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178961-24-5

中文名稱 264W 94
CAS 178961-24-5
分子式 C23H31NO4S
分子量 417.56
MOL 文件 178961-24-5.mol
178961-24-5 結(jié)構(gòu)式 178961-24-5 結(jié)構(gòu)式

基本信息

英文別名
264W 94

常見(jiàn)問(wèn)題列表

生物活性
264W94 是有效的回腸膽汁酸轉(zhuǎn)運(yùn)蛋白 (IBAT) 抑制劑,是新型降膽固醇藥。264W94 具有 CYP7A1 誘導(dǎo)作用和抗血脂作用。
靶點(diǎn)

IBAT

體外研究

264W94 (0, 0.1, 0.25, 0.5 μM) inhibits human IBAT-specific transport of 5 μM TC by 14% to 75% in a concentration-dependent manner with IC 50 of 0.25 μM in CHO-hIBAT cells.

體內(nèi)研究

264W94 (orally; 0.03-1.0 mg/kg; twice a day for 3.5 days) dose-dependently attenuates diet-induced increases in serum LDL+VLDL-C, as well as the decrease in HDL-C.
264W94 (orally; 0.003, 0.01, 0.03, 0.1 mg/kg; twice a day for 2 days) increases fecal excretion of 75 SeHCAT in a dose-dependent manner.
264W94 (0.001, 0.01, 0.1, 1, and 10 mg/kg; twice a day for 2 weeks) reduces dose-dependently plasma glucose in male ZDF (ZDF/GmiCrl- fa/fa ) rats. Treatment of 264W94 prevents the decline of insulin dose-dependently without an increase in proinsulin levels.

Animal Model: Male Sprague Dawley rats (CD, Charles River, 270-310 gm)
Dosage: 0.03, 0.1, 0.3, 1.0 mg/kg
Administration: Orally; twice a day (9:00 am and 3:30 pm) for 3.5 days
Result: Dose-dependently attenuated diet-induced increases in serum LDL+VLDL-C, as well as the decrease in HDL-C.
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