This page describes pharmacological agents that may have legal restrictions, side effects, and drug interactions in your jurisdiction. Information is for educational research only — consult a clinician before considering any compound.

High-risk compound

Surface here is educational only; do not use without medical supervision. Our editorial verdict is SKIP-FOR-NOW — current cost / risk / redundancy puts it below the line.

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Cardarine

Investigational Drug — Program Terminated

See GW-501516 — Cardarine is the most common gym/forum/vendor name for the PPARδ agonist GW-501516. NOT a SARM. Abandoned by GSK in 2007 after rat multi-organ carcinogenicity. WADA S4.5 banned.

Aliases (8)
GW-501516 · GW1516 · GW501516 · GW 501 · 516 · Endurobol · the exercise-mimetic · CARDARINE
TYPICAL DOSE
10-20 mg/day (community); see GW-501516 for ful…
See GW-501516
ROUTE
Oral
Oral
CYCLE
8-12 weeks (community); not recommended
Refer to canonical entry
STORAGE
Room temp; cool dry place
Room temp; cool dry place

Overview

What is Cardarine?

Cardarine is the most common gym, forum, MMA, endurance-cycling, and research-chem-vendor name for GW-501516 — a high-affinity selective PPARδ agonist originally developed by GlaxoSmithKline and Ligand Pharmaceuticals (early 2000s) for dyslipidemia and metabolic syndrome. The two names refer to the same molecule. NOT a SARM (does not bind the androgen receptor). Abandoned by GSK in 2007 after rat multi-organ carcinogenicity findings. WADA Prohibited List S4.5 (Metabolic Modulators — PPARδ agonists named, banned in- and out-of-competition). FDA-prohibited in dietary supplements. Sold gray-market as research chemical only. See the canonical entry at GW-501516 for full mechanism, evidence, dosing, side effects, sourcing, decision matrix, biomarkers, controversies, and verdict rationale.

Key Benefits

See GW-501516 entry. Summary: PPARδ activation → fatty acid oxidation upregulation → mitochondrial biogenesis → endurance + fat loss; favorable Phase 2 lipid effects (HDL ↑, triglycerides ↓, ApoB ↓, insulin sensitivity ↑) at 2.5-10 mg/day for 12 weeks. Real metabolic exercise-mimetic effect on the muscle/cardiac mitochondrial-biogenesis subset of training adaptation. Does NOT reproduce cardiovascular, neural, hormonal, or bone-loading adaptations of actual training.

Mechanism of Action

Same as GW-501516. Selective high-affinity agonist of PPARδ; ~1000-fold selectivity over PPARα and PPARγ. Activates the β-oxidation gene set, upregulates PGC-1α, drives Type I/IIa oxidative muscle fiber program. NOT a SARM. Hepatically metabolized; ~24h half-life. See canonical entry.

Pharmacokinetics

·
PeakHalf-life
Approximate curve — visual aid only, not data-precise PK

Quality Indicators

!

Sold as 'SARM' by many vendors — pharmacologically wrong

Many research-chem vendors mislabel Cardarine as a SARM. It is NOT a SARM. Verify product label says GW-501516 / Cardarine; confirm via COA. The mislabeling leads users to assume SARM PCT and bloodwork frameworks apply — they do not. See GW-501516 for full sourcing guidance.

What to Expect

  • Week 1
    Tolerability and dose-response.
  • Week 2-4
    Early effect window.
  • Week 4-8
    Peak benefit assessment.
  • Week 8+
    Cycle decision point.
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