[:pb]N-(2-(arylmethylimino)ethyl)-7-chloroquinolin-4-amine derivatives, synthesized by thermal and ultrasonic means, are endowed with anti-Zika virus activity[:]

[:pb]Authors: Barbosa-Lima, G. ; Pinto, L. S.; Kaiser, C. R.; Wardell, J. L.; De Freitas, C. S.; Vieira, Y. R ; Marttorelli, A.; Neto, J. C.; Bozza, P. T.; Wardell, S. M. S. V.; De Souza, M. V. N.; Souza, T. M. L.
Source: European Journal of Medicinal Chemistry, v. 127, p. 434-441, 2017
Publisher:Science Direct

Abstract

Zika virus (ZIKV), an emerging Flavivirus, was recently associated with severe neurological complications and congenital diseases. Therefore, development of antiviral agents capable of inhibiting ZIKV replication is urgent. Chloroquine is a molecule with a confirmed safety history for use with pregnant women, and has been found to exhibit anti-ZIKV activity at concentrations around 10 μM. This suggests that modifications to the chloroquine structure could be promising for obtaining more effective anti-ZIKV agents. Here, we report the ability of a series of N-(2-(arylmethylimino)ethyl)-7-chloroquinolin-4-amine derivatives to inhibit ZIKV replication in vitro. We have found that the quinoline derivative, N-(2-((5-nitrofuran-2-yl)methylimino)ethyl)-7-chloroquinolin-4-amine, 40, was the most potent compound within this series, reducing ZIKV replication by 72% at 10 μM. Compound 40 exhibits an EC₅₀ value of 0.8 ± 0.07 μM, compared to that of chloroquine of 12 ± 3.2 μM. Good activities were also obtained for other compounds, including those with aryl groups = phenyl, 4-fluorophenyl, 4-nitrophenyl, 2,6-dimethoxyphenyl, 3-pyridinyl and 5-nitrothien-2-yl. Syntheses of these quinoline derivatives have been obtained both by thermal and ultrasonic means. The ultrasonic method produced comparable yields to the thermal (reflux) method in very much shorter times 30–180 s compared to 30–180 min reactions times. These results indicate that this group of compounds is a good follow-up point for the potential discovery of new drugs against the Zika disease.

Keywords: zika virus, quinoline derivatives, sonochemical method

Document Type: Research Article

DOI: 10.1016/j.ejmech.2017.01.007

Publication date: 15 de fevereiro de 2017

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