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1986-81-8

中文名稱 N-氧代煙酰胺
英文名稱 Nicotinamide-N-oxide
CAS 1986-81-8
EINECS 編號 217-859-4
分子式 C6H6N2O2
MDL 編號 MFCD00006202
分子量 138.12
MOL 文件 1986-81-8.mol
更新日期 2025/01/06 11:09:32
1986-81-8 結(jié)構(gòu)式 1986-81-8 結(jié)構(gòu)式

基本信息

中文別名
煙酰胺氮氧化物
N-氧代煙酰胺
煙酰胺-N-氧化物
煙堿-N-氧化物
英文別名
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
所屬類別
生物化工:核苷酸及其類似物

物理化學(xué)性質(zhì)

熔點(diǎn)291-293 °C (dec.)(lit.)
沸點(diǎn)253.51°C (rough estimate)
密度1.3471 (rough estimate)
折射率1.5100 (estimate)
儲存條件Inert atmosphere,Room Temperature
溶解度可溶于DMSO(略微加熱)、甲醇(略微加熱)
酸度系數(shù)(pKa)14.38±0.50(Predicted)
形態(tài)固體
顏色白色至灰白色
敏感性吸濕性
檢測方法HPLC,NMR
CAS 數(shù)據(jù)庫1986-81-8(CAS DataBase Reference)

安全數(shù)據(jù)

危險性符號(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險性描述H315-H319-H335
危險品標(biāo)志Xi
危險類別碼R36/37/38
安全說明S26-S36
WGK Germany3
海關(guān)編碼29339900

應(yīng)用領(lǐng)域

用途1
煙酰胺N-氧化物是煙酸類相關(guān)化合物,用于煙酸相關(guān)粒細(xì)胞分化的機(jī)制的研究 如人類早幼粒細(xì)胞性白血病細(xì)胞(HL-60)。煙酰胺N-氧化物減少對HL-60細(xì)胞株中c-myc的表達(dá)。

上下游產(chǎn)品信息

化學(xué)品安全說明書(MSDS)

N-氧代煙酰胺價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2024/11/11XW19868183煙堿-N-氧化物
nicotinamide n-oxide;3-?pyridinecarboxamide;oxynicotinamide
1986-81-8100G648元
2024/11/11XW19868182煙堿-N-氧化物
nicotinamide n-oxide;3-?pyridinecarboxamide;oxynicotinamide
1986-81-825G184元
2024/11/11XW19868181煙堿-N-氧化物
nicotinamide n-oxide;3-?pyridinecarboxamide;oxynicotinamide
1986-81-85G42元

常見問題列表

生物活性
Nicotinamide N-oxide是生物體內(nèi)煙酰胺分解代謝物, 是高效選擇性的CXCR2受體拮抗劑。
靶點(diǎn)

CXCR2

Human Endogenous Metabolite

體外研究

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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