Chemical Structure : BMS-986195
CAS No.: 1912445-55-6
Catalog No.: PC-63295Not For Human Use, Lab Use Only.
BMS-986195 (Branebrutinib) is a novel potent, selective, covalent, irreversible inhibitor of Bruton’s tyrosine kinase (BTK) with IC50 of 0.1 nM.
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---|---|---|---|
1 mg (Free Sample) | $18 | In stock | |
5 mg | $128 | In stock | |
10 mg | $198 | In stock | |
25 mg | $348 | In stock | |
50 mg | $548 | In stock | |
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BMS-986195 (Branebrutinib) is a novel potent, selective, covalent, irreversible inhibitor of Bruton’s tyrosine kinase (BTK) with IC50 of 0.1 nM.
BMS-986195 (Branebrutinib) displays >5,000-fold selective over all kinases outside of the Tec family, and selectivity ranges 9- to 1010-fold within the Tec family.
BMS-986195 (Branebrutinib) potently inhibits antigen-dependent interleukin-6 production, CD86 expression and proliferation in B cells (IC50<1 nM).
BMS-986195 (Branebrutinib) demonstrates robust efficacy in murine models of RA including CIA and CAIA, protecting against clinically evident disease, histologic joint damage and bone mineral density loss.
M.Wt | 370.428 | |
Formula | C20H23FN4O2 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
(S)-4-(3-(but-2-ynamido)piperidin-1-yl)-5-fluoro-2,3-dimethyl-1H-indole-7-carboxamide |
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