BTK-IN-22 structure
|
Common Name | BTK-IN-22 | ||
---|---|---|---|---|
CAS Number | 2573048-10-7 | Molecular Weight | 454.52 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C26H26N6O2 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of BTK-IN-22BTK-IN-22 is a BTK inhibitor (IC50: 0.9 nM). BTK-IN-22 also inhibits BLX and BMX with IC50s of 1.4 and 1.2 nM respectively. BTK-IN-22 shows improved kinase selectivity compared to Ibrutinib (HY-10997)[1] |
Name | BTK-IN-22 |
---|
Description | BTK-IN-22 is a BTK inhibitor (IC50: 0.9 nM). BTK-IN-22 also inhibits BLX and BMX with IC50s of 1.4 and 1.2 nM respectively. BTK-IN-22 shows improved kinase selectivity compared to Ibrutinib (HY-10997)[1] |
---|---|
Related Catalog | |
In Vitro | BTK-IN-23 (Compound 2) 抑制 Jeko-1 细胞中 BTK 自磷酸化,IC50 值为 109 nM[1]. Western Blot Analysis[1] Cell Line: Jeko-1 cell Concentration: 0.01, 0.1, 1, 10 μM Incubation Time: 2 h Result: Inhibited BTK autophosphorylation. |
References |
Molecular Formula | C26H26N6O2 |
---|---|
Molecular Weight | 454.52 |