Azilsartan Medoxomil
A prodrug of azilsartan, an angiotensin II type 1 receptor blocker that effectively lowers blood pressure by blocking vasoconstriction and aldosterone secretion. Studies suggest it may provide particularly effective 24-hour blood pressure control.
الوزن الجزيئي
568,5000 g/mol
LogP
4,90
TPSA
140,00 Ų
قاعدة ليبينسكي للخمسة
ناجح
المجالات العلاجية
آلية العمل
Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.
البنية ثنائية الأبعاد
Cite this structure
Embed this structure
SMILES
CCOc1nc2cccc(C(=O)OCc3oc(=O)oc3C)c2n1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1
InChI
InChI=1S/C30H24N4O8/c1-3-38-28-31-23-10-6-9-22(27(35)39-16-24-17(2)40-30(37)41-24)25(23)34(28)15-18-11-13-19(14-12-18)20-7-4-5-8-21(20)26-32-29(36)42-33-26/h4-14H,3,15-16H2,1-2H3,(H,32,33,36)
Molecular Formula
C30H24N4O8
HBD / HBA
1 / 10
الروابط القابلة للدوران
10
الذرات الثقيلة
42
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
الأسئلة الشائعة
A prodrug of azilsartan, an angiotensin II type 1 receptor blocker that effectively lowers blood pressure by blocking vasoconstriction and aldosterone secretion. Studies suggest it may provide particularly effective 24-hour blood pressure control.
Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.
Yes, Azilsartan Medoxomil is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL2028661. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 135409642. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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