Benazepril Hydrochloride
The hydrochloride salt of benazepril, the standard commercial formulation of this ACE inhibitor for treating hypertension and heart failure. It also provides kidney-protective effects in diabetic kidney disease.
Berat Molekul
460,9000 g/mol
TPSA
95,90 Ų
Area Terapeutik
Mekanisme Kerja
Inhibits angiotensin-converting enzyme (ACE), preventing the conversion of angiotensin I to angiotensin II, a potent vasoconstrictor. This reduces peripheral vascular resistance, decreases aldosterone secretion, and lowers blood pressure.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Inhibits angiotensin-converting enzyme (ACE), preventing the conversion of angiotensin I to angiotensin II, a potent vasoconstrictor. This reduces peripheral vascular resistance, decreases aldosterone secretion, and lowers blood pressure.
Struktur 2D
Cite this structure
Embed this structure
SMILES
CCOC(=O)[C@H](CCc1ccccc1)N[C@H]1CCc2ccccc2N(CC(=O)O)C1=O.Cl
InChI
InChI=1S/C24H28N2O5.ClH/c1-2-31-24(30)20(14-12-17-8-4-3-5-9-17)25-19-15-13-18-10-6-7-11-21(18)26(23(19)29)16-22(27)28;/h3-11,19-20,25H,2,12-16H2,1H3,(H,27,28);1H/t19-,20-;/m0./s1
Molecular Formula
C24H29ClN2O5
HBD / HBA
3 / 6
Ikatan yang Dapat Dirotasi
10
Atom Berat
32
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.
Pertanyaan yang Sering Diajukan
The hydrochloride salt of benazepril, the standard commercial formulation of this ACE inhibitor for treating hypertension and heart failure. It also provides kidney-protective effects in diabetic kidney disease.
Inhibits angiotensin-converting enzyme (ACE), preventing the conversion of angiotensin I to angiotensin II, a potent vasoconstrictor. This reduces peripheral vascular resistance, decreases aldosterone secretion, and lowers blood pressure.
Yes, Benazepril Hydrochloride 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). CHEMBL1694. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 5362123. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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