CAS 1986-81-8|Nicotinamide N-oxide

Introduction:Basic information about CAS 1986-81-8|Nicotinamide N-oxide, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameNicotinamide N-oxide
CAS Number1986-81-8Molecular Weight138.12400
Density1.34 g/cm3Boiling Point514.7ºC at 760 mmHg
Molecular FormulaC6H6N2O2Melting Point291-293 °C (dec.)(lit.)
MSDSChineseUSAFlash Point265.1ºC
Symbol
GHS07
Signal WordWarning

Names

Name1-oxidopyridin-1-ium-3-carboxamide
SynonymMore Synonyms

Nicotinamide N-oxide BiologicalActivity

DescriptionNicotinamide N-oxide, an in vivo nicotinamide metabolite, is a potent, and selective antagonist of the CXCR2 receptor.
Related CatalogResearch Areas >>Inflammation/ImmunologyNatural Products >>Others
Target

Human Endogenous Metabolite

In VitroNicotinamide is one of the forms of vitamin B3. It is a precursor for nicotinamide adenine dinucleotide, which is best known as an electron carrier in oxidative phosphorylation and as a cofactor for many dehydrogenases. It is metabolized through two enzymatic systems. The first system starts with the methylation of nicotinamide by nicotinamide N-methyltransferase, which can subsequently be oxidized by aldehyde oxidase. The second enzymatic system oxidizes nicotinamide to nicotinamide N-oxide[1]. A series of nicotinamide N-oxides is synthesized and shown to be novel, potent, and selective antagonists of the CXCR2 receptor. Compound 1 has demonstrated potent inhibition of neutrophil chemotaxis (IC50=10 nM). Compound 2 is a selective antagonist of IL-8 binding (IC50=110 nM) and potent inhibitor of neutrophil chemotaxis (IC50=170 nM)[2].
References

[1]. Real AM, et al. Nicotinamide N-oxidation by CYP2E1 in human liver microsomes. Drug Metab Dispos. 2013 Mar;41(3):550-3.

[2]. Cutshall NS, et al. Nicotinamide N-oxides as CXCR2 antagonists. Bioorg Med Chem Lett. 2001 Jul 23;11(14):1951-4.

Chemical & Physical Properties

Density1.34 g/cm3
Boiling Point514.7ºC at 760 mmHg
Melting Point291-293 °C (dec.)(lit.)
Molecular FormulaC6H6N2O2
Molecular Weight138.12400
Flash Point265.1ºC
Exact Mass138.04300
PSA68.55000
LogP0.91430
Vapour Pressure1.05E-10mmHg at 25°C
Index of Refraction1.602
InChIKeyUSSFUVKEHXDAPM-UHFFFAOYSA-N
SMILESNC(=O)c1ccc[n+]([O-])c1
Storage conditionRefrigerator

Safety Information

Symbol
GHS07
Signal WordWarning
Hazard StatementsH315-H319-H335
Precautionary StatementsP261-P305 + P351 + P338
Personal Protective Equipmentdust mask type N95 (US);Eyeshields;Gloves
Hazard CodesXi:Irritant;
Risk PhrasesR36/37/38
Safety PhrasesS26-S36
RIDADRNONH for all modes of transport
WGK Germany3

Articles21

More Articles
Effects of excess nicotinamide administration on the urinary excretion of nicotinamide N-oxide and nicotinuric acid by rats.

Biosci. Biotechnol. Biochem. 68(1) , 44-50, (2004)

We investigated a useful chemical index for an excessive nicotinamide intake and how this excessive nicotinamide intake affects the tryptophan-nicotinamide metabolism in rats. Weaning rats were fed on...

Pharmacokinetics and biochemistry studies on nicotinamide in the mouse.

Cancer Chemother. Pharmacol. 34(5) , 399-404, (1994)

Nicotinamide sensitizes murine tumours to the effect of radiation, but the pharmacokinetics are not well characterized at doses that are achievable in humans. In the mouse, nicotinamide given i.p. at ...

Plasma and urine pharmacokinetics of niacin and its metabolites from an extended-release niacin formulation.

Int. J. Clin. Pharmacol. Ther. 45(8) , 448-54, (2007)

To characterize plasma and urine pharmacokinetics of niacin and its metabolites after oral administration of 2,000 mg of extended-release (ER) niacin in healthy male volunteers.Niacin ER was administe...

Synonyms

3-carbamoylpyridine 1-oxide
Nicotinamide,1-oxide
nicotinamide N1-oxide
EINECS 217-859-4
3-Pyridinecarboxamide,1-oxide
1-Oxy-nicotinamide
Nicotinic acid amide N-oxide
3-Pyridincarboxamid-1-oxid
Nicotinamide N-oxide
3-Pyridinecarboxamide,Oxynicotinamide
MFCD00006202
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