Cobicistat (GS-9350) is a potent and selective inhibitor of CYP3A with IC50 of 30-285 nM.
Cobicistat (GS-9350) is a potent and selective inhibitor of CYP3A with IC50 of 30-285 nM.
动物 A (mg/kg) = 动物 B (mg/kg)×动物 B的Km系数/动物 A的Km系数 | |
例如,已知某工具药用于小鼠的剂量为88 mg/kg , 则用于大鼠的剂量换算方法:将88 mg/kg 乘以小鼠的Km系数(3),再除以大鼠的Km系数(6),得到该药物用于大鼠的等效剂量44 mg/kg。
[1] Mari Shiomi,et al. Effects of a protein-rich drink or a standard meal on the pharmacokinetics of elvitegravir, cobicistat, emtricitabine and tenofovir in healthy Japanese male subjects: A randomized, three-way crossover study. J Clin Pharmacol. 2014 Jun; 54(6): 640–648. Published online 2014 Mar 18. doi: 10.1002/jcph.283.
[2] Chinnalalaiah Runja,et al. A Validated Stability Indicating RP-HPLC Method for the Determination of Emtricitabine, Tenofovir Disoproxil Fumarate, Elvitegravir and Cobicistat in Pharmaceutical Dosage Form. J Chromatogr Sci. 2016 May; 54(5): 759–764. Published online 2016 Feb 9. doi: 10.1093/chromsci/bmw004.
分子式 C40H53N7O5S2 |
分子量 776.02 |
CAS号 1004316-88-4 |
储存方式 -20 ℃长期冷藏储存。冰袋运输 |
溶剂(常温) |
DMSO 100 mg/mL |
Water <1 mg/mL |
Ethanol 100 mg/mL |
体内溶解度
5% DMSO+40% PEG 300+ddH2O 10mg/mL
注:以上所有数据均来自公开文献,并不保证对所有实验均有效,数据仅供参考。
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