| Literature DB >> 28857500 |
Jorge Ramírez1,2, Gianluca Gilardoni1, Miriam Jácome1, José Montesinos1, Marinella Rodolfi3, Maria Lidia Guglielminetti3, Cecila Cagliero4, Carlo Bicchi4, Giovanni Vidari2.
Abstract
This study describes the GC-FID, GC/MS, GC-O, and enantioselective GC analysis of the essential oil hydrodistilled from leaves of Lepechinica mutica (Lamiaceae), collected in Ecuador. GC-FID and GC/MS analyses allowed the characterization and quantification of 79 components, representing 97.3% of the total sample. Sesquiterpene hydrocarbons (38.50%) and monoterpene hydrocarbons (30.59%) were found to be the most abundant volatiles, while oxygenated sesquiterpenes (16.20%) and oxygenated monoterpenes (2.10%) were the minor components. In order to better characterize the oil aroma, the most important odorants, from the sensorial point of view, were identified by Aroma Extract Dilution Analysis (AEDA) GC-O. They were α-Pinene, β-Phellandrene, and Dauca-5,8-diene, exhibiting the characteristic woody, herbaceus, and earthy odors, respectively. Enantioselective GC analysis of L. mutica essential oil revealed the presence of twelve couples and two enantiomerically pure chiral monoterpenoids. Their enantiomeric excesses were from a few percent units to 100%. Moreover, the essential oil exhibited moderate in vitro activity against five fungal strains, being especially effective against M. canis, which is a severe zoophilic dermatophyte causal agent of pet and human infections.Entities:
Keywords: zzm321990Lepechinia muticazzm321990; Antifungal activity; Ecuador; Enantiomeric analysis; Gas chromatography-olfactometry
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Year: 2017 PMID: 28857500 DOI: 10.1002/cbdv.201700292
Source DB: PubMed Journal: Chem Biodivers ISSN: 1612-1872 Impact factor: 2.408