产品描述
| 熔点 | 225-230 °C |
| 溶解性 | Soluble in DMSO (90 mg/mL at 25 °C), water (<1 mg/mL at 25 °C), and ethanol (6 mg/mL at 25 °C). |
| 存贮条件 | 储存温度 2-8°C |
| 应用 | A selective vasopressin receptor 2 antagonist. |
| 产品介绍 | Tolvaptan是一种选择性，竞争性的精氨酸加压素受体2拮抗剂，抑制AVP-诱导的血小板聚集，IC50为1.28μM。 |
| 备注 | Tolvaptan is a selective, competitive arginine vasopressin receptor 2 antagonist with an IC50 of 1.28μM for the inhibition of AVP-induced platelet aggregation. |
| 生化机理 | Tolvaptan is a selective, competitive AVP Receptor V2 antagonist with an IC50 of 1.28μM for the inhibition of AVP-induced platelet aggregation. Tolvaptan is used to treat hyponatremia associated with congestive heart failure, cirrhosis, and the syndrome of inappropriate antidiuretic hormone. Tolvaptan is also in fast-track clinical trials for polycystic kidney disease. Treatment with Tolvaptan causes rapid and sustained body weight reductions concurrent with increases in urine output, improves and/or normalizes serum sodium in hyponatremic patients, reduces signs and symptoms of congestion and increases thirst. However, Tolvaptan has not been shown to decrease heart failure re-hospitalization or mortality. As an adjunct to standard therapy, Tolvaptan is unique in that it is virtually the only novel agent tested in patients hospitalized for acute heart failure syndrome to reach its primary end point for short-term efficacy without causing deleterious side effects. |
| 别名 | 托伐普坦; N-[4-[(7-氯-5-羟基-2,3,4,5-四氢-1-苯并氮杂卓-1-甲酰基]-3-甲基苯基]-2-甲基苯甲酰胺;N-[4-[(7-Chloro-2,3,4,5-tetrahydro-5-hydroxy-1H-1-benzazepin-1-yl)carbonyl]-3-methylphenyl]-2-methylbenzamide;OPC 41061; Samsca; OPC-41061 |
