FB23-2 是一种有效、选择性的 mRNA N6- 甲基腺嘌呤脱甲基酶 FTO 抑制剂，IC50 值为 2.6 μM。
CAS：2243736-45-8
分子式：C18H15Cl2N3O3
分子量：392.24
纯度：98%
存储：Store at -20°C

Background:

FB23-2 is a potent and selective inhibitor of mRNA N6-methyladenosine (m6A) demethylase FTO, with an IC50 of 2.6 μM[1]. IC50: 2.6 μM (FTO)[1]

FB23-2 dramatically suppresses proliferation and promotes the differentiation/apoptosis of human acute myeloid leukemia (AML) cell line cells and primary blast AML cells[1]. FB23 inhibits the proliferation of NB4 and MONOMAC6 cells, with IC50 values of 0.8 μM and 1.5 μM[1].

FB23-2 significantly inhibits the progression of human AML cell lines and primary cells in xeno-transplanted mice[1].

[1]. Huang Y, et al. Small-Molecule Targeting of Oncogenic FTO Demethylase in Acute Myeloid Leukemia. Cancer Cell. 2019 Apr 15;35(4):677-691.e10.