1271809-52-9Relevant academic research and scientific papers
Optimization of novel reversible Bruton's tyrosine kinase inhibitors identified using Tethering-fragment-based screens
Hopkins, Brian T.,Bame, Eris,Bell, Noah,Bohnert, Tonika,Bowden-Verhoek, Jon K.,Bui, Minna,Cancilla, Mark T.,Conlon, Patrick,Cullen, Patrick,Erlanson, Daniel A.,Fan, Junfa,Fuchs-Knotts, Tarra,Hansen, Stig,Heumann, Stacey,Jenkins, Tracy J.,Marcotte, Douglas,McDowell, Bob,Mertsching, Elisabeth,Negrou, Ella,Otipoby, Kevin L.,Poreci, Urjana,Romanowski, Michael J.,Scott, Daniel,Silvian, Laura,Yang, Wenjin,Zhong, Min
, p. 2905 - 2913 (2019)
Since the approval of ibrutinib for the treatment of B-cell malignancies in 2012, numerous clinical trials have been reported using covalent inhibitors to target Bruton's tyrosine kinase (BTK) for oncology indications. However, a formidable challenge for
BRUTON'S TYROSINE KINASE INHIBITORS
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Page/Page column 130; 131, (2011/04/14)
The present invention provides compounds useful as inhibitors of Btk, compositions thereof, and methods of using the same.
