三苯甲基坎地沙坦西来替昔酯
| CAS号 | 170791-09-0 | 货号 | BCP12026 |
| 中文名 | 三苯甲基坎地沙坦西来替昔酯 | ||
| 英文名 | Trityl candesartan cilexetil | ||
| 中文别名 | |||
| 英文别名 | |||
| 分子式 | C52H48N6O6 | 分子量 | 852.97 |
| 生物活性 | Candesartan cilexetil is a prodrug of the potent, long-acting, and selective angiotensin II type 1 receptor (AT1) antagonist, candesartan. It is rapidly hydrolyzed to candesartan during gastrointestinal absorptio. Candesartan blocks the vasoconstrictor and aldosterone-secreting effects of angiotensin II by selectively blocking the binding of angiotensin II to the AT1 receptor in many tissues, such as vascular smooth muscle and the adrenal gland. Its action is, therefore, independent of the pathways for angiotensin II synthesis. Candesartan has much greater affinity ( > 10,000-fold) for the AT1 receptor than for the AT2 receptor. | ||
| 信号通路 | GPCR/G Protein | ||
| 靶 点 | Angiotensin Receptor | ||
结构式
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