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