Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Nitrosyl formation, nitric oxide chemical

Despite intense study of the chemical reactivity of the inorganic NO donor SNP with a number of electrophiles and nucleophiles (in particular thiols), the mechanism of NO release from this drug also remains incompletely understood. In biological systems, both enzymatic and non-enzymatic pathways appear to be involved [28]. Nitric oxide release is thought to be preceded by a one-electron reduction step followed by release of cyanide, and an inner-sphere charge transfer reaction between the ni-trosonium ion (NO+) and the ferrous iron (Fe2+). Upon addition of SNP to tissues, formation of iron nitrosyl complexes, which are in equilibrium with S-nitrosothiols, has been observed. A membrane-bound enzyme may be involved in the generation of NO from SNP in vascular tissue [35], but the exact nature of this reducing activity is unknown. [Pg.293]


See other pages where Nitrosyl formation, nitric oxide chemical is mentioned: [Pg.51]    [Pg.204]    [Pg.329]    [Pg.146]    [Pg.613]    [Pg.614]    [Pg.72]    [Pg.202]    [Pg.217]    [Pg.168]    [Pg.83]    [Pg.117]    [Pg.16]    [Pg.390]    [Pg.391]    [Pg.595]    [Pg.715]    [Pg.932]    [Pg.110]    [Pg.421]    [Pg.3875]   


SEARCH



Chemical oxidants

Chemical oxidation

Chemical oxidizers

Chemicals oxidizing

Nitric formation

Nitrosyl formate

© 2024 chempedia.info