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TGR5 Receptor Agonist 3
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
TGR5 Receptor Agonist 3图片
CAS NO:2643391-08-4
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
TGR5 Receptor Agonist 3 (Compound 19) 是 G 蛋白偶联胆汁酸受体 1(GPBAR1,TGR5)激动剂软药化合物,具有降低胆囊充盈效果(良好的胆囊安全性),对 hTGR5 和 mTGR5 的EC50分别为 16.4 和 209 nM。
生物活性

TGR5 Receptor Agonist 3 (Compound 19) is a soft-drug G-protein-coupled bile acid receptor 1 (GPBAR1, TGR5) agonist with reduced gallbladder-filling effects (favorable gallbladder safety), withEC50s of 16.4 and 209 nM for hTGR5 and mTGR5, respectively[1].

体外研究
(In Vitro)

TGR5 Receptor Agonist 3 (compound 19) (10-50μM, 2 hours) activates TGR5 in fetal rat intestinal cells (FRIC) and NCI-H716 cells to promote GLP-1 secretion in a dose-dependent manner[1].

体内研究
(In Vivo)

TGR5 Receptor Agonist 3 (compound 19) has good targeting and can effectively activate TGR5, thus promoting the secretion of GLP-1 in plasma and regulating the homeostasis of glucose metabolism in male ICR mice[1].
TGR5 Receptor Agonist 3 (compound 19) can be rapidly absorbed and metabolized in male ICR mice, and has a good safety profile[1].
TGR5 Receptor Agonist 3 (compound 19) (oral gavage; 50 mg/kg; one hour) can be gavaged into overnight-fasted male ICR mice for one hour with a Cmaxvalue of 0.003 μg/mL[1].
TGR5 Receptor Agonist 3 (compound 19) can reduce gallbladder-filling and safety in vivo[1].

分子量

513.54

Formula

C29H27N3O6

CAS 号

2643391-08-4

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.