Petzold, Holm and Sadler, P. J.. (2008) Oxidation induced by the antioxidant glutathione (GSH). Chemical Communications (No.37). pp. 4413-4415. ISSN 1359-7345

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Abstract

Remarkably efficient oxygen atom transfer from an intermediate of glutathione (GSH) autoxidation to an organometallic ruthenium arene thiolato complex is observed under physiologically-relevant conditions.

Item Type:	Journal Article
Subjects:	Q Science > QD Chemistry
Divisions:	Faculty of Science > Chemistry
Library of Congress Subject Headings (LCSH):	Glutathione, Oxidation, Organometallic compounds, Ruthenium compunds
Journal or Publication Title:	Chemical Communications
Publisher:	Royal Society of Chemistry
ISSN:	1359-7345
Date:	7 October 2008
Number:	No.37
Number of Pages:	3
Page Range:	pp. 4413-4415
Identification Number:	10.1039/b805358h
Status:	Peer Reviewed
Publication Status:	Published
Access rights to Published version:	Restricted or Subscription Access
Funder:	Deutscher Akademischer Austauschdienst (DAAD), Research Councils UK (RCUK)
Grant number:	D/06/45748 (DAAD)
References:	1 A. Corazza, I.Harvey and P. J. Sadler, Eur. J. Biochem., 1996, 236, 697. 2 A. Meister, J. Biol. Chem., 1988, 263, 17205. 3 A. Meister and M. E. Anderson, Annu. Rev. Biochem., 1983, 52, 711. 4 B. Halliwell and J. M. C. Gutteridge, Free radicals in biology and medicine. Oxford University Press, Oxford, 1999. 5 A. Meister, A brief history of glutathione and a survey of its metabolism and functions, , in Coenzymes and Cofactors, ed. D. Dolphin, R. Poulson and O. Avramovic, Wiley, New York, 1988, pp. 1–48. 6 A. Krezel, W. Szczepanik, M. Soko"owska, M. Jezowska-Bojczuk and W. Bal, Chem. Res. Toxicol., 2003, 16, 855. 7 J. Reedijk, Proc. Natl. Acad. Sci. U. S. A., 2003, 100, 3611. 8 Y.-K. Yan, M. Melchart, A. Habtemariam and P. J. Sadler, Chem. Commun., 2005, 4764. 9 F. Wang, A. Habtemariam, E. P. L. van der Geer, R. Ferna´ ndez, M. Melchart, R. J. Deeth, R. Aird, S. Guichard, F. P. A. Fabbiani, P. Lozano-Casal, I. D. H. Oswald, D. I. Jodrell, S. Parsons and P. J. Sadler, Proc. Natl. Acad. Sci. U. S. A., 2005, 102, 18269. 10 H. Petzold, J. Xu and P. J. Sadler, Angew. Chem., Int. Ed., 2008, 47, 3008. 11 F. Wang, J. Xu, A. Habtemariam, J. Bella and P. J. Sadler, J. Am. Chem. Soc., 2005, 127, 17734. 12 F. Wang, H. Chen, J. A. Parkinson, P. d. S. Murdoch and P. J. Sadler, Inorg. Chem., 2002, 41, 4509. 13 P. A. Vesilind, Introduction to environmental engineering, PWS Publishing Company, Boston, 1996. 14 Other possible reaction pathways could involve formation of superoxide radicals (O2 ) via thiyl radicals (RS); for a general review see ref. 22 and literature cited therein. 15 T. V. Votyakovaa and I. J. Reynolds, Arch. Biochem. Biophys., 2004, 431, 138. 16 C. Galvez, D. G. Ho, A. Azod and M. Selke, J. Am. Chem. Soc., 2001, 123, 3381. 17 C. A. Grappenhaus and M. Y. Darensbourg, Acc. Chem. Res., 1998, 31, 451. 18 W. Weigand, G. Bosl, B. von Dielingen and K. Gollnick, Z. Naturforsch., B: Chem. Sci., 1994, 49, 513. 19 S. M. Bonesi, M. Fagnoni, S. Monti and A. Albini, Tetrahedron, 2006, 62, 10716. 20 E. L. Clennan and C. Liao, Tetrahedron, 2006, 62, 10724. 21 F. Jensen, A. Greer and E. L. Clennan, J. Am. Chem. Soc., 1998, 120, 4439. 22 U. Muenchberg, A. Anwar, S. Mecklenburg and C. Jacob, Org. Biomol. Chem., 2007, 5, 1505. 23 C. Jacob, Nat. Prod. Rep., 2006, 23, 851.
URI:	http://wrap.warwick.ac.uk/id/eprint/29338

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