admin 2021-08-05 09:04
GW9662A cell-permeable, selective and irreversible PPARγ antagonist (IC50 = 3.3 nM, 32 nM, and 2 碌M for PPARγ, PPARα, and PPARδ, respectively). Reported to covalently modify a cysteine residue in the bindin
g site of PPAR. At a concentration of 10 碌M, als