Nicotinamide N-oxide

(Synonyms: 烟酰胺-N-氧化物)
目录号: PC63064 纯度: 10mM*1mLinDMSO
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。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。
CAS No. :1986-81-8
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中文名称
Nicotinamide N-oxide
中文别名
N-氧代烟酰胺;烟酰胺-N-氧化物;烟碱-N-氧化物;烟碱 N-氧化物;Nicotinamide N-Oxide 烟碱 N-氧化物;N-氧代烟酰胺,Nicotinamide-N-oxide;烟酰胺 N-氧化物;烟酰胺氮氧化物;N-氧化烟酰胺;尼克酰胺N氧化物;烟酰胺-N-氧化物 N-氧代烟酰胺;烟碱-N-氧化物,98%
英文名称
Nicotinamide N-oxide
英文别名
Nicotinamide-N-oxide;1-Oxynicotinamide;Nicotinamide N-Oxide;1-oxidopyridin-1-ium-3-carboxamide;1-Oxy-nicotinamide;3-(AMINOCARBONYL)PYRIDINIUM-1-OLATE;3-carbamoylpyridine 1-oxide;3-Pyridincarboxamid-1-oxid;3-Pyridinecarboxamide,1-oxide;3-Pyridinecarboxamide,Oxynicotinamide;nicotinamide N1-oxide;Nicotinamide,1-oxide;Nicotinic acid amide N-oxide;AKOS 94294;Oxynicotinamide;TIMTEC-BB SBB004187;3-Pyridinecarbamide 1-oxide;NICOTINAMIDE 1-OXIDE;Nicotinamide-N-oxide ,98%;3-Pyridinecarboxamide, 1-oxide;niacinamide-n-oxide;Nicotinamide, 1-oxide;3-carbamoylpyridin-1-ium-1-olate;1-oxide-nicotinamide;6UY6QXJ2DP;1-oxide-(8CI)-nicotinamide;1-oxide-
Cas No.
1986-81-8
分子式
C6H6N2O2
分子量
138.12
包装储存
Powder; -20°C; 3 years; 4°C; 2 years;
详情描述
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。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。
生物活性
Nicotinamide N-oxide, an in vivo nicotinamide metabolite, is a potent, and selective antagonist of the CXCR2 receptor.
性状
Solid
IC50 & Target[1][2]
Human Endogenous Metabolite
 CXCR2
 
体外研究(In Vitro)
Nicotinamide 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. 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).
运输条件
Room temperature or refrigerated transport.
储存方式
Powder; -20°C; 3 years; 4°C; 2 years;
结构分类
Alkaloids
Pyridin
溶解度数据
体外研究:
H2O : 20 mg/mL(144.80 mM;Need ultrasonic)
DMSO : 10 mg/mL(72.40 mM;Need ultrasonic)
配制储存液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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