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SIDE-BY-SIDE EVIDENCE

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Select 2–3 profiles from the English Library. Class and grade describe evidence and regulatory context, not comparative effectiveness or suitability for an individual.

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SIDE-BY-SIDE EVIDENCE VIEW

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Evidence comparison · not a treatment ranking
Evidence boundaries, not cross-trial treatment outcomes
Molecule
Cardarine / GW501516: Conceptual scientific illustrationCardarine / GW501516
SR9009: Conceptual scientific illustrationSR9009
AICAR (Acadesine): Conceptual scientific illustrationAICAR (Acadesine)
Research TopicClinical / Endocrine PharmacologyMitochondrial / Metabolic ResearchMitochondrial / Metabolic Research
PharmacologyExperimental PPAR-beta/delta agonist; not a SARMExperimental small molecule / REV-ERB-related researchInvestigational purine nucleoside analogue / adenosine-regulating agent; not a peptide
PrimeCore ClassClass BInvestigationalClass CExperimental / limited evidenceClass BInvestigational
Evidence GradeGrade BStrong controlled human evidenceGrade EPreclinical evidenceGrade BStrong controlled human evidence
Evidence boundaryCardarine, GW501516 and GW1516 identify an experimental PPAR-beta/delta agonist, not a SARM or anabolic steroid. Short controlled human studies reported lipid-biomarker changes but did not establish cardiovascular-event reduction, fat loss, endurance benefit or long-term safety. Animal studies report tumour-promoting signals in susceptible models; these do not quantify human incidence but preclude a proven-safety claim. WADA 2026 prohibits GW501516 at all times as a metabolic modulator.SR9009 is an experimental small molecule, not a SARM or peptide. Genetic studies demonstrate REV-ERB-independent effects, limiting target-specific claims. Cell and mouse results do not establish human fat-loss, endurance or cardiac benefit, and human safety remains unverified.A nucleoside analogue and AMPK-related research compound, not a peptide; clinical and anti-doping contexts must be separated.
Unknowns

Insufficient data in the current dataset

Insufficient data in the current dataset

  • long-term safety outside short perioperative research settings
  • human risk-benefit for weight, metabolic or performance claims
  • effects of repeated exposure on purine, glucose and lipid metabolism
  • comparability of research-grade AICAR, acadesine formulations and online products
  • current product-specific marketing-authorisation status in Thailand, the EU and UK
  • current US compounding-list status under a substance-specific FDA review
Limitations
  • PPAR-delta agonist ≠ SARM; lipid biomarker change ≠ cardiovascular benefit; mouse tumour signal ≠ quantified human incidence but cannot be dismissed as proof of safety

English translation is not yet verified for 1 excerpt(s). This is a language gap, not an absence of risks or uncertainty.

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  • SR9009 ≠ SARM; mouse metabolism ≠ human exercise benefit; เป้าหมายที่คาดไม่เท่ากับกลไกที่พิสูจน์ครบ
  • Strong controlled human evidence exists only in a narrow CABG setting and culminated in a negative confirmatory trial. Older meta-analytic and post-hoc signals must be interpreted in light of RED-CABG. Popular performance claims are based mainly on mouse work. Mechanistic studies also show that AICAR is not selective for AMPK, limiting simple pathway-based conclusions.
Sources
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Complete evidence profile (Thai)

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Complete evidence profile (Thai)

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Complete evidence profile (Thai)

This table does not compare doses, cross-trial outcomes or individual suitability. Missing information does not establish an absence of risk.

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Missing fields mean information is unavailable in the current structured dataset, not that a molecule has no risks or uncertainties. English translations retain the original evidence boundaries. Where translation is not yet verified, the original Thai excerpts remain available under an explicit label. Sources retain their original language.

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