Amlodipine

CHEMBL1491 Phase 4 Approuvé Small molecule
Half-Life
30-50 hours
Bioavailability
Protein Binding
Molecular Weight
408.9 g/mol
LogP
3.0
Phase
4

This calcium channel blocker relaxes the walls of blood vessels, making it easier for the heart to pump blood and lowering blood pressure. It is prescribed for hypertension and chest pain, and some research suggests potential roles in neurological and heart rhythm conditions.

Masse moléculaire

408,8800 g/mol

LogP

3,00

TPSA

99,90 Ų

Règle des 5 de Lipinski

Conforme

Aires thérapeutiques

Classes de médicaments

Mécanisme d'action

Dihydropyridine calcium channel blocker.

Pharmacokinetics (PK)

Half-Life 30-50 hours

Pharmacodynamics (PD)

Mécanisme

Dihydropyridine calcium channel blocker.

Structure 2D

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SMILES

CCOC(=O)C1=C(COCCN)NC(C)=C(C(=O)OC)C1c1ccccc1Cl

InChI

InChI=1S/C20H25ClN2O5/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/h5-8,17,23H,4,9-11,22H2,1-3H3

Molecular Formula

C20H25ClN2O5

HBD / HBA

2 / 7

Liaisons Rotatives

10

Atomes Lourds

28

No side effects recorded

Side effect data is not yet available for this drug.

Foire aux questions

This calcium channel blocker relaxes the walls of blood vessels, making it easier for the heart to pump blood and lowering blood pressure. It is prescribed for hypertension and chest pain, and some research suggests potential roles in neurological and heart rhythm conditions.

Dihydropyridine calcium channel blocker.

Key pharmacokinetic parameters for Amlodipine: Half-life: 30-50 hours.

Yes, Amlodipine is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

Related Drugs

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References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1491. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 2162. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Avertissement médical

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.