Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford, OX1 3TA, UK.
Structural Genomics Consortium and Target Discovery Institute, Nuffield Department of Medicine, University of Oxford, Roosevelt Drive, Oxford, OX3 7DQ, UK.
Angew Chem Int Ed Engl. 2017 Dec 4;56(49):15555-15559. doi: 10.1002/anie.201706788. Epub 2017 Nov 7.
Histone lysine demethylases (KDMs) are of critical importance in the epigenetic regulation of gene expression, yet there are few selective, cell-permeable inhibitors or suitable tool compounds for these enzymes. We describe the discovery of a new class of inhibitor that is highly potent towards the histone lysine demethylases KDM2A/7A. A modular synthetic approach was used to explore the chemical space and accelerate the investigation of key structure-activity relationships, leading to the development of a small molecule with around 75-fold selectivity towards KDM2A/7A versus other KDMs, as well as cellular activity at low micromolar concentrations.
组蛋白赖氨酸去甲基酶(KDMs)在基因表达的表观遗传调控中至关重要,但目前针对这些酶的选择性、细胞通透的抑制剂或合适的工具化合物还很少。我们描述了一类新型抑制剂的发现,这类抑制剂对组蛋白赖氨酸去甲基酶 KDM2A/7A 具有很高的活性。采用模块化合成方法来探索化学空间并加速对关键结构-活性关系的研究,从而开发出一种小分子化合物,其对 KDM2A/7A 的选择性约为其他 KDMs 的 75 倍,在低微摩尔浓度下具有细胞活性。