Cs1 fto抑制剂
Web10 月 14 日,浙江大学医学院干细胞与再生医学中心张进课题组与清华大学药学院胡泽平课题组合作在 Nature Metabolism 上发表题为 “Metabolic remodeling during early mouse embryo development” 的文章。. 该文章系统描绘了小鼠着床前胚胎发育过程中的代谢重塑过程,发现关键代谢物 L-2-羟基戊二酸( L-2-hydroxyglutarate ... WebJul 19, 2024 · cs1和cs2是高效的fto抑制剂,在体外具有很强的抗白血病作用,与之前报道的两种fto抑制剂(fb23-2和mo-i-500)相比,cs1和cs2在抑制aml细胞活力方面表现出更 …
Cs1 fto抑制剂
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http://probechem.com/products_FTOinhibitorCS1.html Webfto fto inhibitor Prior art date 2024-02-20 Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.) Pending Application number CN202410192643.0A Other languages English (en) Inventor 夏来新 郑新瑶 李源
Web该化合物选择性抑制aml细胞中fto的去甲基化功能,上调aml关键基因mrna上m6a修饰,增加抑癌蛋白质例如asb2和rara的丰度,降低促癌蛋白质例如myc和cebpa的丰度,从而抑 … WebJan 3, 2024 · The effort to cajole and bully elected officials in his own party — which some legal experts said could be prosecuted under Georgia law — was a remarkable act by a …
WebIt turns out that modifying FTO or using small molecules to inhibit FTO interrupts the supply chain that enables cancer to develop and progress. Studies showed that treatment with a relatively low dose of CS1 or CS2 (5 mg/kg/day 10 times every other day) could, at the very least, double the median survival in mouse models with AML. WebMar 27, 2024 · 作者:X-MOL 2024-03-27. 组蛋白去甲基化修饰是表观遗传调控的一种重要方式。赖氨酸特异性去甲基化酶1(Lysine specific demethylase 1, LSD1)是一种黄素腺嘌呤二核苷酸(FAD)依赖的去甲基化酶,属于胺氧化酶家族成员,其能够催化单甲基化或二甲基化的H3K4及H3K9的去甲基化过程。
WebBiological Activity. FTO inhibitor CS1 (NSC 337766) is a potent, selective small-molecule inhibitor of m6A demethylase FTO, inhibits m6A demethylation with IC50 of 142.6 nM in vitro (cell-free) assays. CS1 is highly efficacious FTO inhibitors with potent anti-leukemic efficacy againsta panel of leukemia cell lines with high FTO expression in ...
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