Ivacaftor-D9 Size:Contact [email protected] for quotation an effect which could be

an effect which could be blocked by the DA1-selective antagonist Sch 23390

is a potent and selective and orally active PRMT5 inhibitor with a half-maximal inhibitory concentration (IC50) of 22 nM and broad selectivity against a panel of other histone methyltransferases

induces apoptosis and suppresses centroblast population

TEPP-46 inhibits LPS-induced Hif-1α and IL-1β

TK216 is a potent inhibitor targeting E26 transformation specific (ETS) factors via blocking the protein-protein interaction with RNA helicases

Ivacaftor-D9 Size:Contact [email protected] for quotation an effect which could beIvacaftor D9 (CTP 656) is a potent CFTR modulator and exhibits an EC50 value of 255 nM for CFTR potentiation in G551D F508del HBE Cells. Ivacaftor D9 acts as an orally active and improved deuterated Ivacaftor analog for cystic fibrosis research. Product information CAS Number: 1413431 07 8 Molecular Weight: 401. 55 Formula: C24H28N2O3 Chemical Name: N {2 tert butyl 5 hydroxy 4 [2 (H)methyl(1,1,1,3,3,3 H)propan 2 yl]phenyl} 4 oxo 1,4 dihydroquinoline 3