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首页-小分子抑制剂&激动剂-JAK/STAT Signaling-JAK-Flonoltinib maleate
Flonoltinib maleate

Chemical Structure : Flonoltinib maleate

CAS No.: 2568842-57-7

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Flonoltinib maleate

货号: PC-38006Not For Human Use, Lab Use Only.

Flonoltinib maleate is a potent, highly selective, dual JAK2/FLT3 inhibitor with IC50 of 0.8, 1.4, and 15 nM for JAK2, JAK2V617F, and FLT3, respectively.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

Flonoltinib maleate is a potent, highly selective, dual JAK2/FLT3 inhibitor with IC50 of 0.8, 1.4, and 15 nM for JAK2, JAK2V617F, and FLT3, respectively.
Flonoltinib displays 650-900 folds more selectivity to JAK2 than JAK1 and JAK3, and -80 folds greater selectivity for JAK2 over TYK2.
Flonoltinib binds to JH1, JH2, and JH2V617F of JAK2 with KD values of 20.9, 3.14 and 5.21 uM, respectively, demonstrates high inhibitory activity and selectivity for JAK2 JH2 protein.
Flonoltinib inhibits GM-CSF-induced p-STAT5, which involve JAK2/JAK2 signaling with IC50 of 0.12 uM, but not IFN-α-induced p-STAT1 (IC50>5 uM).|
Flonoltinib exhibits anti-proliferative IC50 values of <0.5 uM on JAK2V617F mutant cell lines, with stronger anti-proliferative activity in mutant (Ba/F3-JAK2V617F) cell lines (IC50=0.2 uM) than wild-type cells (Ba/F3-JAK2WT, IC50= 0.39 uM).
Flonoltinib also inhibits FLT3 mutant tumor cell lines with IC50 <0.1 uM.
Flonoltinib (15 and 30 mg/kg) demonstrates robust antitumor activity in Ba/F3-JAK2 V617F disease model. Flonoltinib also shows efficacy against JAK2V617F bone marrow transplantation (BMT) mouse model of myelofibrosis in vivo, orally active.

物理化学性质&存储条件

分子量 583.665
分子式 C29H38FN7O5
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO
Chemical Name/SMILES

2-((1-(2-fluoro-4-((4-(1-isopropyl-1H-pyrazol-4-yl)-5-methylpyrimidin-2-yl)amino)phenyl)piperidin-4-yl)(methyl)amino)ethan-1-ol maleate

参考文献

1. Hu M, et al. Blood Cancer J. 2022 Mar 7;12(3):37.

2. Zhu J, et al. Biomed Pharmacother. 2021 May;137:111373.

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