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CWI1-2 is an IGF2BP2 inhibitor that binds IGF2BP2 and inhibits its interaction with m6A-modified target transcripts, induces apoptosis and differentiation, and shows promising anti-leukemic effects. In Vitro CWI1-2 (0-1 μM, 24 h) has good anti-leukemic efficacy. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Apoptosis AnalysisCell Line: MonoMac6, MOLM13 Concentration: 0-1 μM Incubation Time: 24 h Result: Induced significant cell differentiation and apoptosis in a concentration-dependent manner in IGF2BP2-high cells but not in IGF2BP2-low cells. Reduced Gln uptake and impaired mitochondrial function, resulting in reduced ATP production in AML cells. Significantly inhibited the colony-forming ability of MA9-induced leukemic mouse blasts and greatly impairs the self-renewal of LSC/LIC. In Vivo CWI1-2 (5 mg/kg, i.v., once daily, 7-10 days) can significantly delay the onset of leukemia and prolong the survival time of BMT recipient B6.SJL (CD45.1) mice without any loss in body weight . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid
中文名称
CWI1-2
英文名称
CWI1-2
中文别名
-
英文别名
-
CAS号
2408590-36-1
分子式
C22H17Cl3N6O3
分子量
519.77 g/mol
精确质量
≥98%
PSA
-
Logp
-
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CWI1-2 98% 10mg

CWI1-2 98% 10mg 麦克林 2408590-36-1,规格齐全,生产科研实验检测,科学材料数智化一站式易购平台。

品牌:麦克林
货号:C740525-10mg
级别: -
货期:30天
已售 75 件
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