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ChemicalBook > Product Catalogue >Biochemical Engineering >Inhibitors >Metabolism >PPAR agonists >GW0742

GW0742

GW0742 Structure
  • ₹20556.68 - ₹71141.9
  • Product name: GW0742
  • CAS: 317318-84-6
  • MF: C21H17F4NO3S2
  • MW: 471.49
  • EINECS:1532714-185-1
  • MDL Number:MFCD07369423
  • Synonyms:2-(4-(((2-(3-Fluoro-4-(trifluoromethyl)phenyl)-4-methylthiazol-5-yl)methyl)thio)-2-methylphenoxy);GW 0742X;GW 610742;GWdelta 0742;2-(4-(((2-(3-Fluoro-4-(trifluoromethyl)phenyl)-4-methylthiazol-5-yl)methyl)thio)-2-methylpheno;GW0742;[4-[[[2-[3-FLUORO-4-(TRIFLUOROMETHYL)PHENYL]-4-METHYL-5-THIAZOLYL]METHYL]THIO]-2-METHYLPHENOXY]ACETIC ACID;4-[2-(3-FLUORO-4-TRIFLUOROMETHYL-PHENYL)-4-METHYL-THIAZOL-5-YLMETHYLSULFANYL]-2-METHYL-PHENOXY-ACETIC ACID
2 prices
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Brand

  • Sigma-Aldrich(India)

Package

  • 1MG
  • 5MG
  • ManufacturerSigma-Aldrich(India)
  • Product numberG3295
  • Product descriptionGW0742 ≥98% (HPLC)
  • Packaging1MG
  • Price₹20556.68
  • Updated2022-06-14
  • Buy
  • ManufacturerSigma-Aldrich(India)
  • Product numberG3295
  • Product descriptionGW0742 ≥98% (HPLC)
  • Packaging5MG
  • Price₹71141.9
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) G3295 GW0742 ≥98% (HPLC) 1MG ₹20556.68 2022-06-14 Buy
Sigma-Aldrich(India) G3295 GW0742 ≥98% (HPLC) 5MG ₹71141.9 2022-06-14 Buy

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

Symbol(GHS):
Signal word:
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
Precautionary statements:

Description

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.

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