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Tenapanor (RDX 5791) 是钠氢离子交换NHE3的有效抑制剂, 对人和大鼠NHE3的IC50分别是5和10 nM。
Tenapanor (RDX 5791) 是钠氢离子交换NHE3的有效抑制剂, 对人和大鼠NHE3的IC50分别是5和10 nM。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 313 | 现货 | |
5 mg | ¥ 747 | 现货 | |
10 mg | ¥ 1,180 | 现货 | |
25 mg | ¥ 2,490 | 现货 | |
50 mg | ¥ 3,890 | 现货 | |
100 mg | ¥ 5,680 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 3,970 | 现货 |
产品描述 | Tenapanor (RDX 5791) is an inhibitor of the sodium-proton (Na(+)/H(+)) exchanger NHE3, which plays a prominent role in sodium handling in the gastrointestinal tract and kidney. Tenapanor possesses an excellent preclinical safety profile and, as of now, there are no serious concerns about its side effects. |
靶点活性 | NHE3 (rat):10 nM (IC50), NHE3 (human):5 nM (IC50) |
别名 | Tenapanor free base, RDX-5791, RDX5791, RDX 5791, AZD-1722, AZD1722, AZD 1722 |
分子量 | 1145.05 |
分子式 | C50H66Cl4N8O10S2 |
CAS No. | 1234423-95-0 |
Smiles | CN1C[C@@H](c2cccc(c2)S(=O)(=O)NCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCNS(=O)(=O)c2cccc(c2)[C@@H]2CN(C)Cc3c(Cl)cc(Cl)cc23)c2cc(Cl)cc(Cl)c2C1 |
密度 | no data available |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||
溶解度信息 | DMSO: 50 mg/mL (43.67 mM), Sonication is recommended. H2O: < 0.1 mg/mL (insoluble) | |||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||
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