Clevidipine
A short-acting calcium channel blocker given intravenously to rapidly lower dangerously high blood pressure, particularly in surgical or critical-care settings. It works by relaxing the muscles in artery walls to reduce vascular resistance.
Khối lượng phân tử
456,3000 g/mol
LogP
4,30
TPSA
90,90 Ų
Lipinski RO5
Đạt
Lĩnh vực điều trị
Cơ chế tác dụng
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.
Cấu trúc 2D
Cite this structure
Embed this structure
SMILES
CCCC(=O)OCOC(=O)C1=C(C)NC(C)=C(C(=O)OC)C1c1cccc(Cl)c1Cl
InChI
InChI=1S/C21H23Cl2NO6/c1-5-7-15(25)29-10-30-21(27)17-12(3)24-11(2)16(20(26)28-4)18(17)13-8-6-9-14(22)19(13)23/h6,8-9,18,24H,5,7,10H2,1-4H3
Molecular Formula
C21H23Cl2NO6
HBD / HBA
1 / 7
Liên kết có thể quay
10
Nguyên tử nặng
30
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.
Câu hỏi thường gặp
A short-acting calcium channel blocker given intravenously to rapidly lower dangerously high blood pressure, particularly in surgical or critical-care settings. It works by relaxing the muscles in artery walls to reduce vascular resistance.
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, Clevidipine 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). CHEMBL1237132. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 153994. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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