Chemical and Enantioselective Analysis of the Leaf Essential Oil from Varronia crenata Ruiz & Pav. Growing in Ecuador

Essential oils from species of the genus <i>Varronia</i> (Boraginaceae) are recognized for their chemical diversity and biological potential; however, phytochemical information on <i>Varronia crenata</i> Ruiz & Pav. remains scarce, despite its wide distribution in the Andean region. The aim of this study was to provide the first chemical and enantioselective characterization of the essential oil obtained from the leaves of <i>V. crenata</i> growing in Ecuador. Qualitative and quantitative analyses were carried out by GC-MS and GC-FID, respectively, using two columns with stationary phases of contrasting polarity. Compounds were identified by matching linear retention indices and mass spectra to literature references and quantified by external calibration using relative response factors (RRFs) calculated for each compound based on its combustion enthalpy. The most abundant constituents (≥3.0% on average between the two columns) of the essential oil of <i>V. crenata</i>, both in the nonpolar and polar stationary phases, were germacrene D (18.4%), <i>(E)</i>-β-caryophyllene (13.3%), α-copaene (10.4%), tricyclene (9.3%), δ-cadinene (8.9%), and α-pinene (8.3%). The volatile fraction was dominated by sesquiterpenes (60.2%) and monoterpenes (22.1%), while other chemical families were present in minor proportions. The enantioselective analysis was performed on two different columns, coated with stationary phases based on β-cyclodextrins: 2,3-diacetyl-6-<i>tert</i>-butyl-dimethylsilyl-β-cyclodextrin and 2,3-diethyl-6-<i>tert</i>-butyl-dimethylsilyl-β-cyclodextrin. Nine chiral compounds were analyzed; among them, <i>(1R,5R)</i>-(+)-α-pinene, <i>(1R,5R)</i>-(+)-sabinene, and <i>(S)</i>-(+)-β-phellandrene were detected as enantiomerically pure, while the other metabolites presented scalemic mixtures. Overall, the high content of bioactive sesquiterpenes and the observed stereochemical complexity highlight the potential pharmaceutical and agricultural relevance of <i>V. crenata</i> essential oil, while also providing novel chemotaxonomic information for the genus.

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Journal
Molecules
Published
2026-02-03
DOI
https://doi.org/10.3390/molecules31030532
Primary Topic
Sesquiterpenes and Asteraceae Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Chemical and Enantioselective Analysis of the Leaf Essential Oil from Varronia crenata Ruiz & Pav. Growing in Ecuador

Yessenia E. Maldonado, Karem Cazares, Gianluca Gilardoni, Omar Malagón et al.
Molecules
Sesquiterpenes and Asteraceae Studies
article

Chemical and Enantioselective Analysis of the Leaf Essential Oil from Varronia crenata Ruiz & Pav. Growing in Ecuador

Yessenia E. Maldonado, Karem Cazares, Gianluca Gilardoni, Omar Malagón, Nixon Cumbicus
article en

Abstract

Essential oils from species of the genus <i>Varronia</i> (Boraginaceae) are recognized for their chemical diversity and biological potential; however, phytochemical information on <i>Varronia crenata</i> Ruiz & Pav. remains scarce, despite its wide distribution in the Andean region. The aim of this study was to provide the first chemical and enantioselective characterization of the essential oil obtained from the leaves of <i>V. crenata</i> growing in Ecuador. Qualitative and quantitative analyses were carried out by GC-MS and GC-FID, respectively, using two columns with stationary phases of contrasting polarity. Compounds were identified by matching linear retention indices and mass spectra to literature references and quantified by external calibration using relative response factors (RRFs) calculated for each compound based on its combustion enthalpy. The most abundant constituents (≥3.0% on average between the two columns) of the essential oil of <i>V. crenata</i>, both in the nonpolar and polar stationary phases, were germacrene D (18.4%), <i>(E)</i>-β-caryophyllene (13.3%), α-copaene (10.4%), tricyclene (9.3%), δ-cadinene (8.9%), and α-pinene (8.3%). The volatile fraction was dominated by sesquiterpenes (60.2%) and monoterpenes (22.1%), while other chemical families were present in minor proportions. The enantioselective analysis was performed on two different columns, coated with stationary phases based on β-cyclodextrins: 2,3-diacetyl-6-<i>tert</i>-butyl-dimethylsilyl-β-cyclodextrin and 2,3-diethyl-6-<i>tert</i>-butyl-dimethylsilyl-β-cyclodextrin. Nine chiral compounds were analyzed; among them, <i>(1R,5R)</i>-(+)-α-pinene, <i>(1R,5R)</i>-(+)-sabinene, and <i>(S)</i>-(+)-β-phellandrene were detected as enantiomerically pure, while the other metabolites presented scalemic mixtures. Overall, the high content of bioactive sesquiterpenes and the observed stereochemical complexity highlight the potential pharmaceutical and agricultural relevance of <i>V. crenata</i> essential oil, while also providing novel chemotaxonomic information for the genus.

MoleculesVol. 31(3)
Universidad Técnica Particular de Loja (EC), Universidad Estatal Amazónica (EC), Escuela Superior Politécnica del Chimborazo (EC)
Universidad Técnica Particular de Loja, Università degli Studi di Torino
Openalex Percentile: Top 69%
Sesquiterpenes and Asteraceae Studies
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