| Literature DB >> 24944744 |
Nunzio Denora1, Nicola Margiotta2, Valentino Laquintana1, Angela Lopedota1, Annalisa Cutrignelli1, Maurizio Losacco2, Massimo Franco1, Giovanni Natile2.
Abstract
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.Entities:
Keywords: DNA cleavage; PBR; TSPO; apoptosis; bifunctional chelate approach
Year: 2014 PMID: 24944744 PMCID: PMC4060941 DOI: 10.1021/ml5000788
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345