Amidoximes and Oximes: Synthesis, Structure, and Their Key Role as NO Donors.
Fiche publication
Date publication
juillet 2019
Journal
Molecules (Basel, Switzerland)
Auteurs
Membres identifiés du Cancéropôle Est :
Pr SCHNEIDER Raphaël, Dr ARRAULT Axelle
Tous les auteurs :
Sahyoun T, Arrault A, Schneider R
Lien Pubmed
Résumé
Nitric oxide (NO) is naturally synthesized in the human body and presents many beneficial biological effects; in particular on the cardiovascular system. Recently; many researchers tried to develop external sources to increase the NO level in the body; for example by using amidoximes and oximes which can be oxidized in vivo and release NO. In this review; the classical methods and most recent advances for the synthesis of both amidoximes and oximes are presented first. The isomers of amidoximes and oximes and their stabilities will also be described; ()-amidoximes and ()-oximes being usually the most energetically favorable isomers. This manuscript details also the biomimetic and biological pathways involved in the oxidation of amidoximes and oximes. The key role played by cytochrome P450 or other dihydronicotinamide-adenine dinucleotide phosphate (NADPH)-dependent reductase pathways is demonstrated. Finally, amidoximes and oximes exhibit important effects on the relaxation of both aortic and tracheal rings alongside with other effects as the decrease of the arterial pressure and of the thrombi formation.
Mots clés
amidoxime, isomerism, nitric oxide, oxidation, oxime, synthesis
Référence
Molecules. 2019 Jul 5;24(13):