GW7647
- Product Name
- GW7647
- CAS No.
- 265129-71-3
- Chemical Name
- GW7647
- Synonyms
- GW647;CS-761;GW7647;GW 7647X;GWalpha 7647;GW7647, >=98%;GW7647; GW 7647;GW7647, 10 mM in DMSO;GW7647, PPARalpha agonist;GW7647 - CAS 265129-71-3 - Calbiochem
- CBNumber
- CB5420133
- Molecular Formula
- C29H46N2O3S
- Formula Weight
- 502.75
- MOL File
- 265129-71-3.mol
GW7647 Property
- Melting point:
- 156 - 157°C
- Boiling point:
- 693.9±55.0 °C(Predicted)
- Density
- 1.12
- storage temp.
- Store at RT
- solubility
- DMSO: 16 mg/mL, soluble
- form
- White solid
- pka
- 3.79±0.10(Predicted)
- color
- white
- InChIKey
- PKNYXWMTHFMHKD-UHFFFAOYSA-N
- SMILES
- C(O)(=O)C(SC1=CC=C(CCN(C(NC2CCCCC2)=O)CCCCC2CCCCC2)C=C1)(C)C
Safety
- WGK Germany
- 3
N-Bromosuccinimide Price
- Product number
- G6793
- Product name
- GW7647
- Purity
- ≥98% (HPLC)
- Packaging
- 5mg
- Price
- $249
- Updated
- 2025/07/31
- Product number
- 370698
- Product name
- GW7647
- Packaging
- 5mg
- Price
- $389
- Updated
- 2025/07/31
- Product number
- 10008613
- Product name
- GW 7647
- Purity
- ≥98%
- Packaging
- 1mg
- Price
- $37
- Updated
- 2024/03/01
- Product number
- 10008613
- Product name
- GW 7647
- Purity
- ≥98%
- Packaging
- 5mg
- Price
- $142
- Updated
- 2024/03/01
- Product number
- G6793
- Product name
- GW7647
- Purity
- ≥98% (HPLC)
- Packaging
- 25mg
- Price
- $980
- Updated
- 2025/07/31
GW7647 Chemical Properties,Usage,Production
Description
Peroxisome proliferator-
Uses
GW7647 has been used as a peroxisome proliferator-activated receptor α (PPAR α) ligand:
- in defatting medium to treat primary human hepatocytes
- to test its effect on the glycolytic function in cardiomyocytes
- to test its effect on infant mouse heart
- in breast cancer MDA-MB-231 cells to activate PPARs
Uses
GW 7647 is a potent PPARα agonist with 200-fold selectivity over PPARγ and PPARδ. It can also be used for regenerative cardiac cell therapies.
Definition
ChEBI: A monocarboxylic acid that is 2-(phenylsulfanyl)isobutyric acid in which the phenyl group is substituted at the para- position by a 3-aza-7-cyclohexylhept-1-yl group in which the nitrogen is acylated by a (cyclohexylamino)carbonyl group.
General Description
A cell-permeable urea-substituted thioisobutyric acid (ureido-TiBA) compound that acts as a potent and selective PPARα agonist (PPARα, γ and δ - EC50 = 6 nM, 1.1 μM and 6.2 μM for human; 1 nM, 1.3 μM and 2.9 μM for murine, respectively). Also displays in vivo lipid-lowering activity in rats.
Biological Activity
Potent and highly selective PPAR α agonist (EC 50 values are 6, 1100 and 6200 nM for human PPAR α , PPAR γ and PPAR δ receptors respectively). Modulates oleate metabolism and mitochondrial enzyme gene expression in mature myotubules in vitro . Has lipid-lowering effects following oral administration in vivo .
Biochem/physiol Actions
GW7647 reduces serum triglyceride levels and enhances hepatic expression of genes associated with β-oxidation. Usage of GW7647 along with metformin in conditions of liver steatosis or injury improves the enzymatic levels of aspartate transaminase (AST) and alanine transaminase (ALT) in serum.
storage
Store at RT
References
[1] PETER J. BROWN. Identification of a subtype selective human PPARα agonist through parallel-array synthesis[J]. Bioorganic & Medicinal Chemistry Letters, 2001, 11 9: Pages 1225-1227. DOI: 10.1016/s0960-894x(01)00188-3
[2] LISA BAUMGARTNER. Lignan Derivatives from Krameria lappacea Roots Inhibit Acute Inflammation in Vivo and Pro-inflammatory Mediators in Vitro[J]. Journal of Natural Products , 2011, 74 8: 1779-1786. DOI: 10.1021/np200343t
[3] STEPAN ALESHIN. Peroxisome proliferator-activated receptor (PPAR)-gamma positively controls and PPARalpha negatively controls cyclooxygenase-2 expression in rat brain astrocytes through a convergence on PPARbeta/delta via mutual control of PPAR expression levels.[J]. Molecular Pharmacology, 2009, 76 2: 414-424. DOI: 10.1124/mol.109.056010
GW7647 Preparation Products And Raw materials
Raw materials
Preparation Products
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