For laboratory and research use only. Not for human consumption.

AICAR Alternatives

Explore peptides similar to AICAR. Compare mechanisms, effects, and find the best alternative for your research.

Original

AICAR

Metabolic

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AICAR is not a peptide at all. It is a small nucleoside (a building block related to the purine pathway) that cells convert into ZMP, a molecule that mimics AMP and switches on AMPK, the cell's energy sensor. It became famous in 2008 when a Salk Institute study showed sedentary mice on AICAR ran 44% further, earning it the "exercise in a pill" label. Human data tell a much less exciting story: it was tested as an intravenous drug (acadesine) for heart surgery and leukemia, the big heart trial failed, and nothing is approved.

Similar Peptides

Pancragen

Metabolic

Pancragen is a synthetic tetrapeptide bioregulator, Lys-Glu-Asp-Trp (KEDW), from the Khavinson group, designed to target pancreatic tissue. It is studied for supporting blood-sugar control and the insulin-producing endocrine pancreas, especially in aging. It is a research compound with no approval and no published human clinical trials. The notable evidence comes from aged primates, not people.

THR-123

Metabolic

THR-123 is a small synthetic 16-residue cyclic peptide designed to mimic part of the protein BMP7 (bone morphogenetic protein 7) and switch on its receptor, ALK3, in the kidney. It was developed by Thrasos Therapeutics and made famous by a 2012 Nature Medicine paper showing that, taken orally, it could reverse kidney fibrosis and trigger kidney regeneration in mice. It is a preclinical research compound with no human trials of its own, though its intravenous sibling THR-184 reached Phase 2 for acute kidney injury.

SLU-PP-332

Metabolic

SLU-PP-332 is a small synthetic molecule, not a peptide, that turns on the estrogen-related receptors (ERRalpha, beta and gamma), the master switches behind much of the body's response to endurance exercise. Researchers call it an 'exercise mimetic' because in mice it boosts mitochondria, shifts muscle toward fatigue-resistant fibers, improves stamina and trims fat without the animal moving more. It was made as a lab tool to study exercise biology. There are no human trials.

Retatrutide

Weight Loss

Retatrutide is the heavy hitter of the new weight-loss drugs: a once-weekly injectable peptide that hits three receptors at once - GIP, GLP-1, and glucagon - earning it the nickname triple-G agonist. In phase 2 it produced about 24 percent weight loss at the top dose, and in the phase 3 TRIUMPH-1 trial Lilly reported 28.3 percent at 12 mg over 80 weeks. It is investigational, made by Eli Lilly, and not FDA approved; Lilly plans to file with the FDA in the first quarter of 2027. Because it is not an approved drug, FDA says it cannot be legally compounded.

MK-677

Growth Hormone

MK-677 (ibutamoren) is not actually a peptide, it is a small, orally active non-peptide molecule that mimics ghrelin, your hunger and growth-hormone hormone. Taken as a daily pill, it reliably pushes up growth hormone and IGF-1 levels, which is why it is popular for muscle and recovery. It has been through real human trials but was never approved as a drug, and the trials that mattered most for older adults and Alzheimer's came up short.

Orforglipron

Weight Loss

FDA

Orforglipron is Eli Lilly's oral, once-daily GLP-1 receptor agonist, and the headline is that it is a small molecule, not a peptide, so it survives the gut and can be taken as a plain pill with no food or water restrictions. It is being developed for type 2 diabetes and obesity and has completed multiple successful Phase 3 trials. As of mid-2026 it is filed for regulatory review but not yet approved.

All Metabolic Peptides

Pancragen

Pancragen is a synthetic tetrapeptide bioregulator, Lys-Glu-Asp-Trp (KEDW), from the Khavinson group, designed to target pancreatic tissue. It is studied for supporting blood-sugar control and the insulin-producing endocrine pancreas, especially in aging. It is a research compound with no approval and no published human clinical trials. The notable evidence comes from aged primates, not people.

SLU-PP-332

SLU-PP-332 is a small synthetic molecule, not a peptide, that turns on the estrogen-related receptors (ERRalpha, beta and gamma), the master switches behind much of the body's response to endurance exercise. Researchers call it an 'exercise mimetic' because in mice it boosts mitochondria, shifts muscle toward fatigue-resistant fibers, improves stamina and trims fat without the animal moving more. It was made as a lab tool to study exercise biology. There are no human trials.

THR-123

THR-123 is a small synthetic 16-residue cyclic peptide designed to mimic part of the protein BMP7 (bone morphogenetic protein 7) and switch on its receptor, ALK3, in the kidney. It was developed by Thrasos Therapeutics and made famous by a 2012 Nature Medicine paper showing that, taken orally, it could reverse kidney fibrosis and trigger kidney regeneration in mice. It is a preclinical research compound with no human trials of its own, though its intravenous sibling THR-184 reached Phase 2 for acute kidney injury.

Quick Comparison

PeptideCategoryFDA StatusAction
AICARMetabolicNot ApprovedOriginal
PancragenMetabolicNot ApprovedCompare →
THR-123MetabolicNot ApprovedCompare →
SLU-PP-332MetabolicNot ApprovedCompare →
RetatrutideWeight LossNot ApprovedCompare →