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Kinetics of Azanone (HNO) Reactions with Thiols: Effect of pH.
Smulik-Izydorczyk, Renata; Debowska, Karolina; Rostkowski, Michal; Adamus, Jan; Michalski, Radoslaw; Sikora, Adam.
Afiliação
  • Smulik-Izydorczyk R; Institute of Applied Radiation Chemistry, Lodz University of Technology, Lodz, Poland.
  • Debowska K; Institute of Applied Radiation Chemistry, Lodz University of Technology, Lodz, Poland.
  • Rostkowski M; Institute of Applied Radiation Chemistry, Lodz University of Technology, Lodz, Poland.
  • Adamus J; Institute of Applied Radiation Chemistry, Lodz University of Technology, Lodz, Poland.
  • Michalski R; Institute of Applied Radiation Chemistry, Lodz University of Technology, Lodz, Poland.
  • Sikora A; Institute of Applied Radiation Chemistry, Lodz University of Technology, Lodz, Poland. adam.sikora@p.lodz.pl.
Cell Biochem Biophys ; 79(4): 845-856, 2021 Dec.
Article em En | MEDLINE | ID: mdl-33950351
ABSTRACT
HNO (nitroxyl, IUPAC name azanone) is an electrophilic reactive nitrogen species of growing pharmacological and biological significance. Here, we present data on the pH-dependent kinetics of azanone reactions with the low molecular thiols glutathione and N-acetylcysteine, as well as with important serum proteins bovine serum albumin and human serum albumin. The competition kinetics method used is based on two parallel HNO reactions with RSH/RS- or with O2. The results provide evidence that the reaction of azanone with the anionic form of thiols (RS-) is favored over reactions with the protonated form (RSH). The data are supported with quantum mechanical calculations. A comprehensive discussion of the HNO reaction with thiolates is provided.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos de Sulfidrila Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos de Sulfidrila Idioma: En Ano de publicação: 2021 Tipo de documento: Article