Nitroso Group Transfer in S-Nitrosocysteine:  Evidence of a New Decomposition Pathway for Nitrosothiols

• Published in: Journal of organic chemistry Vol. 70; no. 16; pp. 6353 - 6361
• Main Authors: Adam, Claudia, García-Río, Luis, Leis, José Ramón, Ribeiro, Lara
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 05.08.2005
• Subjects: Chemistry; Cysteine - analogs & derivatives; Cysteine - chemistry; Exact sciences and technology; Hydrogen-Ion Concentration; Kinetics; Kinetics and mechanisms; Molecular Structure; Nitric Oxide Donors - chemistry; Organic chemistry; Protons; Reactivity and mechanisms; S-Nitrosothiols - chemistry; Sulfur - chemistry; Nitroso compound; Thionitroso compound; Aminoacid; Reaction mechanism; Decomposition; Acid catalysis; Kinetics; Reaction rate
• ISSN: 0022-3263; 1520-6904
• DOI: 10.1021/jo050811r

The rate of S-nitrosocysteine decomposition in a pH range between 0.7 < pH < 13 exhibits first- and second-order dependence on total cysteine concentration. The second-order term is only observed for pH values between 6.9 < pH < 12. Both first- and second-order terms show a complex dependence on the acidity of the medium. They increase with increasing pH, reaching a maximum value around pH = 8 and then decrease with further increase in pH. An analysis of the reaction products reveals the absence of nitrite ion and ammonia. No evidence of catalysis by copper ions is observed. These results suggest the existence of a new decomposition pathway for S-nitrosocysteine, which proceeds via an intramolecular nitroso group transfer producing a primary N-nitrosamine that decomposes rapidly to give the corresponding diazonium salt. The nitroso group transfer reaction occurs intermolecularly for the decomposition pathway exhibiting a quadratic dependence on cysteine concentration. Both nitroso group transfer pathways are subject to acid catalysis by cysteine. Kinetic results indicate that the extent of S···NO bond cleavage in the transition state is ahead of protonation of the AH···S sulfur atom. The results obtained show the existence of a new decomposition pathway for the S-nitrosocysteine where NO is not released, and hence, it has a significant biological impact due to the potential use of nitrosothiols as NO donors.