Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Spebrutinib besylate (AVL-292 benzenesulfonate; CC-292 besylate) is a Btk kinase activity inhibitor (IC50<0.5 nM, Kinact/Ki=7.69×104 M-1s-1s).
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
25 mg | 6-8 weeks | $ 1,520.00 | |
50 mg | 6-8 weeks | $ 1,980.00 | |
100 mg | 6-8 weeks | $ 2,500.00 |
Description | Spebrutinib besylate (AVL-292 benzenesulfonate; CC-292 besylate) is a Btk kinase activity inhibitor (IC50<0.5 nM, Kinact/Ki=7.69×104 M-1s-1s). |
Targets&IC50 | BTK:<0.5 nM |
In vitro | Spebrutinib also less potently inhibits Yes, c-Src, Brk, Lyn, and Fyn with IC50s of 723 nM, 1.729 μM, 2.43 μM, 4.4 μM, and 7.15 μM, rspectively. Spebrutinib (CC-292) is a covalent, highly selective, orally active inhibitor of Btk with IC50 value of 0.5 nM. The concentration at which Spebrutinib inhibits 90% of Btk activity in Ramos cells is 35 nM while the concentration of Spebrutinib required for 90% occupancy of Btk is 39 nM[1]. Extensive analysis has revealed that the EC50 of Btk occupancy from a Spebrutinib dose-response in Ramos cells (EC50=6 nM) correlated directly with the cellular EC50 of Btk kinase inhibition with Spebrutinib (EC50=8 nM). |
Synonyms | CC-292 (besylate), AVL-292 (benzenesulfonate) |
Molecular Weight | 581.62 |
Formula | C28H28FN5O6S |
CAS No. | 1360053-81-1 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
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Spebrutinib besylate 1360053-81-1 Angiogenesis Tyrosine Kinase/Adaptors BTK benzenesulfonate AVL 292 AVL292 CC 292 CC292 CC-292 (besylate) besylate CC-292 AVL-292 AVL-292 (benzenesulfonate) inhibitor inhibit