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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Chemistry & Biodiver...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Chemistry & Biodiversity
Article . 2021 . Peer-reviewed
License: Wiley Online Library User Agreement
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A Rare Dirhamnosyl Flavonoid and Other Radical‐Scavenging Metabolites from Cynophalla mollis (Kunth) J. Presl and Colicodendron scabridum (Kunt) Seem. (Capparaceae) of Ecuador

Authors: Vladimir Morocho; Leslye Paola Valarezo; David Andrés Tapia; Luis Cartuche; Nixon Cumbicus; Gianluca Gilardoni;

A Rare Dirhamnosyl Flavonoid and Other Radical‐Scavenging Metabolites from Cynophalla mollis (Kunth) J. Presl and Colicodendron scabridum (Kunt) Seem. (Capparaceae) of Ecuador

Abstract

AbstractThe phytochemistry of Cynophalla mollis (Kunth) J. Presl and Colicodendron scabridum (Kunth), both belonging to the family Capparaceae, were investigated in this study for the first time. Lupeol, betulin, lutein, stachydrine and quercetin‐3,4’‐di‐O‐rhamnoside were isolated from C. mollis, whereas C. scabridum afforded lupeol, lutein, stachydrine, β‐sitosterol, stigmasterol, betonicine and narcissoside. All these compounds were purified by preparative liquid chromatography, in both open column and instrumental (MPLC) separation systems. Preparative TLC was also applied. They were all identified by 1H‐ and 13C‐NMR experiments. The complete structure of the very rare flavonoid quercetin‐3,4’‐di‐O‐rhamnoside was fully elucidated through DEPT‐135, COSY, HMQC and HMBC experiments, together with UV/VIS and FT‐IR spectrophotometry. Complete NMR data for quercetin‐3,4’‐di‐O‐rhamnoside in deuterated methanol were presented here for the first time. All the extracts did not exert antioxidant activity at the maximum tested dose of 1 mg/mL. Three out of the nine isolated compounds exerted a good spectrum of antioxidant capacity, being narcissoside the most active against ABTS radicals, with SC50=12.43 μM. It was followed by lutein and quercetin‐3,4’‐di‐O‐rhamnoside, with 40.92 μM and 46.10 μM, respectively.

Related Organizations
Keywords

Flavonoids, Plant Leaves, Magnetic Resonance Spectroscopy, Plant Extracts, Molecular Conformation, Quercetin, Ecuador, Free Radical Scavengers, Capparaceae

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
10
Top 10%
Average
Top 10%
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