Structure via PubChem · Public domain (PubChem)
clevidipine
Sign in to saveAlso known as 4-(2,3-dichlorophenyl)-1,4-dihydro-2,6-dimethyl-3,5-Pyridinedicarboxylic acid methyl (1-oxobutoxy)methyl ester
Clevidipine (INN, trade name Cleviprex) is a dihydropyridine calcium channel blocker indicated for the reduction of blood pressure when oral therapy is not feasible or not desirable. Clevidipine is used IV only and practitioners titrate this drug to lower blood pressure. It has a half-life of approximately one minute. It is rapidly inactivated by esterases.
Chemical data
- Formula
- C21H23Cl2NO6
- Molecular weight
- 456.3 g/mol
- IUPAC name
- 5-O-(butanoyloxymethyl) 3-O-methyl 4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
- SMILES
- CCCC(=O)OCOC(=O)C1=C(NC(=C(C1C2=C(C(=CC=C2)Cl)Cl)C(=O)OC)C)C
- InChIKey
- KPBZROQVTHLCDU-UHFFFAOYSA-N
- XLogP
- 4.3
- Polar surface area
- 90.9 Ų
- H-bond donors
- 1
- H-bond acceptors
- 7
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Approved
- Molecule type
- Small molecule
- First approval
- 2008
- Admin. routes
- parenteral
- Indications
- hypertension, scoliosis, cardiovascular disease, vascular disease
via ChEMBL · EBI
Research
210 papers- Comparison of Clevidipine and Nicardipine for Acute Blood Pressure Reduction in Hemorrhagic Stroke.Neurocritical care · 2022
- The Current Role of Clevidipine in the Management of Hypertension.American journal of cardiovascular drugs : drugs, devices, and other interventions · 2022
- Clevidipine.Drugs in R&D · 2002
- Comparison between clevidipine and nicardipine in cerebrovascular diseases: A systematic review and meta-analysis.Clinical neurology and neurosurgery · 2023
- Clevidipine for the management of hypertension in the perioperative cardiac and noncardiac surgical settings: a systematic review.Frontiers in medicine · 2025
via PubMed
Wikidata facts
- Mass
- 455.090243
- Has use
- medication
Show 6 more facts
- chemical formula
- C₂₁H₂₃Cl₂NO₆
- World Health Organisation international non-proprietary name
- clevidipine
- canonical SMILES
- CCCC(=O)OCOC(=O)C1=C(NC(=C(C1C2=C(C(=CC=C2)Cl)Cl)C(=O)OC)C)C
- subject has role
- calcium channel blocker
- medical condition treated
- arterial hypertension
- Commons category
- Clevidipine
via Wikidata · CC0
~9 min read
Encyclopedic overview
10 sectionsContents
- Basic chemical and pharmacological properties
- Stereochemistry
- Dosage and administration
- Safety information
- Drug interactions
- Storage
- Phase III clinical trial results
- References
- Further reading
- External links
Clevidipine (INN, trade name Cleviprex) is a dihydropyridine calcium channel blocker indicated for the reduction of blood pressure when oral therapy is not feasible or not desirable. Clevidipine is used IV only and practitioners titrate this drug to lower blood pressure. It has a half-life of approximately one minute. It is rapidly inactivated by esterases.
It was approved by the United States Food and Drug Administration on August 1, 2008.
Excerpted from Wikipedia’s “clevidipine” article, available under the CC BY-SA 4.0 licence.