Ranitidine 是一种有效的，选择性的，具有口服活性的组胺 H2 受体 (histamine H2-receptor) 拮抗剂，IC50为 3.3 μM，可抑制胃液分泌。Ranitidine 还一种是CYP2C19和CYP2C9的弱抑制剂。
| 生物活性 | Ranitidine is a potent, selective and orally activehistamine H2-receptorantagonist with anIC50of 3.3 μM that inhibits gastric secretion. Ranitidine is a weak inhibitor ofCYP2C19andCYP2C9[1][2]. |
| IC50& Target[1][2] | H2Receptor 3.3 μM (IC50) | CYP2C19 | CYP2C9 |
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| 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. |
