CAS NO: | 447410-57-3 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | SB756050 is a selectiveTGR5agonist. SB756050 has the potential for type 2 diabetes treatment. | ||||||||||||||||
体外研究 (In Vitro) | TGR5 is a bile acid receptor and a potential target for the treatment of type 2 diabetes (T2D)[1]. | ||||||||||||||||
体内研究 (In Vivo) | SB756050 is well‐ olerated; it is readily absorbed, exhibited nonlinear pharmacokinetics with a less than dose‐proportional increase in plasma exposure above 100 mg, and demonstrates no significant changes in exposure when co‐administered with sitagliptin. SB756050 demonstrates highly variable pharmacodynamic effects both within dose groups and between doses, with increases in glucose seen at the two lowest doses and no reduction in glucose seen at the two highest doses. The glucose effects of SB756050 sitagliptin are comparable to those of sitagliptin alone, even though gut hormone plasma profiles are different[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 500.59 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C21H28N2O8S2 | ||||||||||||||||
CAS 号 | 447410-57-3 | ||||||||||||||||
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 : ≥ 150 mg/mL(299.65 mM) *"≥" means soluble, but saturation unknown. 配制储备液
* 请根据产品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产品失效。 |