体内
铅(地质)
小分子
计算机科学
生物
生物信息学
化学
计算生物学
医学
数据科学
生物技术
生物化学
古生物学
作者
Mayako Michino,Tanweer A. Khan,Michael W. Miller,Yoshiyuki Fukase,Jérémie Vendôme,Carolina Adura,J. Fraser Glickman,Yiman Liu,Liling Wan,C. David Allis,Andrew W. Stamford,Peter T. Meinke,Louis M. Renzetti,Stacia Kargman,Nigel J. Liverton,David J. Huggins
标识
DOI:10.1021/acsmedchemlett.4c00016
摘要
Eleven-nineteen leukemia (ENL) is an epigenetic reader protein that drives oncogenic transcriptional programs in acute myeloid leukemia (AML). AML is one of the deadliest hematopoietic malignancies, with an overall 5-year survival rate of 27%. The epigenetic reader activity of ENL is mediated by its YEATS domain that binds to acetyl and crotonyl marks on histone tails and colocalizes with promoters of actively transcribed genes that are essential for leukemia. Prior to the discovery of TDI-11055, existing inhibitors of ENL YEATS showed in vitro potency, but had not shown efficacy in in vivo animal models. During the course of the medicinal chemistry campaign described here, we identified ENL YEATS inhibitor TDI-11055 that has an improved pharmacokinetic profile and is appropriate for in vivo evaluation of the ENL YEATS inhibition mechanism in AML.
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