Detalle Publicación

Antikinetoplastid SAR study in 3-nitroimidazopyridine series: Identification of a novel non-genotoxic and potent anti-T.b. brucei hitcompound with improved pharmacokinetic properties

Autores: Fersing, C. ; Boudot, C. ; Paoli-Lombardo, R.; Primas, N. ; Pinault, E. ; Hutter, S. ; Castera-Ducros, C. ; Kabri, Y. ; Pedron, J. ; Bourgeade-Delmas, S. ; Sournia-Saquet, A.; Stigliani, J. L.; Valentin, A. ; Azqueta Oscoz, Amaya; Muruzábal Gambarte, Damián; Destere, A. ; Wyllie, S. ; Fairlamb, A. H.; Corvaisier, S. ; Since, M. ; Malzert-Freon, A. ; Di Giorgio, C. ; Rathelot, P.; Azas, N.; Courtioux, B. ; Vanelle, P.; Verhaeghe, P. (Autor de correspondencia)
ISSN: 0223-5234
Volumen: 206
Número: 112668
Fecha de publicación: 2020
To study the antikinetoplastid 3-nitroimidazo[1,2-alpyridine pharmacophore, a structure-activity relationship study was conducted through the synthesis of 26 original derivatives and their in vitro evaluation on both Leishmania spp and Tiypanosoma brucei brucei. This SAR study showed that the antitrypanosomal pharmacophore was less restrictive than the antileishmanial one and highlighted positions 2, 6 and 8 of the imidazopyridine ring as key modulation points. None of the synthesized compounds allowed improvement in antileishmanial activity, compared to previous hit molecules in the series. Nevertheless, compound 8, the best antitrypanosomal molecule in this series (EC50 = 17 nM, SI = 2650 & E degrees = -0.6 V), was not only more active than all reference drugs and previous hit molecules in the series but also displayed improved aqueous solubility and better in vitro pharmacokinetic characteristics: good microsomal stability (T-1/2 > 40 min), moderate albumin binding (77%) and moderate permeability across the blood brain barrier according to a PAMPA assay. Moreover, both micronucleus and comet assays showed that nitroaromatic molecule 8 was not genotoxic in vitro. It was evidenced that bioactivation of molecule 8 was operated by T. b. brucei type 1 nitroreductase, in the same manner as fexinidazole. Finally, a mouse pharmacokinetic study showed that 8 displayed good systemic exposure after both single and repeated oral administrations at 100 mg/kg (NOAEL) and satisfying plasmatic half-life (T-1/2 = 7.7 h). Thus, molecule 8 appears as a good candidate for initiating a hit to lead drug discovery program. (C) 2020 Elsevier Masson SAS. All rights reserved.