- ￥2660 - 3432
- MedChemExpress(MCE)
- 美国
- HY-16278
- 2025年12月05日
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- 详细信息
- 技术资料
- 保存条件：
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 英文名：
LCQ-908
- 库存：
货期：1-2天
- 供应商：
MedChemExpress LLC
- 规格：
10 mM * 1 mL/5 mg/10 mg
| 规格： | 10 mM * 1 mL | 产品价格： | ￥2926.0 |
|---|---|---|---|
| 规格： | 5 mg | 产品价格： | ￥2660.0 |
| 规格： | 10 mg | 产品价格： | ￥3432.0 |
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Pradigastat
CAS No. : 956136-95-1
MCE 国际站：Pradigastat
产品活性：Pradigastat (LCQ-908) 是一种有效的，选择性的，口服活性的二酰基甘油酰基转移酶 1 (DGAT1) 抑制剂。Pradigastat 具有抗肥胖和抗糖尿病作用。
研究领域：Metabolic Enzyme/Protease
作用靶点：Acyltransferase
In Vitro: Pradigastat inhibits breast cancer resistance protein (BCRP)-mediated efflux activity in a dose-dependent fashion in a BCRP over-expressing human ovarian cancer cell line with an IC50 value of 5 μM. Pradigastat inhibits OATP1B1, OATP1B3, and OAT3 activity in a concentration-dependent manner with estimated IC50 values of 1.66 μM, 3.34 μM, and 0.973 μM, respectively.
In Vivo: Pradigastat (LCQ-908) inhibits the postprandial triglyceride levels in rats, dogs and monkeys. In rats whose lipoprotein lipase (LPL) activity has been abolished, Pradigastat reduces the postprandial accumulation of plasma triglyceride. Pradigastat decreases the postprandial rate of chylomicron triglyceride (CM-TG) secretion into the lymphatic duct and reduces the size of chylomicrons.
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