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1986-81-8

中文名称 N-氧代烟酰胺
英文名称 Nicotinamide-N-oxide
CAS 1986-81-8
EINECS 编号 217-859-4
分子式 C6H6N2O2
MDL 编号 MFCD00006202
分子量 138.12
MOL 文件 1986-81-8.mol
更新日期 2024/10/28 17:14:48
1986-81-8 结构式 1986-81-8 结构式

基本信息

中文别名
烟酰胺氮氧化物
N-氧代烟酰胺
烟酰胺-N-氧化物
烟碱-N-氧化物
英文别名
1-OXY-NICOTINAMIDE
3-(AMINOCARBONYL)PYRIDINIUM-1-OLATE
AKOS 94294
NICOTINAMIDE 1-OXIDE
NICOTINAMIDE N-OXIDE
TIMTEC-BB SBB004187
3-Pyridinecarboxamide, 1-oxide
3-Pyridinecarboxamide,1-oxide(9CI)
1-Oxidopyridin-1-ium-3-carboxamide
Nicotinamide-N-oxide ,98%
3-Carbamoylpyridine 1-oxide
3-Pyridinecarbamide 1-oxide
所属类别
生物化工:核苷酸及其类似物

物理化学性质

熔点291-293 °C (dec.)(lit.)
沸点253.51°C (rough estimate)
密度1.3471 (rough estimate)
折射率1.5100 (estimate)
储存条件Inert atmosphere,Room Temperature
溶解度可溶于DMSO(略微加热)、甲醇(略微加热)
酸度系数(pKa)14.38±0.50(Predicted)
形态固体
颜色白色至灰白色
敏感性吸湿性
检测方法HPLC,NMR

安全数据

危险性符号(GHS)GHS hazard pictograms
GHS07
警示词警告
危险性描述H315-H319-H335
危险品标志Xi
危险类别码R36/37/38
安全说明S26-S36
WGK Germany3
海关编码29339900

应用领域

用途1
烟酰胺N-氧化物是烟酸类相关化合物,用于烟酸相关粒细胞分化的机制的研究 如人类早幼粒细胞性白血病细胞(HL-60)。烟酰胺N-氧化物减少对HL-60细胞株中c-myc的表达。

化学品安全说明书(MSDS)

N-氧代烟酰胺价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/08/19H61292烟酰胺 N-氧化物, 98%
Nicotinamide N-oxide, 98%
1986-81-825g4077元
2024/08/19H61292烟酰胺 N-氧化物, 98%
Nicotinamide N-oxide, 98%
1986-81-8100g11587元
2024/08/19N0669烟碱N-氧化物
Nicotinamide N-Oxide
1986-81-85G210元

常见问题列表

生物活性
Nicotinamide N-oxide是生物体内烟酰胺分解代谢物, 是高效选择性的CXCR2受体拮抗剂。
靶点

CXCR2

Human Endogenous Metabolite

体外研究

Nicotinamide is one of the forms of vitamin B 3 . 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. 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 (IC 50 =10 nM). Compound 2 is a selective antagonist of IL-8 binding (IC 50 =110 nM) and potent inhibitor of neutrophil chemotaxis (IC 50 =170 nM).

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