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Anti-Zika Virus Activity and Isolation of Flavonoids from Ethanol Extracts of Curatella americana L. Leaves.
- Source :
-
Molecules (Basel, Switzerland) [Molecules] 2023 Mar 10; Vol. 28 (6). Date of Electronic Publication: 2023 Mar 10. - Publication Year :
- 2023
-
Abstract
- The ethnomedicinal plant Curatella americana L. (Dilleniaceae) is a common shrub in the Brazilian Cerrado, whose ethanolic extract showed significant in vitro anti-Zika virus activity by the MTT colorimetric method. Currently, there is no drug in clinical use specifically for the treatment of this virus; therefore, in this work, the antiviral and cytotoxic properties of the ethanolic extract, fractions, and compounds were evaluated. The ethanolic extract of the leaves showed no cytotoxicity for the human MRC-5 cell and was moderately cytotoxic for the Vero cell (CC <subscript>50</subscript> 161.5 ± 2.01 µg/mL). This extract inhibited the Zika virus multiplication cycle with an EC <subscript>50</subscript> of 85.2 ± 1.65 µg/mL. This extract was fractionated using the liquid-liquid partition technique, and the ethyl acetate fraction showed significant activity against the Zika virus with an EC <subscript>50</subscript> of 40.7 ± 2.33 µg/mL. From the ethyl acetate fraction, the flavonoids quercetin-3- O -hexosylgallate ( 1 ), quercetin-3- O -glucoside ( 2 ), and quercetin ( 5 ) were isolated, and in addition to these compounds, a mixture of quercetin-3- O -rhamnoside ( 3 ) and quercetin-3- O -arabinoside ( 4 ) was also obtained. The isolated compounds quercetin and quercetin-3-O-hexosylgallate inhibited the viral cytopathic effect at an EC <subscript>50</subscript> of 18.6 ± 2.8 and 152.8 ± 2.0, respectively. Additionally, analyses by liquid chromatography coupled to a mass spectrometer allowed the identification of another 24 minor phenolic constituents present in the ethanolic extract and in the ethyl acetate fraction of this species.
Details
- Language :
- English
- ISSN :
- 1420-3049
- Volume :
- 28
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Molecules (Basel, Switzerland)
- Publication Type :
- Academic Journal
- Accession number :
- 36985517
- Full Text :
- https://doi.org/10.3390/molecules28062546