NO-1886

NO-1886

中文名称NO-1886
中文同义词4-((4-溴-2-氰基苯基)氨基甲酰基)苄基膦酸二乙酯;化合物NO-1886
英文名称NO-1886
英文同义词OPF 009;Lipoprotein Lipase Activator;NO-1886;Diethyl 4-[(4-bromo-2-cyanophenyl)carbamoyl]benzylphosphonate;4-diethoxyphosphorylmethyl-N-(4-bromo-2-cyanophenyl)benzamide;ibrolipim;Diethyl 4-[(4-bromo-2-cyanophenyl)carbamoyl]benzylphosphonate, Ibrolipim, OPF 009;Ibrolipim NO-1886
CAS号133208-93-2
分子式C19H20BrN2O4P
分子量451.25
EINECS号
相关类别
Mol文件133208-93-2.mol
结构式NO-1886 结构式

NO-1886 性质

熔点160.5-162.1 °C
沸点512.5±50.0 °C(Predicted)
密度1.44±0.1 g/cm3(Predicted)
储存条件Sealed in dry,2-8°C
溶解度二甲基亚砜:≥20mg/mL
形态粉末
酸度系数(pKa)11.51±0.70(Predicted)
颜色灰白色至浅黄色

NO-1886 用途与合成方法

Ibrolipim (NO-1886) 是一种口服活性的脂蛋白脂肪酶 (LPL) 激活剂。 Ibrolipim 可降低血浆甘油三酸酯,增加高密度脂蛋白胆固醇水平。 Ibrolipim 具有肾保护和降血脂的作用。

Lipoprotein lipase (LPL)

Ibrolipim (0.5-10 μM; 0-24 hours; THP-1 macrophage-derived foam cells) treatment increases ABCA1 and ABCG1 expression at translational levels in a dose-dependent and time-dependent manner .
Ibrolipim (0.5-10 μM; 0-24 hours; THP-1 macrophage-derived foam cells) treatment increases ABCA1 and ABCG1 expression at the transcriptional levels in a dose-dependent and time-dependent manner .
Ibrolipim 5 and 50 μmol/L significantly increases cholesterol efflux from THP-1 macrophage-derived foam cells to apoA-I or HDL. LXRα is also upregulated by the Ibrolipim treatment. LXRα small interfering RNA completely abolishes the promotion effect that is induced by Ibrolipim.

Western Blot Analysis

Cell Line: THP-1 macrophage-derived foam cells
Concentration: 0.5 μM, 5 μM, 10 μM
Incubation Time: 0 hour, 6 hours, 12 hours, 24 hours
Result: Increased ABCA1 and ABCG1 translational levels in a dose-dependent and time-dependent manner.

RT-PCR

Cell Line: THP-1 macrophage-derived foam cells
Concentration: 0.5 μM, 5 μM, 10 μM
Incubation Time: 0 hour, 6 hours, 12 hours, 24 hours
Result: Increased ABCA1 and ABCG1 expression at the transcriptional levels in a dose-dependent and time-dependent manner.

Ibrolipim (NO-1886; 100 mg/kg; oral administration; daily; for 8 weeks; female Sprague-Dawley rats) treatment decreases accumulation of visceral fat and suppresses the increase in body weight resulting from the ovariectomy. Ibrolipim decreases the respiratory quotient and increases expression of the fatty acid translocase messenger RNA (mRNA) in the liver, soleus muscle, and mesenteric fat. Ibrolipim also increases the expression of fatty acid-binding protein mRNA in the liver and soleus muscle and the expression of the uncoupling protein 3 (UCP3) mRNA in the heart, soleus muscle, and mesenteric fat, but not in the brown adipose tissue.

Animal Model: Female Sprague-Dawley rats (10-week-old; 200-260 g) with experimental ovariectomy treatment
Dosage: 100 mg/kg
Administration: Oral administration; daily; for 8 weeks
Result: Decreased accumulation of visceral fat and suppressed the increase in body weight resulting from the ovariectomy.

安全信息

危险品标志Xi,T
危险类别码36/37/38-25
安全说明26-36-45
危险品运输编号UN 2811 6.1 / PGIII
WGK Germany3

MSDS信息

更新日期产品编号产品名称CAS号包装价格
2024/04/30HY-117549Ibrolipim1 mg200元
2024/04/30HY-117549NO-1886
Ibrolipim
133208-93-25mg400元

NO-1886 上下游产品信息

"NO-1886"相关产品信息
间溴苯甲腈 4-甲基苄基膦酸二乙酯 2-氨基-5-溴苯甲腈
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