Name | Poseltinib |
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Description | Poseltinib, an orally active, selective and irreversible Bruton’s tyrosine kinase (BTK) inhibitor (IC50 =1.95 nM), with 0.3, 2.3 and 2.4-fold selectivity for BTK over BMX, TEC and TXK, respectively. Poseltinib can covalently bind to the active site (cysteine 481 residue) of BTK, and reveales potent inhibition of B cell receptor (BCR), Fc receptor (FcR), Toll-like receptor (TLR) mediated signaling[1]. |
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Related Catalog | |
Target |
IC50: 1.95 nM (BTK)[1] |
References |
Molecular Formula | C26H26N6O3 |
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Molecular Weight | 470.52 |