Metabolic research
AICAR
Lyophilized metabolic research compound
AICAR is an AMPK-pathway research compound used as a reference in cellular energy-sensing, glucose uptake, lipid metabolism, and exercise-mimetic literature.
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Contexte de recherche
Profil de recherche AICAR
AICAR is an adenosine analog used as a laboratory reference in cellular energy-sensing research. Inside cells it can be converted to ZMP, an AMP-like metabolite associated with activation of AMP-activated protein kinase and other AMP-sensitive processes. Researchers use AICAR in cell and animal models to examine glucose transport, fatty-acid oxidation, mitochondrial signaling, gene expression, and exercise-mimetic hypotheses. It is not a peptide, and its experimental behavior depends strongly on cell type, concentration, exposure time, and metabolic context. AICAR is generally selected when a study requires a direct AMPK-adjacent tool compound rather than an incretin or receptor-agonist peptide.
Molecular class
Small-molecule AMP mimetic
Sequence / composition
5-Aminoimidazole-4-carboxamide ribonucleotide; a purine-nucleoside analog rather than an amino-acid peptide.
Research design note
Intracellular phosphorylation to ZMP is central to its use as an energy-sensing pathway tool compound.
Mécanisme proposé
An adenosine analog taken up by cells and phosphorylated to ZMP, an AMP mimetic. ZMP can activate AMPK and influence other AMP-sensitive enzymes, shifting signaling toward energy conservation, glucose uptake, fatty-acid oxidation, and mitochondrial adaptation.
Effets rapportés dans les études
- Cell studies report AMPK phosphorylation, increased glucose transport, altered lipid metabolism, and changes in mitochondrial and metabolic gene expression.
- Animal studies reported increased oxidative capacity and endurance-like effects in selected skeletal-muscle models.
- AICAR is not perfectly AMPK specific; ZMP affects additional nucleotide-sensitive pathways and can produce model-dependent effects.
Critères de recherche courants
AMPK phosphorylation, ACC phosphorylation, glucose uptake, fatty-acid oxidation, mitochondrial gene expression, oxygen consumption, muscle-fiber markers, and endurance performance.
Preuves et limites
The strongest evidence is mechanistic and preclinical. AICAR is a pathway tool compound, not a selective peptide receptor ligand.
External reading
Literature for context—not product proof.
Third-party sources describe their own research materials and methods. They do not validate a specific Azure catalog batch.
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