A Flavonoid‐Rich Extract of <i>Scoparia dulcis</i> L. Exhibits Antiviral Activity against Herpes Virus Type 1

This study investigated the phytochemical profile, cytotoxicity, and anti-herpetic activity of the hydroethanolic extract from Scoparia dulcis L. aerial parts. Mass spectrometry revealed the presence of 15 compounds. The extract showed low cytotoxicity in Vero cells, maintaining over 80% viability at concentrations up to 250 µg/mL. In vitro antiviral assays demonstrated that the extract significantly inhibited HSV-1 infectivity and increased cell protection at 25, 50, and 100 µg/mL. These results support the traditional medicinal use of S. dulcis and suggest its potential as a natural antiviral agent. The presence of multiple active compounds may contribute to its efficacy through synergistic effects. Overall, the findings encourage further investigation of S. dulcis as a source of bioactive molecules with potential for the development of alternative therapies against herpes simplex virus type 1.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2026-01-01
DOI
https://doi.org/10.1002/cbdv.202502903
Primary Topic
Natural product bioactivities and synthesis
Type
article
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article

A Flavonoid‐Rich Extract of Scoparia dulcis L. Exhibits Antiviral Activity against Herpes Virus Type 1

Emerson Michell da Silva Siqueira, Edilane Rodrigues Dantas de Araújo, Hugo Alexandre Oliveira Rocha, Norberto Peporine Lopes et al.
Chemistry & Biodiversity
Natural product bioactivities and synthesis
article

A Flavonoid‐Rich Extract of Scoparia dulcis L. Exhibits Antiviral Activity against Herpes Virus Type 1

Emerson Michell da Silva Siqueira, Edilane Rodrigues Dantas de Araújo, Hugo Alexandre Oliveira Rocha, Norberto Peporine Lopes, Leandro De Santis Ferreira, Emanuella de Aragão Tavares, Jovelina Samara Ferreira Alves, Silvana Maria Zucolotto, Francisco Leandro Medeiros de Lucena Jales, Renato Dantas‐Medeiros
article en

Abstract

This study investigated the phytochemical profile, cytotoxicity, and anti-herpetic activity of the hydroethanolic extract from Scoparia dulcis L. aerial parts. Mass spectrometry revealed the presence of 15 compounds. The extract showed low cytotoxicity in Vero cells, maintaining over 80% viability at concentrations up to 250 µg/mL. In vitro antiviral assays demonstrated that the extract significantly inhibited HSV-1 infectivity and increased cell protection at 25, 50, and 100 µg/mL. These results support the traditional medicinal use of S. dulcis and suggest its potential as a natural antiviral agent. The presence of multiple active compounds may contribute to its efficacy through synergistic effects. Overall, the findings encourage further investigation of S. dulcis as a source of bioactive molecules with potential for the development of alternative therapies against herpes simplex virus type 1.

Chemistry & BiodiversityVol. 23(1)
Universidade de Ribeirão Preto (BR), Universidade de São Paulo (BR), Universidade Federal do Rio Grande do Norte (BR)
Openalex Percentile: Top 95%
Natural product bioactivities and synthesis
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