Tier B

Acetyl-L-Carnitine (ALC · ALCAR)

Also known as: ALC · ALCAR · Acetylcarnitine · Levocarnitine acetyl

1 PMID anchor · NEURO · METABOLISM · CELL · Last reviewed 2026-06-04

Mechanism of action

  • Carnitine ester form crossing the blood-brain barrier more efficiently than L-carnitine
  • Mitochondrial long-chain fatty acid β-oxidation substrate (acetyl-CoA donor)
  • Acetyl group donor for acetylcholine synthesis
  • Neurotrophic effect via nerve growth factor receptor modulation

Molecular + tissue targets

  • Mitochondrial fatty acid oxidation
  • Peripheral nerve regeneration markers
  • Cholinergic neurotransmission

Dosage range

1.5-3 g/day oral or IM-oral sequential dosing for peripheral neuropathic pain (Li 2015 PMID 25751285 PLoS One systematic review and meta-analysis of 4 RCT · n=523 · ALC vs control MD VAS 1.20 95% CI 0.68-1.72 P<0.00001 · stronger effect in diabetic subgroup); no severe adverse events reported across the trial pool

Safety notes

Common adverse events (pain, headache, paraesthesia, hyperaesthesia, GI symptoms) are mild and similar to control rates; thyroid disorder caution at very high doses; check for separately-marketed L-carnitine vs ALC formulation when comparing doses

Cross-market regulatory status

🇺🇸 FDA

GRAS · DSHEA dietary supplement · structure/function claims permitted; not an FDA-approved drug for any condition in the US

🇪🇺 EFSA

No standalone EFSA Reg 432/2012 authorized health claim adopted for acetyl-L-carnitine

🇧🇷 ANVISA

RDC 243/2018 dietary supplement · no IN 28/2018 Anexo V alegação funcional for acetil-L-carnitina

Common use cases

  • peripheral neuropathic pain (moderate effect at 1.5-3 g/day · stronger in diabetic patients)
  • mitochondrial bioenergetics adjunct in metabolic conditions
  • neurotrophic / cholinergic support framework
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