Name | Pacritinib hydrochloride |
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Description | Pacritinib hydrochloride is a potent inhibitor of both wild-type JAK2 (IC50=23 nM) and JAK2V617F mutant (IC50=19 nM). Pacritinib hydrochloride also inhibits FLT3 (IC50=22 nM) and its mutant FLT3D835Y (IC50=6 nM). Pacritinib hydrochloride can be used for the research of acute myeloid leukemia (AML) and myelofibrosis (MF)[1][2][3]. |
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Related Catalog | |
Target |
JAK2V617F:19 nM (IC50) JAK3:520 nM (IC50) JAK1:1280 nM (IC50) JAK2wt:23 nM (IC50) Tyk2:50 nM (IC50) |
References |
Molecular Formula | C28H32N4O3.xClH |
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