Name | pratosartan |
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Synonyms |
Pratosartan (JAN/INN)
UNII-66VLQ6E6DL 2-propyl-3-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]-5,6,7,8-tetrahydrocyclohepta[d]imidazol-4-one KD 3-671 KT3-671 Pratosartan |
Description | Pratosartan is a selective angiotensin II receptor antagonist. |
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Related Catalog | |
Target |
angiotensin II receptor[1] |
In Vitro | Pratosartan, which is an orally active angiotensin II (AII) antagonist, exhibiting selective and potent antagonistic activity to AT1 subtype[1]. Pratosartan is a new angiotensin II type 1 receptor blocker. Pratosartan is an effective and well tolerated antihypertensive drug, and may has beneficial effect on hypertensive patients with some metabolic disorders[2]. |
References |
Density | 1.321g/cm3 |
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Boiling Point | 692.92ºC at 760 mmHg |
Molecular Formula | C25H26N6O |
Molecular Weight | 426.51400 |
Flash Point | 372.864ºC |
Exact Mass | 426.21700 |
PSA | 89.35000 |
LogP | 4.64010 |
Vapour Pressure | 0mmHg at 25°C |
Index of Refraction | 1.701 |
Storage condition | 2-8℃ |