Kinetic characteristics of the reaction of natural thiols with peroxyl radicals and hydrogen peroxide
- 作者: Zinatullina K.M.1,2,3, Khrameeva N.P.2, Kasaikina O.T.1,3,4, Shapiro B.I.2, Kuzmin V.A.2,4
- 
							隶属关系: 
							- N. N. Semenov Institute of Chemical Physics, Russian Academy of Sciences
- N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
- P. G. Demidov Yaroslavl State University
- Department of Chemistry, M. V. Lomonosov Moscow State University
 
- 期: 卷 66, 编号 7 (2017)
- 页面: 1300-1303
- 栏目: Full Articles
- URL: https://journal-vniispk.ru/1066-5285/article/view/241005
- DOI: https://doi.org/10.1007/s11172-017-1888-3
- ID: 241005
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详细
Kinetic characteristics of the reaction between natural thiols, viz., glutathione, cysteine, and homocysteine, and peroxyl radicals formed upon decomposition of the azo initiator AAPH (2,2´-azobis(2-methylpropionamidine) dihydrochloride) in aqueous solutions at 37 °С were determined by the competing reaction method. The kinetics of radicals formation in the reaction between natural thiols and H2O2 was studied by the inhibitor method. The polymethine dye, pyridinium 3,3´-di-γ-sulfopropyl-9-methylthiacarbocyanine, was used as the radical scavenger. Cysteine was found to exhibit the highest activity in the reactions with peroxyl radicals and in the free radical generation upon the reaction with H2O2. The data obtained can be useful for understanding the physiological role of thiols in oxidative processes.
作者简介
K. Zinatullina
N. N. Semenov Institute of Chemical Physics, Russian Academy of Sciences; N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences; P. G. Demidov Yaroslavl State University
							编辑信件的主要联系方式.
							Email: karinazinat11@gmail.com
				                					                																			                												                	俄罗斯联邦, 							4 ul. Kosygina, Moscow, 119991; 4 ul. Kosygina, Moscow, 119991; 14 ul. Sovetskaya, Yaroslavl, 150003						
N. Khrameeva
N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
														Email: karinazinat11@gmail.com
				                					                																			                												                	俄罗斯联邦, 							4 ul. Kosygina, Moscow, 119991						
O. Kasaikina
N. N. Semenov Institute of Chemical Physics, Russian Academy of Sciences; P. G. Demidov Yaroslavl State University; Department of Chemistry, M. V. Lomonosov Moscow State University
														Email: karinazinat11@gmail.com
				                					                																			                												                	俄罗斯联邦, 							4 ul. Kosygina, Moscow, 119991; 14 ul. Sovetskaya, Yaroslavl, 150003; Build. 3, 1 Leninskie Gory, Moscow, 119992						
B. Shapiro
N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
														Email: karinazinat11@gmail.com
				                					                																			                												                	俄罗斯联邦, 							4 ul. Kosygina, Moscow, 119991						
V. Kuzmin
N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences; Department of Chemistry, M. V. Lomonosov Moscow State University
														Email: karinazinat11@gmail.com
				                					                																			                												                	俄罗斯联邦, 							4 ul. Kosygina, Moscow, 119991; Build. 3, 1 Leninskie Gory, Moscow, 119992						
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