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Chemical Structure| 880635-03-0 Chemical Structure| 880635-03-0

Structure of GW6471
CAS No.: 880635-03-0

Chemical Structure| 880635-03-0

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GW6471 is a potent antagonist of PPARα.

4.5 *For Research Use Only !

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Product Details of GW6471

CAS No. :880635-03-0
Formula : C35H36F3N3O4
M.W : 619.67
SMILES Code : CCC(NC[C@@H](N/C(C)=C\C(C1=CC=C(C(F)(F)F)C=C1)=O)CC2=CC=C(OCCC3=C(C)OC(C4=CC=CC=C4)=N3)C=C2)=O
MDL No. :MFCD07784503
InChI Key :TYEFSRMOUXWTDN-DYQICHDWSA-N
Pubchem ID :446738

Safety of GW6471

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Isoform Comparison

Biological Activity

Target
  • PPARα

    PPARα, IC50:0.24 μM

In Vitro:

Cell Line
Concentration Treated Time Description References
mouse primary intestinal organoids 6 µM 24 hours GW6471 significantly decreased fatty acid uptake, indicating that GW6471 inhibited intestinal PPARα activation. PMC9970020
Hepa 1-6 cells 50 μM GW6471 abolished the upregulation of fatty acid oxidation gene expression downstream of PPARα induced by BMP9 treatment PMC7695473
Neonatal Rat Cardiomyocytes (NRCM) 10 μM 48 hours GW6471 partially abolished the anti-hypertrophic effects and metabolic effects of puerarin in NRCM. PMC7921143

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
mice high-fat diet (HFD) and high-fat, high-cholesterol, high-fructose diet (HFCFD)-induced obesity and nonalcoholic steatohepatitis (NASH) models oral 1 mg/kg Single dose, 60 minutes before BD induction GW6471 significantly reduced HFD-induced body weight gain, liver weight gain, hepatic steatosis, insulin resistance, and intestinal FABP1 expression levels, indicating that GW6471 improved obesity and NASH by inhibiting intestinal PPARα. PMC9970020
Mice HFpEF model Oral 1 week GW6471, a PPARα-specific antagonist, was used to reverse the protective effects of AdipoRon in HFpEF mice. PMC11785573
Rats Alzheimer's disease model Intraperitoneal injection 1 mg/kg body weight Daily for 4 weeks GW6471, as a PPAR-α antagonist, was co-administered with PEA to investigate the mechanism of PEA's action. The results showed that GW6471 completely abolished the PEA-induced control of Aβ1-42-induced increases in GFAP and S100B expression, indicating that PPAR-α plays a key role in the neuroprotective effects of PEA. PMC4540191

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.61mL

0.32mL

0.16mL

8.07mL

1.61mL

0.81mL

16.14mL

3.23mL

1.61mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

References

 

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