Levocarnitine
Carnitine Analog — ALIMENTARY TRACT AND METABOLISM
Also known as: (-)-Carnitine, (-)-L-Carnitine, (R)-Carnitine, carniking, carnilean, carnitene, carnitine, carnivit, l-Carnitine, levocarnitine HCl, levocarnitine hydrochloride
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Levocarnitine is an ofp drug in the Carnitine Analog class catalogued in DrugCentral. It was first approved by the FDA in 1985. DrugCentral lists 3 molecular targets, including Cpt1b, Cpt2 and CPT1A. Recorded indications include Carnitine deficiency.
- Approval status: ofp (first approved 1985 by the FDA).
- Drug class: Carnitine Analog.
- Molecular targets: Cpt1b, Cpt2 and CPT1A (3 listed in DrugCentral).
- Indications: Carnitine deficiency.
- ATC code: A16AA01 (Amino acids and derivatives).
- Molecular formula: C7H15NO3; molecular weight 161.20 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Carnitine deficiency
Off-label uses (1)
- Recovery during viral myocarditis
Contraindications (7)
- Blood coagulation disorder
- Disease of liver
- Kidney disease
- Low blood pressure
- Obstruction of bile duct
- Seizure disorder
- Vitamin K Deficiency Induced Hypoprothrombinemia
Mechanism & targets
| Established pharmacologic class | Carnitine Analog |
|---|
Molecular targets (3)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Carnitine O-palmitoyltransferase 1, muscle isoform | Cpt1b | unknown | Ki 4.00 |
| Carnitine palmitoyltransferase 2 | Cpt2 | unknown | Ki 4.00 |
| Carnitine O-palmitoyltransferase 1, liver isoform | CPT1A | unknown | — |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 1985-12-27 | FDA | — | SIGMA TAU | Yes |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
A16AA01 | ALIMENTARY TRACT AND METABOLISM › OTHER ALIMENTARY TRACT AND METABOLISM PRODUCTS › OTHER ALIMENTARY TRACT AND METABOLISM PRODUCTS › Amino acids and 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 |
|---|---|
| Seizure | 329.4 |
| Parenteral nutrition associated liver disease | 188.8 |
| Hyperammonaemia | 155.8 |
| Status epilepticus | 112.2 |
| Fanconi syndrome | 79.9 |
| Ammonia increased | 73.1 |
| Epilepsy | 68.6 |
| Upper respiratory tract inflammation | 58.8 |
| Hypophosphataemic osteomalacia | 45.2 |
| Metabolic acidosis | 43.6 |
| Somnolence | 42.9 |
| Seizure cluster | 41.4 |
Chemical structure
Full physicochemical, ADMET and 3D-structure analysis of Levocarnitine is on its molecule page.
| Molecular formula | C7H15NO3 |
|---|---|
| Molecular weight | 161.20 g/mol |
| CAS number | — |
| InChIKey | PHIQHXFUZVPYII-ZCFIWIBFSA-N |
| PubChem CID | 10917 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Levocarnitine used for?
DrugCentral lists the following indications for Levocarnitine: Carnitine deficiency.
How does Levocarnitine work?
Its molecular targets in DrugCentral include Cpt1b, Cpt2 and CPT1A.
When was Levocarnitine first approved?
Levocarnitine was first approved by the FDA in 1985.
What drug class does Levocarnitine belong to?
Levocarnitine is in the Carnitine Analog class.
What is the chemical formula of Levocarnitine?
Levocarnitine has the molecular formula C7H15NO3 and a molecular weight of 161.20 g/mol.
Browse: all drugs starting with L · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 513 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1149 — compound record and bioactivity
- PubChem CID 10917 — chemical identifiers
- DrugBank DB00583 — drug record
- FDA UNII 0G389FZZ9M — substance identity
- DailyMed: FDA labels for Levocarnitine — current prescribing information (label search)
- UniProt P50416 (CPT1A) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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