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133208-93-2

中文名稱 NO-1886
英文名稱 NO-1886
CAS 133208-93-2
分子式 C19H20BrN2O4P
分子量 451.25
MOL 文件 133208-93-2.mol
更新日期 2026/05/25 13:08:18
133208-93-2 結(jié)構(gòu)式 133208-93-2 結(jié)構(gòu)式

基本信息

中文別名
化合物NO-1886
4-((4-溴-2-氰基苯基)氨基甲酰基)芐基膦酸二乙酯
英文別名
NO-1886
OPF 009
ibrolipim
Ibrolipim NO-1886
Lipoprotein Lipase Activator
4-diethoxyphosphorylmethyl-N-(4-bromo-2-cyanophenyl)benzamide
Diethyl 4-[(4-bromo-2-cyanophenyl)carbamoyl]benzylphosphonate
N-(4-bromo-2-cyanophenyl)-4-(diethoxyphosphorylmethyl)benzamide
Diethyl 4-[(4-bromo-2-cyanophenyl)carbamoyl]benzylphosphonate, Ibrolipim, OPF 009
Phosphonic acid, [[4-[[(4-bromo-2-cyanophenyl)amino]carbonyl]phenyl]methyl]-, diethyl ester

物理化學(xué)性質(zhì)

熔點(diǎn)160.5-162.1 °C
沸點(diǎn)512.5±50.0 °C(Predicted)
密度1.44±0.1 g/cm3(Predicted)
儲存條件Sealed in dry,2-8°C
溶解度二甲基亞砜:≥20mg/mL
酸度系數(shù)(pKa)11.51±0.70(Predicted)
形態(tài)粉末
顏色灰白色至淡黃色
InChI1S/C19H20BrN2O4P/c1-3-25-27(24,26-4-2)13-14-5-7-15(8-6-14)19(23)22-18-10-9-17(20)11-16(18)12-21/h5-11H,3-4,13H2,1-2H3,(H,22,23)
InChIKeyKPRTURMJVWXURQ-UHFFFAOYSA-N
SMILESCCOP(=O)(Cc1ccc(cc1)C(=O)Nc2ccc(Br)cc2C#N)OCC

安全數(shù)據(jù)

危險(xiǎn)性符號(GHS)有毒 (GHS06)
GHS06
警示詞危險(xiǎn)
危險(xiǎn)性描述H301
防范說明P301+P310
危險(xiǎn)品標(biāo)志Xi,T
危險(xiǎn)類別碼36/37/38-25
安全說明26-36-45
危險(xiǎn)品運(yùn)輸編號UN 2811 6.1 / PGIII
WGK Germany3
存儲類別6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
危險(xiǎn)性類別Acute Tox. 3 Oral

圖譜信息

NO-1886價(jià)格(試劑級)
報(bào)價(jià)日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價(jià)格
2026/03/03S0536NO-1886
Ibrolipim
133208-93-25mg2678.13元
2026/03/03S0536NO-1886
Ibrolipim
133208-93-225mg8099.91元
2025/12/22HY-117549Ibrolipim133208-93-21 mg200元

常見問題列表

生物活性
Ibrolipim (NO-1886) 是一種口服活性的脂蛋白脂肪酶 (LPL) 激活劑。 Ibrolipim 可降低血漿甘油三酸酯,增加高密度脂蛋白膽固醇水平。 Ibrolipim 具有腎保護(hù)和降血脂的作用。
靶點(diǎn)

Lipoprotein lipase (LPL)

體外研究

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.
體內(nèi)研究

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.
"133208-93-2" 相關(guān)產(chǎn)品信息
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