GW0742 Chemical Properties

Melting point:

134.5-135.5 °C

Boiling point:

591.5±60.0 °C(Predicted)

Density 

1.46±0.1 g/cm3(Predicted)

storage temp. 

2-8°C

solubility 

DMSO: >5 mg/mL

form 

solid

pka

3.17±0.10(Predicted)

color 

white

InChI

InChI=1S/C21H17F4NO3S2/c1-11-7-14(4-6-17(11)29-9-19(27)28)30-10-18-12(2)26-20(31-18)13-3-5-15(16(22)8-13)21(23,24)25/h3-8H,9-10H2,1-2H3,(H,27,28)

InChIKey

HWVNEWGKWRGSRK-UHFFFAOYSA-N

SMILES

C(O)(=O)COC1=CC=C(SCC2SC(C3=CC=C(C(F)(F)F)C(F)=C3)=NC=2C)C=C1C

Safety Information

WGK Germany 

3

HS Code 

38220090

MSDS

• Language:English Provider:SigmaAldrich

GW0742 Usage And Synthesis

Description

GW0742 is a PPARδ/β agonist very similar in molecular structure to GW501516 (Cardarine) — with the exception of one atom. It is often mentioned in comparison with Cardarine. This drug is mostly used by athletes to improve their stamina. The fat affecting properties of GW0742 also make it a good promoter of energy in the body. Additionally, this drug helps increase the oxidative abilities of your body muscles.

Chemical Properties

Light Yellow Solid

Uses

GW0742 is a small molecule agonist of the human Peroxisome Proliferator-Activated Recept δ (PPAR δ). It shows an EC50 of 1.1 nM against PPAR δ with 100-fold selectivity over the other human subtypes.

Definition

ChEBI: GW 0742 is a monocarboxylic acid.

Biological Activity

GW 0742 is a potent and highly selective PPARδ agonist. EC50 values are 0.001, 1.1 and 2 μM for transactivation of human PPARδ, -α, and -γ receptors respectively. Neuroprotective in rat cerebellar granule neuronal cultures after brief (12-hour) exposure but exhibits inherent toxicity after prolonged (48-hour) incubation. Increases rate of fatty acid oxidation and protects against ischemia/reperfusion injury in neonatal and adult cardiomyocytes.

storage

Desiccate at +4°C

GW0742(317318-84-6)Related Product Information

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• (2-METHYLPHENOXY)ACETIC ACID
• GW0742
• GW-501516