CAS NO: | 1345982-69-5 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
1mg | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
生物活性 | Linerixibat (GSK2330672) is a highly potent, nonabsorbable and orally activeapical sodium-dependent bile acid transporter(ASBT)inhibitor with anIC50of 42 nMhuman ASBT. Linerixibat can be used as lipid-lowering agent. Linerixibat has the potential for type 2 diabetes and Primary Biliary Cholangitis treatment[1][2][3]. | ||||||||||||||||
IC50& Target | IC50: 42 nM (Apical sodium-dependent bile acid transporter (ASBT))[1] | ||||||||||||||||
体外研究 (In Vitro) | The zwitterionic, nonhygroscopic, crystalline salt form of Linerixibat (Compound 56) shows good aqueous solubility at pH 7.4 (>7 mg/mL), excellent thermal stability, and did not generate reactive or humanspecific metabolite, characteristics[1]. | ||||||||||||||||
体内研究 (In Vivo) | Linerixibat (GSK2330672; 0.05-10 mg/kg; oral gavage; twice daily; for 14 days; male ZDF rat) treatment lowers glucose in an animal model of type 2 diabetes[1].
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Clinical Trial | |||||||||||||||||
分子量 | 546.68 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C28H38N2O7S | ||||||||||||||||
CAS 号 | 1345982-69-5 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 50 mg/mL(91.46 mM;Need ultrasonic) 配制储备液
* 请根据半岛bd体育手机客户端
在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的半岛bd体育手机客户端
失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
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