Levamlodipine
This is the pharmacologically active form (S-enantiomer) of amlodipine, a calcium channel blocker used to treat high blood pressure and angina by relaxing blood vessel walls. Using the single active enantiomer may allow for effective treatment at lower doses compared to the racemic mixture.
分子量
408.9000 g/mol
LogP
3.00
TPSA
99.90 Ų
Lipinski 五规则
符合
治疗领域
作用机制
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.
二维结构
Cite this structure
Embed this structure
SMILES
CCOC(=O)C1=C(COCCN)NC(C)=C(C(=O)OC)[C@@H]1c1ccccc1Cl
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/t17-/m0/s1
Molecular Formula
C20H25ClN2O5
HBD / HBA
2 / 7
可旋转键数
10
重原子数
28
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.
常见问题
This is the pharmacologically active form (S-enantiomer) of amlodipine, a calcium channel blocker used to treat high blood pressure and angina by relaxing blood vessel walls. Using the single active enantiomer may allow for effective treatment at lower doses compared to the racemic mixture.
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, Levamlodipine 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). CHEMBL2111097. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 9822750. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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