| Literature DB >> 33668389 |
Ana Flávia Borsoi1,2, Josiane Delgado Paz1,3, Kenia Pissinate1, Raoní Scheibler Rambo1, Víctor Zajaczkowski Pestana1, Cristiano Valim Bizarro1,3, Luiz Augusto Basso1,2,3, Pablo Machado1,2,3.
Abstract
Tuberculosis (TB) has been described as a global health crisis since the second half of the 1990s. Mycobacterium tuberculosis (Mtb), the etiologic agent of TB in humans, is a very successful pathogen, being the main cause of death in the population among infectious agents. In 2019, it was estimated that around 10 million individuals were contaminated by this bacillus and about 1.2 million succumbed to the disease. In recent years, our research group has reported the design and synthesis of quinoline derivatives as drug candidates for the treatment of TB. These compounds have demonstrated potent and selective growth inhibition of drug-susceptible and drug-resistant Mtb strains. Herein, a new synthetic approach was established providing efficient and rapid access (15 min) to a series of 4-alkoxy-6-methoxy-2-methylquinolines using ultrasound energy. The new synthetic protocol provides a simple procedure utilizing an open vessel system that affords the target products at satisfactory yields (45-84%) and elevated purities (≥95%). The methodology allows the evaluation of a larger number of molecules in assays against the bacillus, facilitating the determination of the structure-activity relationship with a reduced environmental cost.Entities:
Keywords: antituberculosis drug discovery; heterocyclic synthesis; new methods; sonochemistry
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Year: 2021 PMID: 33668389 PMCID: PMC7956363 DOI: 10.3390/molecules26051215
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411