CAS NO: | 936091-26-8 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
1 g | 电议 |
2 g | 电议 |
5 g | 电议 |
10 g | 电议 |
50 g | 电议 |
生物活性 |
Fedratinib (TG-101348) is a potent, selective, ATP-competitive and orally activeJAK2inhibitor withIC50s of 3 nM for bothJAK2andJAK2V617F kinase. Fedratinib shows 35- and 334-fold selectivity overJAK1andJAK3, respectively. Fedratinib inducescancercellapoptosisand has the potential for myeloproliferative disorders research[1][2]. |
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IC50& Target |
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体外研究 (In Vitro) |
Fedratinib (TG101348) inhibits proliferation of a human erythroblast leukemia (HEL) cell line that harbors the JAK2V617F mutation, as well as a murine pro-B cell line expressing human JAK2V617F (Ba/F3 JAK2V617F), with an IC50value of approximately 300 nM for either line. Proliferation of parental Ba/F3 cells was inhibited to a comparable level, with an IC50value of ~420 nM[1].
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体内研究 (In Vivo) |
Fedratinib (TG101348; 60-120 mg/kg; oral gavage; twice daily; for 42 days; C57Bl/6 mice) trewatment shows a dose-dependent reduction in polycythemia and a marked dose-dependent reduction in splenomegaly of treated animals[1].
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Clinical Trial |
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分子量 |
524.68 |
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性状 |
Solid |
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Formula |
C27H36N6O3S |
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CAS 号 |
936091-26-8 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 125 mg/mL(238.24 mM;Need ultrasonic)
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In Vivo:
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