Martínez Hoyos, MaríaMendoza Losana, Alfonso2023-11-102023-11-102016-05-08Martínez-Hoyos, M.,Mendoza-Losana, A. et al. (2016). Antitubercular drugs for an old target: GSK693 as a promising InhA direct inhibitor. EBioMedicine (Vol. 8), pp. 291-301.2352-3964https://hdl.handle.net/10016/38831Despite being one of the first antitubercular agents identified, isoniazid (INH) is still the most prescribed drug for prophylaxis and tuberculosis (TB) treatment and, together with rifampicin, the pillars of current chemotherapy. A high percentage of isoniazid resistance is linked to mutations in the pro-drug activating enzyme KatG, so the discovery of direct inhibitors (DI) of the enoyl-ACP reductase (InhA) has been pursued by many groups leading to the identification of different enzyme inhibitors, active against Mycobacterium tuberculosis (Mtb), but with poor physicochemical properties to be considered as preclinical candidates. Here, we present a series of InhA DI active against multidrug (MDR) and extensively (XDR) drug-resistant clinical isolates as well as in TB murine models when orally dosed that can be a promising foundation for a future treatment.eng© 2016 The Authors.Atribución-NoComercial-SinDerivadas 3.0 EspañaTuberculosisAntibioticInhABactericidalDrug discoverySingle-cell imagingCatalaseresearch articleMedicinahttps://doi.org/10.1016/j.ebiom.2016.05.006open access291301EBioMedicine8AR/0000030744