AVL-292
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AVL-292 ??
- ??
- 1.322±0.06 g/cm3(Predicted)
- ?? ??
- Store at -20°C
- ???
- ≥21.15 mg/mL in DMSO; insoluble in H2O; ≥4.9 mg/mL in EtOH with gentle warming and ultrasonic
- ??? ??
- ??
- ??? ??
- ??? ??
- ?? ?? (pKa)
- 13.22±0.70(Predicted)
- ??
- White to khaki
- CAS ??????
- 1202757-89-8
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AVL-292 C??? ??, ??, ??
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Bruton’s tyrosine kinase (BTK) is a non-receptor tyrosine kinase involved in signal transduction pathways regulating the proliferation, activation, and differentiation of B cells. AVL-292 is an orally available, selective, and irreversible inhibitor of BTK (IC50 = 0.5 nM in vitro in B cell lymphoma cell lines) that targets and covalently binds to BTK at cysteine-481, thereby preventing its activity. AVL-292 has been shown to inhibit osteoclast function and to reduce osteoclast-stimulated proliferation of multiple myeloma cells in animal models of rheumatoid arthritis and multiple sclerosis, both of which are diseases where B cells play an important role. In clinical trials, AVL-292 has demonstrated therapeutic significance in the treatment of both B cell-related cancers (e.g., non-Hodgkin’s lymphoma and B cell chronic lymphocytic leukemia) and autoimmune diseases (e.g., rheumatoid arthritis).[Cayman Chemical]AVL-292 ?? ?? ? ???
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AVL-292 ?? ??
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