||BMS-986142 is a potent and highly selective reversible BTK inhibitor (IC50: 0.5 nM).
||Evobrutinib, also known as M-2951 and MSC-2364447C, is a highly selective inhibitor o...
||PCI 29732 is a selective and irreversible Btk inhibitor with IC50 of 8.2 nM in a FRET...
||Acalabrutinib, also known as ACP-196, is an orally available inhibitor of Bruton’s ty...
||ONO-4059 analogue is an analogue of ONO-4059, which is a highly potent and selective ...
||LFM-A13（IC50=2.5 μM），a specific Bruton's tyrosine kinase (BTK), is more than 100-fold...
||BMS-777607 is a Met-related inhibitor for c-Met/Axl/Ron/Tyro3 (IC50: 3.9/1.1/1.8/4.3 ...
||Spebrutinib is an orally bioavailable, selective inhibitor of Bruton's agammaglobulin...
||CGI1746 is a potent and highly selective small-molecule Btk inhibitor with IC50 of 1....
||CNX-774 is a highly specific, irreversible, and orally active BTK inhibitor (IC50<1 n...
||RN486 is an effective and specific BTK inhibitor (IC50: 4 nM).
||Ibrutinib is an orally bioavailable, small-molecule inhibitor of Bruton's tyrosine ki...