PPARγ

Peroxisome proliferator-activated receptor gamma (PPARγ ) is a member of the nuclear receptor family of ligand-activated transcription factors that heterodimerize with the retinoic X receptor (RXR) to regulate gene expression.

Products for PPARγ - Page 2

  1. Cat.No. Product Name Information/Activity
  2. BCC1573 FH535 FH535 is an inhibitor of Wnt/β-catenin and PPAR, with anti-tumor activities. FH535 chemical structure
  3. BCC2260 GW9662 GW9662 is a potent and selective PPARγ antagonist with an IC50 of 3.3 nM, showing 10 and 1000-fold selectivity over PPARα and PPARδ, respectively. GW9662 chemical structure
  4. BCC7243 SR 202 Mifobate (SR-202) is a potent and specific PPARγ antagonist. Mifobate (SR-202) selectively inhibits Thiazolidinedione (TZD)-induced PPARγ transcriptional activity (IC50=140 μM). Mifobate (SR-202) does not affect basal or ligand-stimulated transcriptional activity of PPARα, PPARβ, or the farnesoid X receptor (FXR). Mifobate (SR-202) shows antiobesity and antidiabetic effects. SR 202 chemical structure
  5. BCC2261 T0070907 T0070907 is a potent PPARγ antagonist with a Ki of 1 nM. T0070907 chemical structure
  6. BCN5499 Genistein Genistein, a soy isoflavone, is a multiple tyrosine kinases (e.g., EGFR) inhibitor which acts as a chemotherapeutic agent against different types of cancer, mainly by altering apoptosis, the cell cycle, and angiogenesis and inhibiting metastasis. Genistein chemical structure
  7. BCC6166 SR 1664 1338259-05-4 SR 1664 chemical structure

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