de Faria, Catarina Frazão, Moreira, Tânia, Lopes, Pedro, Costa, Henrique, Krewall, Jessica R., Barton, Callie M., Santos, Susana, Goodwin, Douglas, Machado, Diana, Viveiros, Miguel, Machuqueiro, Miguel, and Martins, Filomena
Isoniazid (INH) is one of the two most effective first-line antitubercular drugs and is still used at the present time as a scaffold for developing new compounds to fight TB. In a previous study, we have observed that an INH derivative, an hydrazide N ′-substituted with a C 10 acyl chain, was able to counterbalance its smaller reactivity with a higher membrane permeability. This resulted in an improved performance against the most prevalent Mycobacterium tuberculosis (Mtb) resistant strain (S315T), compared to INH. In this work, we have designed two new series of INH derivatives (alkyl hydrazides and hydrazones) with promising in silico properties, namely membrane permeabilities and spontaneous IN* radical formation. The kinetics, cytotoxicity, and biological activity evaluations confirmed the in silico predictions regarding the very high reactivity of the alkyl hydrazides. The hydrazones, on the other hand, showed very similar behavior compared to INH, particularly in biological tests that take longer to complete, indicating that these compounds are being hydrolyzed back to INH. Despite their improved membrane permeabilities, the reactivities of these two series are too high, impairing their overall performance. Nevertheless, the systematic data gathered about these compounds have showed us the need to find a balance between lipophilicity and reactivity, which is paramount to devise better INH-based derivatives aimed at circumventing Mtb resistance. [Display omitted] • Two series of isoniazid derivatives were designed as potential antitubercular drugs. • These derivatives showed promising in silico membrane permeabilities and reactivities. • Alkyl hydrazides decompose faster than the KatG-catalyzed reaction impairing activity. • Hydrazones hydrolyze back to INH mimicking its overall behavior. • A balance between lipophilicity and reactivity is key to overcome Mtb resistance. [ABSTRACT FROM AUTHOR]