Candesartan Cilexetil
A prodrug of candesartan that is rapidly converted to the active drug after oral absorption. It is used to treat hypertension and heart failure with reduced ejection fraction. It offers the benefit of once-daily dosing for long-term cardiovascular protection.
分子量
610.7000 g/mol
LogP
7.00
TPSA
143.00 Ų
リピンスキーの五則
不適合
治療領域
作用機序
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.
2D構造
Cite this structure
Embed this structure
SMILES
CCOc1nc2cccc(C(=O)OC(C)OC(=O)OC3CCCCC3)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1
InChI
InChI=1S/C33H34N6O6/c1-3-42-32-34-28-15-9-14-27(31(40)43-21(2)44-33(41)45-24-10-5-4-6-11-24)29(28)39(32)20-22-16-18-23(19-17-22)25-12-7-8-13-26(25)30-35-37-38-36-30/h7-9,12-19,21,24H,3-6,10-11,20H2,1-2H3,(H,35,36,37,38)
Molecular Formula
C33H34N6O6
HBD / HBA
1 / 10
回転可能結合数
13
重原子数
45
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.
よくある質問
A prodrug of candesartan that is rapidly converted to the active drug after oral absorption. It is used to treat hypertension and heart failure with reduced ejection fraction. It offers the benefit of once-daily dosing for long-term cardiovascular protection.
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, Candesartan Cilexetil 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). CHEMBL1014. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 2540. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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