| Literature DB >> 35978694 |
Ana Flávia Borsoi1,2, Laura Manzoli Alice1, Nathalia Sperotto1, Alessandro Silva Ramos1, Bruno Lopes Abbadi1, Fernanda Souza Macchi Hopf1,3, Adilio da Silva Dadda1, Raoní S Rambo1, Rodrigo Braccini Madeira Silva1, Josiane Delgado Paz1,3, Kenia Pissinate1, Mauro Neves Muniz1, Christiano Ev Neves1,3, Luiza Galina1, Laura Calle González1,3, Marcia Alberton Perelló1, Alexia de Matos Czeczot1,3, Mariana Leyser4, Sílvia Dias de Oliveira3,4, Graziela de Araújo Lock5, Bibiana Verlindo de Araújo5, Teresa Dalla Costa5, Cristiano Valim Bizarro1,3, Luiz Augusto Basso1,2,3, Pablo Machado1,2,3.
Abstract
Using cycloalkyl and electron-donating groups to decrease the carbonyl electrophilicity, a novel series of 2-(quinoline-4-yloxy)acetamides was synthesized and evaluated as in vitro inhibitors of Mycobacterium tuberculosis (Mtb) growth. Structure-activity relationship studies led to selective and potent antitubercular agents with minimum inhibitory concentrations in the submicromolar range against drug-sensitive and drug-resistant Mtb strains. An evaluation of the activity of the lead compounds against a spontaneous qcrB mutant strain indicated that the structures targeted the cytochrome bc 1 complex. In addition, selected molecules inhibited Mtb growth in a macrophage model of tuberculosis infection. Furthermore, the leading compound was chemically stable depending on the context and showed good kinetic solubility, high permeability, and a low rate of in vitro metabolism. Finally, the pharmacokinetic profile of the compound was assessed after oral administration to mice. To the best of our knowledge, for the first time, a 2-(quinoline-4-yloxy)acetamide was obtained with a sufficient exposure, which may enable in vivo effectiveness and its further development as an antituberculosis drug candidate.Entities:
Year: 2022 PMID: 35978694 PMCID: PMC9376999 DOI: 10.1021/acsmedchemlett.2c00254
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.632