Cas No.: | 2408590-37-2 |
SMILES: | Cl.C(/C1C=C(Cl)C=CC=1O)=N/N=C(/N/N=C/C1C=C(Cl)C=CC=1O)\N/N=C/C1C=C(Cl)C=CC=1O |
Formula: | C22H18Cl4N6O3 |
M.Wt: | 556.228720188141 |
Purity: | >98% |
Sotrage: | 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
Description: | CWI1-2 hydrochloride is an inhibitor of IGF2BP2 that binds IGF2BP2 and inhibits its interaction with m6A-modified target transcripts, induces apoptosis and differentiation, and shows promising anti-leukemic effects. |
In Vivo: | CWI1-2(5 mg/kg,i.v.,每日一次,7-10天)hydrochloride 可显着延缓 BMT 受体 B6.SJL(CD45.1)小鼠白血病的发生和存活时间,体重无明显影响 [1]。 |
In Vitro: | CWI1-2 (0-1 μM, 24 h) hydrochloride 具有良好的抗白血病功效[1]。 Apoptosis Analysis[1] Cell 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. |
References: | [1]. Hengyou Weng, et al. The m6A reader IGF2BP2 regulates glutamine metabolism and represents a therapeutic target in acute myeloid leukemia. Cancer Cell. 2022 Dec 12;40(12):1566-1582.e10. |