Nicoxamat

General

Type : Hydroxamate

Chemical_Nomenclature : N-hydroxypyridine-3-carboxamide

Canonical SMILES : C1=CC(=CN=C1)C(=O)NO

InChI : InChI=1S\/C6H6N2O2\/c9-6(8-10)5-2-1-3-7-4-5\/h1-4,10H,(H,8,9)

InChIKey : IYCHDNQCHLMLJZ-UHFFFAOYSA-N

Other name(s) : N-Hydroxynicotinamide  ||  Nicotinohydroxamic acid  ||  N-hydroxypyridine-3-carboxamide  ||  SCHEMBL93839  ||  CHEMBL504369  ||  CHEBI:173404


MW : 138.12

Formula : C6H6N2O2

CAS_number : 5657-61-4

PubChem : 71211

UniChem : IYCHDNQCHLMLJZ-UHFFFAOYSA-N

Target

Structure : No structure

Families : No family

References (2)

Title : [On the plurifactorial determinism of the organophosphorous-induced teratogenesis on bird embryos\; trials of protection by various compounds: oximes, hydroxamic acids and nicotinamide analogs (author's transl)] - Meiniel_1979_Arch.Anat.Histol.Embryol_62_29
Author(s) : Meiniel R , Quan DQ , Autissier-Navarro C , Caujolle R , Bernadou J
Ref : Arch Anatomia Histologia Embryologia , 62 :29 , 1979
Abstract :
PubMedSearch : Meiniel_1979_Arch.Anat.Histol.Embryol_62_29
PubMedID: 161493

Title : Effect of nicotinhydroxamic acid methiodide on human plasma cholinesterase inhibited by organophosphates containing a dialkylphosphato group -
Author(s) : Hobbiger F
Ref : British Journal of Pharmacology Chemother , 10 :356 , 1955
PubMedID: 13269715