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MONOGRAPH No. 068
TYPE
Nucleotide analogue / not a peptide
MW
258.23 g/mol
CAS
2627-69-2
EU STATUS
Research only
WADA
Prohibited S4 (AMPK activators)
MIN PURITY
≥98% HPLC
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AICAR — EU research guide.

AICAR (5-aminoimidazole-4-carboxamide ribonucleotide) is a cell-permeable AMP-mimetic that directly activates AMPK, the master metabolic switch. It is widely used in metabolic research and is prohibited by WADA.

Last reviewed:

What is AICAR?

AICAR is converted intracellularly to ZMP, an AMP mimetic that activates AMPK by simulating energy depletion. AMPK activation switches cells from anabolic to catabolic metabolism: increasing fatty acid oxidation, glucose uptake, mitochondrial biogenesis and reducing mTOR signalling. Note: AICAR is not a peptide but a nucleotide derivative; it appears in peptide research databases due to its common co-use in metabolic research.

What does the research show?

Seminal mouse studies (Evans lab, Salk Institute) showed ~44% improvement in running endurance with AICAR alone, without exercise. Extensive use in diabetes, obesity and mitochondrial disease research. AICAR activates PGC-1α and increases GLUT4 expression. The exercise-mimicking profile attracted significant sports doping research interest. No approved human therapeutic as of mid-2026.

EU legal status

Not approved as a medicine in the EU. WADA-prohibited in sport (S4 — Hormone and metabolic modulators). Available for laboratory metabolic research only.

WADA-prohibited. Not a peptide — nucleotide derivative. No human therapeutic approval. Not for human use or use in competitive athletes. This is a research compound, not a medication.
✓ PeptideCompare lists AICAR from EU research vendors. WADA prohibition status should be clearly noted on any research documentation.

Molecular information

Molecular formula
C9H14N4O5
Molecular weight
258.23 g/mol
CAS number
2627-69-2
Source: PubChem CID 17513

Pharmacokinetics

No established human pharmacokinetic data. Published human PK parameters for this compound are not available; reported data are limited to animal models or absent. No curve is shown, to avoid implying data that does not exist.

Potency retained over time

Each line is one storage condition: it starts at 100% and falls as potency is lost. Above the dashed 80% line the material is considered reliable — hover for exact values.

Freezer −20 °C
36+ mo
Stable · >95% potency
Fridge 4 °C
3-5 mo
In use · after recon
Room 20 °C
3-4 wks
Limited · moderate loss
Warm 37 °C+
2-3 days
Poor · accelerated loss

⚠ A structural estimate, derived from each compound's sequence length, cyclisation and oxidation-, deamidation- and light-sensitive residues. Indicative only — not lab-measured per batch.

AICAR across EU suppliers

COA-verified EU vendors · Updated monthly

References

  1. The paper behind the 'exercise in a pill' phrase: in sedentary mice, 4 weeks of oral AICAR alone induced metabolic genes and increased treadmill running endurance by 44%, working through the AMPK-PPARδ pathway. This is a mouse result, not a demonstrated human endurance benefit. Narkar VA, Downes M, Yu RT, et al. Cell. 2008;134(3):405–415. DOIPubMed 18674809PMC
  2. The mechanism source: AICA riboside (AICAR) increases AMP-activated protein kinase activity, fatty-acid oxidation and glucose uptake in rat muscle. This defines what AICAR does at the cellular level and predates the endurance framing by a decade. Merrill GF, Kurth EJ, Hardie DG, Winder WW. Am J Physiol. 1997;273(6 Pt 1):E1107–E1112. PubMed 9435525

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