Natural Products and Derivatives as Potential Zika virus Inhibitors: A Comprehensive Review
Authors:
- Rosângela Santos PereiraRPRosângela Santos Pereira
- Françoise Camila Pereira SantosFSFrançoise Camila Pereira Santos
- Priscilla Rodrigues Valadares CampanaPCPriscilla Rodrigues Valadares Campana
- Vivian Vasconcelos CostaVCVivian Vasconcelos Costa
- Rodrigo Maia de PáduaRPRodrigo Maia de Pádua
- Daniele G. SouzaDSDaniele G. Souza
- Mauro Martins TeixeiraMTMauro Martins Teixeira
- Fernão Castro BragaFBFernão Castro Braga
Open Access
Abstract
Zika virus (ZIKV) is an arbovirus whose infection in humans can lead to severe outcomes. This article reviews studies reporting the anti-ZIKV activity of natural products (NPs) and derivatives published from 1997 to 2022, which were carried out with NPs obtained from plants (82.4%) or semisynthetic/synthetic derivatives, fungi (3.1%), bacteria (7.6%), animals (1.2%) and marine organisms (1.9%) along with miscellaneous compounds (3.8%). Classes of NPs reported to present anti-ZIKV activity include polyphenols, triterpenes, alkaloids, and steroids, among others. The highest values of the selectivity index, the ratio between cytotoxicity and antiviral activity (SI = CC50/EC50), were reported for epigallocatechin gallate (SI ≥ 25,000) and anisomycin (SI ≥ 11,900) obtained from Streptomyces bacteria, dolastane (SI = 1246) isolated from the marine seaweed Canistrocarpus cervicorni, and the flavonol myricetin (SI ≥ 862). NPs mostly act at the stages of viral adsorption and internalization in addition to presenting virucidal effect. The data demonstrate the potential of NPs for developing new anti-ZIKV agents and highlight the lack of studies addressing their molecular mechanisms of action and pre-clinical studies of efficacy and safety in animal models. To the best of our knowledge, none of the active compounds has been submitted to clinical studies.Keywords
Funding Information
- Conselho Nacional de Desenvolvimento Científico e Tecnológico (421563/2018-4, 465425/2014-3)
- INCT-CNPq Program (421563/2018-4, 465425/2014-3)
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