Please use this identifier to cite or link to this item: http://hdl.handle.net/1843/72108
Type: Artigo de Periódico
Title: Synthesis of novel 1,2,3-triazole derivatives of isocoumarins and 3,4-dihydroisocoumarin with potential antiplasmodial activity in vitro
Authors: Lucas da Silva Santos
Matheus Fillipe Langanke de Carvalho
Ana Claudia de Souza Pinto
Amanda Luisa da Fonseca
Julio César Dias Lopes
Fernando de Pilla Varotti
Rossimiriam Pereira de Freitas
Rosemeire Brondi Alves
Abstract: Background: Malaria greatly affects the world health, having caused more than 228 million cases only in 2018. The emergence of drug resistance is one of the main problems in its treatment, demonstrating the need for the development of new antimalarial drugs. Objective: Synthesis and in vitro antiplasmodial evaluation of triazole compounds derived from isocoumarins and a 3,4-dihydroisocoumarin. Methods: The compounds were synthesized in 4 to 6-step reactions with the formation of the triazole ring via the Copper(I)-catalyzed 1,3-dipolar cycloaddition between isocoumarin or 3,4-dihydroisocoumarin azides and terminal alkynes. This key reaction provided compounds with an unprecedented connection of isocoumarin or 3,4-dihydroisocoumarin and the 1,2,3-triazole ring. The products were tested for their antiplasmodial activity against a Plasmodium falciparum chloroquine resistant and sensitive strains (W2 and 3D7, respectively). Results: Thirty-one substances were efficiently obtained by the proposed routes with an overall yield of 25-53%. The active substances in the antiplasmodial test displayed IC50 values ranging from 0.68-2.89μM and 0.85-2.07 μM against W2 and 3D7 strains, respectively. Conclusion: This study demonstrated the great potential of isocoumarin or 3,4-dihydroisocoumarin derivatives because practically all the tested substances were active against Plasmodium falciparum.
Subject: Química farmacêutica
Plasmodium falciparum
Malára
Sintese
Triazóis
language: eng
metadata.dc.publisher.country: Brasil
Publisher: Universidade Federal de Minas Gerais
Publisher Initials: UFMG
metadata.dc.publisher.department: ICX - DEPARTAMENTO DE QUÍMICA
Rights: Acesso Restrito
metadata.dc.identifier.doi: http://dx.doi.org/10.2174/1573406416666200602161047
URI: http://hdl.handle.net/1843/72108
Issue Date: 2021
metadata.dc.url.externa: https://www.eurekaselect.com/article/107051
metadata.dc.relation.ispartof: Medicinal Chemistry
Appears in Collections:Artigo de Periódico

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