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is a potent and selective BET bromodomain inhibitor with Ki of <0
9a-pentamethyl-1-[(2S)-6-methyl-2-{[(2S
4T1 cells) treatment blocks the TGFβ-induced phosphorylation of Smad2 or Smad3 in a dose-dependent manner in 4T1 cells
Protease inhibitors: current status and future prospects
2ClH/c1-23-29(43-22-36-23)25-16-14-24(15-17-25)20-35-31(41)27-19-26(39)21-38(27)32(42)30(33(2
NH-3 Size:Contact [email protected] for quotation is a potent and selectiveNH 3 is an orally active, reversible thyroid hormone receptor (THR) antagonist with an IC50 of 55 nM. NH 3, a derivative of the selective thyromi metic GC 1, inhibits binding of thyroid hormones to their receptor and that inhibits cofactor recruitment. Product information CAS Number: 447415 26 1 Molecular Weight: 473. 52 Formula: C28H27NO6 Chemical Name: 2 [4 ({4 hydroxy 3 [2 (4 nitrophenyl)ethynyl] 5 (propan 2 yl)phenyl}methyl) 3, 5
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