Tenapanor(AZD1722RDX5791)
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。
产品介绍
CAS: | 1234423-95-0 |
分子式: | C50H66Cl4N8O10S2 |
分子量: | 1145.05 |
纯度: | >98% |
溶解性: | DMSO |
存储: | Powder -20℃ 3 years; 4℃ 2 years In solvent -80℃ 6 months;-20℃ 1 month |
研究领域: | Cardiovascular Disease |
Target: | IC50: 5 nM (NHE3, human), 10 nM (NHE3, rat)[1] |
描述: | Tenapanor is an inhibitor of the Na+/H+ exchanger NHE3 with IC50 values of 5 and 10 nM against human and Rat NHE3, respectively. |