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Targeting energy metabolism in Mycobacterium tuberculosis (Mtb) is a new paradigm in the search for innovative anti-TB drugs. NADH:menaquinone oxidoreductase is a non-proton translocating type II NADH dehydrogenase (NDH-2) that is an essential enzyme in the respiratory chain of Mtb and is not found in mammalian mitochondria. Phenothiazines (PTZs) represent one of the most known class of NDH-2 inhibitors, but their use as anti-TB drugs is currently limited by the wide range of potentially serious off-target effects. In this work, we designed and synthesized a series of new PTZs by decorating the scaffold in an unconventional way, introducing various halogen atoms. By replacing the sulfur atom with selenium, a dibromophenoselenazine 20 was also synthesized. Among the synthesized poly-halogenated PTZs (HPTZs), dibromo and tetrachloro derivatives 9 and 11, along with the phenoselenazine 20, emerged with a better anti-TB profile than the therapeutic thioridazine (TZ). They targeted non-replicating Mtb, were bactericidal, and synergized with rifampin and bedaquiline. Moreover, their anti-TB activity was found to be related to the NDH-2 inhibition. Most important, they showed a markedly reduced affinity to dopaminergic and serotonergic receptors respect to the TZ. From this work emerged, for the first time, as the poly-halogenation of the PTZ core, while permitting to maintain good anti-TB profile could conceivably lead to fewer CNS side-effects risk, making more tangible the use of PTZs for this alternative therapeutic application. Copyright © 2020 Elsevier Masson SAS. All rights reserved.

Citation

Maria Giulia Nizi, Jenny Desantis, Yoshio Nakatani, Serena Massari, Maria Angela Mazzarella, Gauri Shetye, Stefano Sabatini, Maria Letizia Barreca, Giuseppe Manfroni, Tommaso Felicetti, Rowena Rushton-Green, Kiel Hards, Gniewomir Latacz, Grzegorz Satała, Andrzej J Bojarski, Violetta Cecchetti, Michal H Kolář, Jadwiga Handzlik, Gregory M Cook, Scott G Franzblau, Oriana Tabarrini. Antitubercular polyhalogenated phenothiazines and phenoselenazine with reduced binding to CNS receptors. European journal of medicinal chemistry. 2020 Sep 01;201:112420

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PMID: 32526553

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