Clevidipine
Dihydropyridine Calcium Channel Blocker — CARDIOVASCULAR SYSTEM
Also known as: clevelox, cleviprex
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Clevidipine is an ofp drug in the Dihydropyridine Calcium Channel Blocker class catalogued in DrugCentral. It was first approved by the FDA in 2008. Its mechanism of action is classified as Calcium Channel Antagonists. DrugCentral lists 2 molecular targets, including CACNA1C and CACNA1D. Recorded indications include Hypertensive disorder.
- Approval status: ofp (first approved 2008 by the FDA).
- Drug class: Dihydropyridine Calcium Channel Blocker.
- Mechanism of action: Calcium Channel Antagonists.
- Molecular targets: CACNA1C and CACNA1D (2 listed in DrugCentral).
- Indications: Hypertensive disorder.
- ATC code: C08CA16 (Dihydropyridine derivatives).
- Molecular formula: C21H23Cl2NO6; molecular weight 456.32 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Hypertensive disorder
Contraindications (7)
- Heart failure
- Hypertriglyceridemia
- Low blood pressure
- Minimal change disease
- Pancreatitis
- Severe Aortic Valve Stenosis
- Tachyarrhythmia
Mechanism & targets
| Mechanism of action (MoA) | Calcium Channel Antagonists |
|---|---|
| Established pharmacologic class | Dihydropyridine Calcium Channel Blocker |
Molecular targets (2)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Voltage-dependent L-type calcium channel subunit alpha-1C | CACNA1C | blocker | — |
| Voltage-dependent L-type calcium channel subunit alpha-1D | CACNA1D | blocker | — |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2008-08-01 | FDA | — | MEDICINES CO |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
C08CA16 | CARDIOVASCULAR SYSTEM › CALCIUM CHANNEL BLOCKERS › SELECTIVE CALCIUM CHANNEL BLOCKERS WITH MAINLY VASCULAR EFFECTS › Dihydropyridine derivatives |
Reported adverse-event signals
Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.
| MedDRA term | LLR |
|---|---|
| Ventilation perfusion mismatch | 186.9 |
Chemical structure
| Molecular formula | C21H23Cl2NO6 |
|---|---|
| Molecular weight | 456.32 g/mol |
| CAS number | 167221-71-8 |
| InChIKey | KPBZROQVTHLCDU-UHFFFAOYSA-N |
| PubChem CID | 153994 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Clevidipine used for?
DrugCentral lists the following indications for Clevidipine: Hypertensive disorder.
How does Clevidipine work?
Clevidipine is classified as Calcium Channel Antagonists; its molecular targets in DrugCentral include CACNA1C (blocker) and CACNA1D (blocker).
When was Clevidipine first approved?
Clevidipine was first approved by the FDA in 2008.
What drug class does Clevidipine belong to?
Clevidipine is in the Dihydropyridine Calcium Channel Blocker class.
What is the chemical formula of Clevidipine?
Clevidipine has the molecular formula C21H23Cl2NO6 and a molecular weight of 456.32 g/mol.
Browse: all drugs starting with C · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 674 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1237132 — compound record and bioactivity
- PubChem CID 153994 — chemical identifiers
- DrugBank DB04920 — drug record
- FDA UNII 19O2GP3B7Q — substance identity
- DailyMed: FDA labels for Clevidipine — current prescribing information (label search)
- UniProt Q13936 (CACNA1C) — target protein
- UniProt Q01668 (CACNA1D) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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