CM-272 是一流的、强效、选择性、底物竞争性和可逆的双重 G9a/DNA 甲基转移酶 (DNMTs) 抑制剂，具有抗肿瘤活性。 CM-272 抑制 G9a、DNMT1、DNMT3A、DNMT3B 和 GLP，IC50 分别为 8 nM、382 nM、85 nM、1200 nM 和 2 nM。 CM-272 抑制细胞增殖并促进细胞凋亡，诱导 IFN 刺激的基因和免疫原性细胞死亡。
货号:ajcx11138
CAS:1846570-31-7
分子式:C28H38N4O3
分子量：478.63
溶解度:DMF: 30 mg/ml,DMSO: 30 mg/ml,Ethanol: 30 mg/ml,Ethanol:PBS (pH 7.2) (1:6): 0.15 mg/ml
纯度：98%
存储：Store at -20°C
库存：现货

Background:

 CM-272 is a first-in-class reversible dual inhibitor against G9a and DNMTs with IC50 values of 8 nM and 382 nM, respectively [1].

 G9a is a histone methyltransferase that is overexpressed in many tumors. Inhibition of G9a expression reduces cancer cell proliferation, delays disease progression and inhibits tumor metastasis. G9a interacts with DNA methyltransferase-1 (DNMT1) to coordinate DNA and histone methylation during cell division promoting transcriptional silencing of target genes. Reduction of both DNA and H3K9 methylation levels leads to reactivation of tumor suppressor genes and inhibits cancer cell proliferation [1].

 CM-272 is a first-in-class reversible and substrate-competitive dual inhibitor of G9a and DNMTs. In ALL, AML and DLBCL-derived cell lines, CM-272 reduced DNA methylation in the promoter region of specific tumor suppressor genes. CM-272 also inhibited cell proliferation, blocked cell cycle progression and induced apoptosis in a dose-dependent way [1].

 In immunodeficient Rag2-/-γc-/- mice injected i.v. with ALL-derived CEMO cells, CM-272 significantly increased overall survival (OS) in mice (median OS; 92±5.7 days versus 55±10.5 days; P=0.0009) without significant weight loss. In immunodeficient Rag2-/-γc-/- mice injected i.v. with AML-derived MV4-11 cells, CM-272 also prolonged OS in mice. CM-272 exerted a potent anti-tumour activity in vivo against different types of haematological malignancies by inhibiting the methyltransferase activity of both G9a/GLP and DNMTs [1].

 

参考文献:

[1]. San José-Enériz E, Agirre X, Rabal O, et al. Discovery of first-in-class reversible dual small molecule inhibitors against G9a and DNMTs in hematological malignancies. Nat Commun. 2017 May 26;8:15424. doi: 10.1038/ncomms15424.