• GW0742

GW0742

  • CasNo:317318-84-6
  • Purity:99%

Product Details;

CasNo: 317318-84-6

Molecular Formula: C21H17 F4 N O3 S2

Appearance: White to off-white solid

High Purity Wholesale Price GW0742 317318-84-6 good producer

  • Molecular Formula:C21H17 F4 N O3 S2
  • Molecular Weight:471.496
  • Appearance/Colour:White to off-white solid 
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:134.5-135.5 °C 
  • Boiling Point:591.476oC at 760 mmHg 
  • PKA:3.17±0.10(Predicted) 
  • Flash Point:311.514oC 
  • PSA:112.96000 
  • Density:1.462g/cm3 
  • LogP:6.34050 

GW0742(Cas 317318-84-6) Usage

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.

Biological Activity

Potent and highly selective PPAR δ agonist. EC 50 values are 0.001, 1.1 and 2 μ M for transactivation of human PPAR δ , - 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.

InChI:InChI=1/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)

317318-84-6 Relevant articles

Parallel Chemistry Approach to Identify Novel Nuclear Receptor Ligands Based on the GW0742 Scaffold

Teske, Kelly A.,Rai, Ganesha,Nandhikonda, Premchendar,Sidhu, Preetpal S.,Feleke, Belaynesh,Simeonov, Anton,Yasgar, Adam,Jadhav, Ajit,Maloney, David J.,Arnold, Leggy A.

, p. 646 - 656 (2017/10/13)

We describe the parallel synthesis of no...

Medicaments

-

, (2008/06/13)

Methods or prevention or treatment of di...

Novel selective small molecule agonists for peroxisome proliferator-activated receptor δ (PPARδ) - Synthesis and biological activity

Sznaidman, Marcos L.,Haffner, Curt D.,Maloney, Patrick R.,Fivush, Adam,Chao, Esther,Goreham, Donna,Sierra, Michael L.,LeGrumelec, Christelle,Xu, H. Eric,Montana, Valerie G.,Lambert, Millard H.,Willson, Timothy M.,Oliver Jr., William R.,Sternbach, Daniel D.

, p. 1517 - 1521 (2007/10/03)

We report the synthesis and biological a...

Activator of PPAR delta

-

, (2008/06/13)

Compounds of Formula (I) are disclosed. ...

317318-84-6 Process route

C<sub>25</sub>H<sub>25</sub>F<sub>4</sub>NO<sub>3</sub>S<sub>2</sub>

C25H25F4NO3S2

GW 0742
317318-84-6

GW 0742

Conditions
Conditions Yield
With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 1h;
tert-butyl 2-(4-(((2-bromo-4-methylthiazol-5-yl)methyl)thio)-2-methylphenoxy)acetate

tert-butyl 2-(4-(((2-bromo-4-methylthiazol-5-yl)methyl)thio)-2-methylphenoxy)acetate

GW 0742
317318-84-6

GW 0742

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: sodium carbonate / 1,2-dimethoxyethane / 0.5 h / 150 °C / Inert atmosphere; Sealed tube; Microwave irradiation
2: trifluoroacetic acid / dichloromethane / 1 h / 20 °C
With sodium carbonate; trifluoroacetic acid; In 1,2-dimethoxyethane; dichloromethane; 1: |Suzuki Coupling;

317318-84-6 Upstream products

  • 876-02-8
    876-02-8

    4-hydroxy-3-methylphenyl methyl ketone

  • 56077-47-5
    56077-47-5

    (4-mercapto-2-methyl-phenoxy)-acetic acid methyl ester

  • 317319-10-1
    317319-10-1

    methyl (4-hydroxy-2-methylphenoxy)acetate

  • 166953-80-6
    166953-80-6

    (4-acetyl-2-methylphenoxy)acetic acid methyl ester

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