , 1994 .

[32]  E. Land,et al.  The glutathione free radical equilibrium, GS. + GS−⇌ GSS.−G, mediating electron transfer to FE(III) -cytochrome c , 1994 .

[33]  E. Bothe,et al.  Intramolecular transformation reaction of the glutathione thiyl radical into a non-sulphur-centred radical: a pulse-radiolysis and EPR study. , 1992, International journal of radiation biology.

[34]  T. Malinski,et al.  Nitric oxide release from a single cell measured in situ by a porphyrinic-based microsensor , 1992, Nature.

[35]  T. Eriksen,et al.  Formation of reducing radicals on radiolysis of glutathione and some related compounds in aqueous solution , 1988 .

[36]  R. Willson,et al.  Free radical induced one-electron oxidation of the phenothiazines chlorpromazine and promethazine , 1984 .

[37]  M. Hoffman,et al.  Rate constants for the reaction of the carbonate radical with compounds of biochemical interest in neutral aqueous solution. , 1973, Radiation research.

[38]  P. Wardman,et al.  The roles of thiol-derived radicals in the use of 2',7'-dichlorodihydrofluorescein as a probe for oxidative stress. , 2008, Free radical biology & medicine.

[39]  D. L. Williams,et al.  Nitrosation reactions and the chemistry of nitric oxide , 2004 .

[40]  S. Mezyk,et al.  Disulfide anion radical equilibria: effects of -NH3+, -CO2–, -NHC(O)- and -CH3 groups , 1999 .

[41]  T. Eriksen,et al.  Significance of the intramolecular transformation of glutathione thiyl radicals to α-aminoalkyl radicals. Thermochemical and biological implications , 1997 .

[42]  G. Buxton,et al.  Re-evaluation of the thiocyanate dosimeter for pulse radiolysis , 1995 .

[43]  B. Ketterer,et al.  Glutathione Conjugation: Mechanisms and Biological Significance , 1989 .

[44]  W. Pryor,et al.  Oxidation of thiols by nitric oxide and nitrogen dioxide: synthetic utility and toxicological implications , 1982 .

[45]  R. Willson,et al.  Radical-cations as reference chromogens in kinetic studies of ono-electron transfer reactions: pulse radiolysis studies of 2,2′-azinobis-(3-ethylbenzthiazoline-6-sulphonate) , 1982 .

[46]  John Aurie Dean,et al.  Lange's Handbook of Chemistry , 1978 .

[47]  A. Esfandi,et al.  Radiolysis of glutathione in oxygen-containing solutions of pH7. , 1977, International journal of radiation biology and related studies in physics, chemistry, and medicine.

[48]  E. Hayon,et al.  Pulse radiolysis study of sulfhydryl compounds in aqueous solution. , 1973 .

[49]  E. Hayon,et al.  One-electron reduction of the disulfide linkage in aqueous solution. Formation, protonation, and decay kinetics of the RSSR- radical , 1972 .

[50]  N. Klassen,et al.  PULSE RADIOLYSIS OF PENICILLAMINE IN AQUEOUS SOLUTION: THE THIYL RADICAL AND THE DISULPHIDE RADICAL ANION. , 1971 .