GPR40 agonist 6,99.64%
产品编号:Bellancom-147351| CAS NO:1798751-25-3| 分子式:C20H19NO4| 分子量:337.37
本网站销售的所有产品仅用于工业应用或者科学研究等非医疗目的,不可用于人类或动物的临床诊断或者治疗,非药用,非食用,
GPR40 agonist 6
产品介绍 | GPR40 agonist 6 (Compound 7a) 是一种有效的、选择性的游离脂肪酸受体 1 (FFAR1 或 GPR40) 激动剂,EC50 为 0.058 μM。 | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
生物活性 | GPR40 agonist 6 (Compound 7a) is a potent and selective free fatty acid receptor 1 (FFAR1 or GPR40) agonist with an EC50 of 0.058 μM. | ||||||||||||||||
体外研究 |
GPR40 agonist 6 (Compound 7a) shows a very favorable ADME profile, and shows no significant inhibition of the principal cytochrome P450 isoforms (1A2, 2C9, 2C19, 2D6 and 3A4) at 5 µM.
aEach value is an average of n = 4, measured at c = 1 µM. bEach value is an average of n = 2. cEach value is an average of n = 5, measured at c = 2 µM. dEach value is an average of n = 2, measured at c = 10 µM. 西域 has not independently confirmed the accuracy of these methods. They are for reference only. | ||||||||||||||||
体内研究 | |||||||||||||||||
体内研究 | |||||||||||||||||
性状 | Solid | ||||||||||||||||
溶解性数据 |
In Vitro:
DMSO : 125 mg/mL (370.51 mM; Need ultrasonic) 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。 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
| ||||||||||||||||
参考文献 |