TY - JOUR
T1 - Identification of Secondary Metabolites from the Lichen Hypotrachyna enderythraea (Zahlbr.) Hale by HPLC-ESI-MS/MS
AU - Carrasco, Fernando
AU - Hernández, Wilfredo
AU - Castro, Nino
AU - Sivipaucar, Nelly
AU - Bongiorno, Bruno
AU - Chupayo, Oscar
AU - Raposo, Cesar
AU - Silva, Lúcia A.
AU - Rodilla, Jesus M.
AU - Carrasco, Eduardo
AU - Dávalos, Juan Z.
N1 - Publisher Copyright:
© 2026 by the authors.
PY - 2026/3
Y1 - 2026/3
N2 - In this study, sixteen secondary metabolites, including two chromones, four dibenzofurans, three lipids, three depsides, two aromatic compounds, a quinone, and a terpene, were detected in the methanol:acetone (1:1 v/v) extract of the lichen Hypotrachyna enderythraea (Zahlbr.) Hale, using High-Performance Liquid Chromatography coupled to Orbitrap Electrospray Ionization tandem Mass Spectrometry (HPLC-Orbitrap ESI tandem MS/MS). These metabolites were characterized by analysis of their exact molecular masses and corresponding fragmentation patterns. The retention times of the identified metabolites were compared with those of standard compounds, confirming the presence of naturally occurring bioactive compounds. Density Functional Theory (DFT) calculations were employed to investigate preferential deprotonation sites in representative polyprotic metabolites. All these findings may contribute to expanding the spectrum of compounds identified within the genus Hypotrachyna and to evaluating their potential biological activities.
AB - In this study, sixteen secondary metabolites, including two chromones, four dibenzofurans, three lipids, three depsides, two aromatic compounds, a quinone, and a terpene, were detected in the methanol:acetone (1:1 v/v) extract of the lichen Hypotrachyna enderythraea (Zahlbr.) Hale, using High-Performance Liquid Chromatography coupled to Orbitrap Electrospray Ionization tandem Mass Spectrometry (HPLC-Orbitrap ESI tandem MS/MS). These metabolites were characterized by analysis of their exact molecular masses and corresponding fragmentation patterns. The retention times of the identified metabolites were compared with those of standard compounds, confirming the presence of naturally occurring bioactive compounds. Density Functional Theory (DFT) calculations were employed to investigate preferential deprotonation sites in representative polyprotic metabolites. All these findings may contribute to expanding the spectrum of compounds identified within the genus Hypotrachyna and to evaluating their potential biological activities.
KW - Hypotrachyna species
KW - lichen
KW - secondary metabolite profiling
KW - UHPLC-MS-MS
UR - https://www.scopus.com/pages/publications/105034152622
U2 - 10.3390/molecules31060954
DO - 10.3390/molecules31060954
M3 - Artículo (Contribución a Revista)
C2 - 41900053
AN - SCOPUS:105034152622
SN - 1420-3049
VL - 31
JO - Molecules
JF - Molecules
IS - 6
M1 - 954
ER -