Microscopic Protonation Equilibria of Oxidized Glutathione
Author:
Affiliation:
1. Department of Pharmaceutical Chemistry, Semmelweis University, H-1092 Budapest, Högyes E. u. 9, Hungary
2. Department of Inorganic and Analytical Chemistry, Loránd Eötvös University, H-1117 Budapest, Pázmány Péter sétány 1/a, Hungary
Publisher
American Chemical Society (ACS)
Subject
Materials Chemistry,Surfaces, Coatings and Films,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp0340820
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1. Bimanes. 17. (Haloalkyl)-1,5-diazabicyclo[3.3.O]octadienediones (halo-9,10-dioxabimanes): reactivity toward the tripeptide thiol, glutathione
2. Thiolytic decomposition of the carcinogen N-methyl-N'-nitro-N-nitrosoguanidine. A change in rate-limiting step with nucleophile basicity controls alkylating activity
3. Reactions of Glutathione with Carcinogenic Esters of N-Arylhydroxamic Acids
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