Denora Nunzio, Margiotta Nicola, Laquintana Valentino, Lopedota Angela, Cutrignelli Annalisa, Losacco Maurizio, Franco Massimo, Natile Giovanni
Dipartimento di Farmacia-Scienze del Farmaco, Università degli Studi di Bari "A. Moro" , via Orabona 4, 70125 Bari, Italy.
Dipartimento di Chimica, Università degli Studi di Bari "A. Moro" , via Orabona 4, 70125 Bari, Italy.
ACS Med Chem Lett. 2014 Mar 30;5(6):685-9. doi: 10.1021/ml5000788. eCollection 2014 Jun 12.
The 18-kDa translocator protein (TSPO) is overexpressed in many types of cancers and is also abundant in activated microglial cells occurring in inflammatory neurodegenerative diseases. Thus, TSPO has become an extremely attractive subcellular target not only for imaging disease states overexpressing this protein, but also for a selective mitochondrial drug delivery. In this work we report the synthesis, the characterization, and the in vitro evaluation of a new TSPO-selective ligand, 2-(8-(2-(bis(pyridin-2-yl)methyl)amino)acetamido)-2-(4-chlorophenyl)H-imidazo[1,2-a]pyridin-3-yl)-N,N-dipropylacetamide (CB256), which fulfils the requirements for a bifunctional chelate approach. The goal was to provide a new TSPO ligand that could be used further to prepare coordination complexes of a metallo drug to be used in diagnosis and therapy. However, the ligand itself proved to be a potent tumor cell growth inhibitor and DNA double-strand breaker.
18 kDa转位蛋白(TSPO)在多种癌症中过表达,在炎症性神经退行性疾病中活化的小胶质细胞中也大量存在。因此,TSPO不仅已成为用于对过表达该蛋白的疾病状态进行成像的极具吸引力的亚细胞靶点,还成为用于选择性线粒体药物递送的靶点。在这项工作中,我们报告了一种新型TSPO选择性配体2-(8-(2-(双(吡啶-2-基)甲基)氨基)乙酰胺基)-2-(4-氯苯基)H-咪唑并[1,2-a]吡啶-3-基)-N,N-二丙基乙酰胺(CB256)的合成、表征及体外评价,该配体满足双功能螯合方法的要求。目标是提供一种新的TSPO配体,可进一步用于制备用于诊断和治疗的金属药物配位络合物。然而,该配体本身被证明是一种有效的肿瘤细胞生长抑制剂和DNA双链断裂剂。