Documentation
Vendor-supplied data
COA stated as available
Not independently documented
Checked
Jul 18, 2026
Metabolic
Also known as: Acadesine Β· AICA riboside Β· 5-aminoimidazole-4-carboxamide ribonucleoside
An AMPK-activating small molecule (AICA ribonucleoside / acadesine), not a peptide, marketed as an 'exercise mimetic.' It went through large human cardiac-surgery trials that showed no benefit, is not approved anywhere, and is banned in sport by WADA.
Crystal Peptides. The table lists only product-specific offers that were checked and for which a real destination exists. Missing prices, quantities, stock and laboratory details are not inferred.
AICAR (5-aminoimidazole-4-carboxamide ribonucleoside), also called acadesine, is a small-molecule AMP analogue that activates AMP-activated protein kinase (AMPK). It is not a peptide. It is sold on the research-chemical market as an endurance / 'exercise-mimetic' and fat-loss agent, is unapproved for human use, and is on the WADA Prohibited List.
AICAR (as acadesine) has been studied in large human trials β but for cardioprotection during coronary artery bypass surgery, not fitness. The pivotal RED-CABG randomised trial (~3,000 patients) was stopped for futility and showed no benefit. No human evidence supports its marketed performance or fat-loss uses, and it has never been approved.
AICAR is unapproved for human use and prohibited in sport. In cardiac-surgery trials it was tolerated short-term under medical supervision, but higher-dose studies raised concerns such as kidney toxicity. Long-term safety outside a trial setting is not established.
A small-molecule AMPK activator, not a peptide. Not approved for human use in any jurisdiction (development as acadesine was discontinued). Prohibited at all times in sport by WADA as an S4 hormone and metabolic modulator.
Vendor comparison
The table lists only product-specific offers that were checked and for which a real destination exists. Missing prices, quantities, stock and laboratory details are not inferred.
Documentation
Vendor-supplied data
COA stated as available
Not independently documented
Checked
Jul 18, 2026
Affiliate disclosure: This page contains affiliate links. peptides.cx may receive a commission when a purchase is made through one of these links. Evidence ratings, safety summaries and editorial content are produced independently from vendor relationships.
AICAR (5-aminoimidazole-4-carboxamide ribonucleoside), also called acadesine, is a small-molecule AMP analogue that activates AMP-activated protein kinase (AMPK). It is not a peptide. It is sold on the research-chemical market as an endurance / 'exercise-mimetic' and fat-loss agent, is unapproved for human use, and is on the WADA Prohibited List.
AICAR (5-aminoimidazole-4-carboxamide ribonucleoside), also called acadesine or AICA riboside, is a small molecule, not a peptide, although it is sold on the same research-chemical market. It is an AMP analogue: inside cells it is converted to ZMP, which mimics AMP and activates AMP-activated protein kinase (AMPK), a cellular energy sensor. AMPK activation is reported to increase fatty-acid oxidation, glucose uptake, and mitochondrial biogenesis, which is where the exercise-mimetic marketing comes from. It is not approved for human use in any jurisdiction, development as acadesine was discontinued, and it is prohibited at all times in sport by WADA as an S4 hormone and metabolic modulator.
peptides.cx grades the evidence B, which is easy to misread: it reflects the existence of large, well-conducted human trials, not evidence that AICAR does what it is marketed to do. AICAR, as acadesine, was studied in large human trials of cardioprotection during coronary artery bypass surgery, not in athletes and not for body composition. The pivotal RED-CABG randomised trial, with roughly 3,000 patients, was stopped for futility and showed no benefit. The endurance story comes from rodent work reporting increased endurance and metabolic changes, which never translated into demonstrated human benefit. A systematic review also cautions that many AICAR effects are AMPK-independent, so its pharmacology is less clean than usually presented.
AICAR is unapproved for human use and banned in sport, and both facts matter practically. In the cardiac-surgery trials it was tolerated short-term under medical supervision, but kidney toxicity was reported in clinical studies at the higher exposures tested, and long-term safety outside a trial setting is not established. Anti-doping authorities also note potential risks from excessive or inappropriate AMPK activation. For any tested athlete it is prohibited in and out of competition, and its full adverse-effect profile for non-medical use is not established. This page is an educational reference summarising what the science does and does not show; it is not medical advice, and it does not provide dosing, protocols, or sourcing guidance.
Evidence grade: B
AICAR (as acadesine) has been studied in large human trials β but for cardioprotection during coronary artery bypass surgery, not fitness. The pivotal RED-CABG randomised trial (~3,000 patients) was stopped for futility and showed no benefit. No human evidence supports its marketed performance or fat-loss uses, and it has never been approved. Rodent studies popularised AICAR as an 'exercise mimetic,' reporting increased endurance and metabolic changes. These animal findings drove interest but did not translate into demonstrated human benefit.
AICAR (as acadesine) has been studied in large human trials β but for cardioprotection during coronary artery bypass surgery, not fitness. The pivotal RED-CABG randomised trial (~3,000 patients) was stopped for futility and showed no benefit. No human evidence supports its marketed performance or fat-loss uses, and it has never been approved.
Rodent studies popularised AICAR as an 'exercise mimetic,' reporting increased endurance and metabolic changes. These animal findings drove interest but did not translate into demonstrated human benefit.
AICAR is unapproved for human use and prohibited in sport. In cardiac-surgery trials it was tolerated short-term under medical supervision, but higher-dose studies raised concerns such as kidney toxicity. Long-term safety outside a trial setting is not established.
A small-molecule AMPK activator, not a peptide. Not approved for human use in any jurisdiction (development as acadesine was discontinued). Prohibited at all times in sport by WADA as an S4 hormone and metabolic modulator.