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Taribavirin hydrochloride is an orally active inosine monophosphate dehydrogenase inhibitor. Taribavirin hydrochloride is designed to concentrate within the liver to target HCV-infected hepatocytes while minimizing distribution within red blood cells and the development of hemolytic anemia [2].

Taribavirin hydrochloride is an orally active inosine monophosphate dehydrogenase inhibitor. Taribavirin hydrochloride is designed to concentrate within the liver to target HCV-infected hepatocytes while minimizing distribution within red blood cells and the development of hemolytic anemia [2].
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 2 mg | ¥ 1,280 | 5日内发货 | |
| 5 mg | ¥ 2,160 | 5日内发货 | |
| 25 mg | ¥ 7,690 | 6-8周 | |
| 50 mg | ¥ 9,990 | 6-8周 | |
| 100 mg | ¥ 15,500 | 6-8周 |
| 产品描述 | Taribavirin hydrochloride is an orally active inosine monophosphate dehydrogenase inhibitor. Taribavirin hydrochloride is designed to concentrate within the liver to target HCV-infected hepatocytes while minimizing distribution within red blood cells and the development of hemolytic anemia [2]. |
| 体外活性 | Taribavirin hydrochloride (0-2 μM; 24 hours) obviously induces MCF-7 cell death. It recording half inhibitory effect (IC50) of 0.756 μM in MCF-7 cells [1]. |
| 分子量 | 279.68 |
| 分子式 | C8H14ClN5O4 |
| CAS No. | 40372-00-7 |
| Smiles | Cl.NC(=N)c1ncn(n1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O |
| 密度 | no data available |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
对于不同动物的给药剂量换算,您也可以参考 更多