Evain-Bana Emilie, Schiavo Lucie, Bour Christophe, Lanfranchi Don Antoine, Berardozzi Simone, Ghirga Francesca, Bagrel Denyse, Botta Bruno, Hanquet Gilles, Mori Mattia
a Pôle Chimie Et Physique Moléculaire, UMR CNRS 7565, Laboratoire Structure et Réactivite des Systèmes Moléculaires Complexes , Université de Lorraine , Metz , France.
b Ecole Européenne de Chimie, Polymères et Matériaux (ECPM), Laboratoire de Synthèse et Catalyze (UMR CNRS 7509) , Université de Strasbourg , Strasbourg , France.
J Enzyme Inhib Med Chem. 2017 Dec;32(1):113-118. doi: 10.1080/14756366.2016.1238364. Epub 2016 Oct 23.
The cell division cycle 25 phosphatases (CDC25A, B, and C; E.C. 3.1.3.48) are key regulator of the cell cycle in human cells. Their aberrant expression has been associated with the insurgence and development of various types of cancer, and with a poor clinical prognosis. Therefore, CDC25 phosphatases are a valuable target for the development of small molecule inhibitors of therapeutic relevance. Here, we used an integrated strategy mixing organic chemistry with biological investigation and molecular modeling to study novel quinonoid derivatives as CDC25 inhibitors. The most promising molecules proved to inhibit CDC25 isoforms at single digit micromolar concentration, becoming valuable tools in chemical biology investigations and profitable leads for further optimization. [Formula: see text].
细胞分裂周期25磷酸酶(CDC25A、B和C;酶学委员会编号3.1.3.48)是人类细胞中细胞周期的关键调节因子。它们的异常表达与各类癌症的发生和发展相关,且与不良临床预后有关。因此,CDC25磷酸酶是开发具有治疗相关性的小分子抑制剂的重要靶点。在此,我们采用了一种将有机化学与生物学研究及分子建模相结合的综合策略,来研究新型醌类衍生物作为CDC25抑制剂。最有前景的分子被证明能在个位数微摩尔浓度下抑制CDC25亚型,成为化学生物学研究中有价值的工具以及进一步优化的有利先导物。[化学式:见正文]