Kinetic Study on the Reactivity of Azanone (HNO) toward Cyclic C-Nucleophiles

Int J Mol Sci. 2021 Nov 30;22(23):12982. doi: 10.3390/ijms222312982.

Abstract

Azanone (HNO) is an elusive electrophilic reactive nitrogen species of growing pharmacological and biological significance. Here, we present a comparative kinetic study of HNO reactivity toward selected cyclic C-nucleophiles under aqueous conditions at pH 7.4. We applied the competition kinetics method, which is based on the use of a fluorescein-derived boronate probe FlBA and two parallel HNO reactions: with the studied scavenger or with O2 (k = 1.8 × 104 M-1s-1). We determined the second-order rate constants of HNO reactions with 13 structurally diverse C-nucleophiles (k = 33-20,000 M-1s-1). The results show that the reactivity of HNO toward C-nucleophiles depends strongly on the structure of the scavenger. The data are supported with quantum mechanical calculations. A comprehensive discussion of the HNO reaction with C-nucleophiles is provided.

Keywords: Angeli’s salt; C-nucleophiles; azanone; boronate probe; peroxynitrite.

MeSH terms

  • Boronic Acids / chemistry*
  • Cyclohexanones / chemistry*
  • Hydroxamic Acids / chemistry*
  • Nitrates / chemistry
  • Nitrogen Oxides / chemistry*
  • Peroxynitrous Acid / chemistry
  • Reactive Nitrogen Species / chemistry*
  • Sulfonamides / chemistry*

Substances

  • Boronic Acids
  • Cyclohexanones
  • Hydroxamic Acids
  • Nitrates
  • Nitrogen Oxides
  • Reactive Nitrogen Species
  • Sulfonamides
  • Peroxynitrous Acid
  • Piloty's acid
  • 1,3-cyclohexanedione
  • sodium nitrate
  • nitroxyl