Amlodipine Benzoate
The benzoate salt form of amlodipine, a calcium channel blocker used to lower blood pressure by relaxing and widening blood vessels. It provides the same therapeutic effects as other amlodipine salts in treating hypertension.
Peso Molecular
531,0000 g/mol
TPSA
137,00 Ų
Áreas Terapêuticas
Mecanismo de Ação
Blocks L-type voltage-gated calcium channels in vascular smooth muscle and cardiac myocytes, reducing calcium influx during depolarization. This produces vasodilation, decreased myocardial contractility, and reduced heart rate.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Blocks L-type voltage-gated calcium channels in vascular smooth muscle and cardiac myocytes, reducing calcium influx during depolarization. This produces vasodilation, decreased myocardial contractility, and reduced heart rate.
Estrutura 2D
Cite this structure
Embed this structure
SMILES
CCOC(=O)C1=C(COCCN)NC(C)=C(C(=O)OC)C1c1ccccc1Cl.O=C(O)c1ccccc1
InChI
InChI=1S/C20H25ClN2O5.C7H6O2/c1-4-28-20(25)18-15(11-27-10-9-22)23-12(2)16(19(24)26-3)17(18)13-7-5-6-8-14(13)21;8-7(9)6-4-2-1-3-5-6/h5-8,17,23H,4,9-11,22H2,1-3H3;1-5H,(H,8,9)
Molecular Formula
C27H31ClN2O7
HBD / HBA
3 / 9
Ligações Rotacionáveis
11
Átomos Pesados
37
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.
Perguntas frequentes
The benzoate salt form of amlodipine, a calcium channel blocker used to lower blood pressure by relaxing and widening blood vessels. It provides the same therapeutic effects as other amlodipine salts in treating hypertension.
Blocks L-type voltage-gated calcium channels in vascular smooth muscle and cardiac myocytes, reducing calcium influx during depolarization. This produces vasodilation, decreased myocardial contractility, and reduced heart rate.
Yes, Amlodipine Benzoate 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). CHEMBL4594262. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 44481893. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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