GW 9662
Tocris Bioscience | Catalog # 1508
Key Product Details
Description
Product Description
GW 9662 is a selective irreversible PPARγ antagonist (IC50 values are 3.3, 32 and 2000 nM for PPARγ, PPARα and PPARδ respectively). Blocks the inhibition of osteoclast formation induced by IL-4 in the low micromolar range (1-2 μM), therefore is more potent than BADGE. Anticancer, inhibits growth of human mammary tumor cell lines.
Product Specifications for GW 9662
Molecular Weight
Formula
Storage
Purity
Chemical Name
CAS Number
PubChem ID
InChI Key
SMILES
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 27.67 | 100 | |
| Ethanol | 6.92 | 25 with gentle warming |
Preparing Stock Solutions for GW 9662
The following data is based on the product molecular weight 276.68.
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 3.61 mL | 18.07 mL | 36.14 mL |
| 5 mM | 0.72 mL | 3.61 mL | 7.23 mL |
| 10 mM | 0.36 mL | 1.81 mL | 3.61 mL |
| 50 mM | 0.07 mL | 0.36 mL | 0.72 mL |
Calculators
Background References
References are publications that support the biological activity of the product. See our Citations tab to view 110 publications citing the usage of this product.
- Leesnitzer Functional consequences of cysteine modification in the ligand binding sites of peroxisone proliferator activated receptors by GW9662. Biochemistry 2002 PMID: 12022867
- Seargent GW9662, a potent antaognist of PPARγ, inhibits growth of breast tumour cells and promotes the anticancer effects of the PPARγ agonist rosiglitazone, independently of PPARγ activation. Br.J.Pharmacol. 2004 PMID: 15533890
- Bendixen IL-4 inhibits osteoclast formation through a direct action on osteoclast precursors via peroxisome proliferator-activated receptor γ1. Proc.Natl.Acad.Sci.U.S.A. 2001 PMID: 11226258
Product Documents for GW 9662
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Product Specific Notices for GW 9662
For research use only
Related Research Areas
Citations for GW 9662
Customer Reviews for GW 9662 (3)
Have you used GW 9662?
Submit a review and receive an Amazon gift card!
$25/€18/£15/$25CAN/¥2500 Yen for a review with an image
$10/€7/£6/$10CAN/¥1110 Yen for a review without an image
Submit a review
Customer Images
-
Species: MouseAssay Type: In VitroCell Line/Tissue: Endothelial cellVerified Customer | Posted 12/05/2021GW 9662 at 2microM was used to test its effect on EC sprouting.
-
Species: MouseAssay Type: In VitroCell Line/Tissue: macrophageVerified Customer | Posted 09/24/2019Used this produce in mouse macrophages to inhibit ppar gamma at 1um. worked very well
-
Species: MouseAssay Type: In VitroCell Line/Tissue: HL-1 cardiomyocytesVerified Customer | Posted 12/10/2018HL-1 cardiomyocytes were incubated with GW 9662 (2 µM) for 30 min prior to addition of 15 µM 15d-PGJ2 for 30 min. Preincubation of cells with GW 9662 partially abolished activation of p42/44 MAPK, while Tesaglitazar and T 0070907 inhibited the activation completely.
There are no reviews that match your criteria.