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Description: BTK inhibitor 27, compound 27 in the cited reference below, is a pyrrolo2, 3-dpyrimidine based BTK inhibitor with an IC50 of 0.11 nM for Btk and inhibits B cell activation in hWB with an IC50 of 2 nM. Btk is a tyrosine kinase dysregulated in several B-cell malignancies and autoimmune diseases, and this has given rise to a search for Btk inhibitors. Nevertheless, only one Btk inhibitor, ibrutinib, has been approved to date, although other compounds are currently being evaluated in clinical trials or in preclinal stages.
References: Expert Opin Ther Pat. 2017 Dec; 27(12):1305-1318.
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