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GW-0742

GW-oh-74-2

Research profile · How we handle evidence

Category

Research Chemical

Compound type

Phase / Status

Research

Research chemical only

Standard Dose

10-20mg daily

As directed

Half-life

12-24 hours

Plasma elimination

Route(s)

OR / IN / TO

Oral, Injectable or Topical

Research Stage

Status Unknown

Research phase not specified; exercise appropriate caution.

Overview

GW-0742 is in the same research family as cardarine (GW-501516): both target the PPAR-delta pathway. The reason people talk about it is that PPAR-delta signaling is involved in how the body uses fuels, which is why the research focus often includes endurance and metabolic effects. The safety story is the hard part -- PPAR-delta agonists have shown cancer risk signals in preclinical studies, so this is not something to treat like a supplement.

Plain-language summary

GW-0742 is in the same research family as cardarine (GW-501516): both target the PPAR-delta pathway. The reason people talk about it is that PPAR-delta signaling is involved in how the body uses fuels, which is why the research focus often includes endurance and metabolic effects. The safety story is the hard part -- PPAR-delta agonists have shown cancer risk signals in preclinical studies, so this is not something to treat like a supplement.

Administration Routes

  • Oral
  • Injectable
  • Topical

Also known as

GW0742Cardarine 2.0GW-742Delta agonistPPAR-DNext-gen Cardarine

Mechanisms

1

PPAR-delta (PPAR-beta/delta) agonist

Detailed mechanism

GW-0742 is a highly selective PPAR-delta (peroxisome proliferator-activated receptor delta) agonist that binds to the nuclear receptor with greater selectivity for the delta subtype compared to GW-501516. Upon binding, it activates transcriptional programs governing fatty acid beta-oxidation in skeletal muscle and shifts cellular energy utilization toward fat oxidation, which in animal models correlates with improved endurance capacity. Like other PPAR-delta agonists, it has demonstrated concerning tumor-promoting activity in long-term rodent carcinogenicity studies, and it has not entered human clinical trials.

Safety

Side effects

  • Unknown in humans
  • Potential cancer risk

Reported benefits

  • Endurance enhancement
  • Metabolic benefits

Safety profile

Consult medical professional before use

Clinical trials

See research status

Structure

View 3D structure

Verified structure

GW-0742

Exact 2D structure can be rendered from a PubChem-backed canonical SMILES string.

Verified via PubChemMatched by casNumber
Source: PubChemLookup: 317318-84-6InChIKey HWVNEWGKWRGSRK-UHFFFAOYSA-N
Chemical Formula
C21H17F4NO3S2
Molecular Weight
471.5 g/mol
CAS Number
317318-84-6
InChIKey
HWVNEWGKWRGSRK-UHFFFAOYSA-N

Stack Context

No stack data available.

References

  1. 1

    A selective peroxisome proliferator-activated receptor delta agonist promotes reverse cholesterol transport (PNAS)

    2001

    View source
  2. 2

    Rationally designed PPARdelta-specific agonists and their therapeutic potential for metabolic syndrome: preclinical cancer signal discussion (PMC)

    2017

    View source
  3. 3

    Dangers of GW501516 (Cardarine) and related PPARdelta agonists including GW0742 - USADA advisory

    2018

    View source

This profile summarizes research literature for education only. It is not medical advice, and it does not diagnose, treat, or recommend a dose. Consult a qualified professional before changing a protocol.

Research-driven insights.Evidence-based decisions.