M6191

GW9662

>98% (HPLC)

• Sinónimos: 2-Chloro-5-nitro-N-phenylbenzamide
• Fórmula empírica (notación de Hill): C₁₃H₉ClN₂O₃
• Número de CAS: 22978-25-2
• Peso molecular: 276.68
• MDL number: MFCD01215270
• UNSPSC Code: 51111800
• PubChem Substance ID: 24278560
• NACRES: NA.77

Propiedades

• assay: >98% (HPLC)
• form: powder
• color: white
• solubility: DMSO: 26 mg/mL; H₂O: insoluble
• storage temp.: 2-8°C
• SMILES string: [O-][N+](=O)c1ccc(Cl)c(c1)C(=O)Nc2ccccc2
• InChI: 1S/C13H9ClN2O3/c14-12-7-6-10(16(18)19)8-11(12)13(17)15-9-4-2-1-3-5-9/h1-8H,(H,15,17)
• InChI key: DNTSIBUQMRRYIU-UHFFFAOYSA-N
• Gene Information: human ... PPARG(5468)

Descripción

Application

GW9662 has been used as a peroxisome proliferator activated receptor γ (PPARγ) antagonist in human pluripotent stem cells, in phenylephrine stimulated cardiomyocytes and to inhibit the protective effect of telmisartan pheochromocytoma, PC12 cells.

Biochem/physiol Actions

GW9662 (2-chloro-5-nitrobenzanilide) binds to the ligand binding site of the peroxisome proliferator activated receptor γ (PPARγ) and results in the inhibition of adipocyte differentiation. It favors cell growth suppression in breast cancer cell lines even in the presence of PPARγ agonist rosiglitazone. It stimulates M2c macrophages differentiation and triggers growth arrest-specific 6 (Gas6) expression. GW9662 co treatment with other PPARγ ligands elicits antiproliferative effects on the glioblastoma stem cells and could be a potent therapeutic agent.

GW9662 is an irreversible PPARγ antagonist. GW9662 inhibits connective tissue growth factor and activation of CD36 by IL-4.

Features and Benefits

This compound is featured on the Nuclear Receptors (PPARs) page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Legal Information

Sold for research purposes only, under agreement from Glaxo­Smith­Kline

Información de seguridad

• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3