Exploring the anti-Chagas activity of Zanthoxylum chiloperone’s seedlings through metabolomics and protein-ligand docking
Share
Metadata
Show full item recordAuthor(s)
Vera de Bilbao, Ninfa; Giebelhaus, Ryland T.; Dias, Ryan P.; Ferreira de Paredes, María Elena





Date of publishing
2025-03-18Type of publication
research articleSubject(s)
Abstract
This publication reports the controlled cultivation of Zanthoxylum chiloperone var. angustifolium Engl. (Rutaceae) in several growth substrates under controlled greenhouse conditions. This plant is well-known for its anti-Chagas (trypanocidal) activity, related to the presence of several β-carboline alkaloids. The metabolomic study of Z. chiloperone seedlings over two years of growth (2018–2020) was performed using comprehensive two-dimensional gas chromatography time-of-flight mass spectrometry (GC × GC-TOFMS). The canthin-6-one alkaloids, canthin-6-one and 5-methoxy-canthin-6-one, were putatively identified in Z. chiloperone extracts. Finally, in vitro and in silico studies of trypanocidal activity were performed, suggesting that canthin-6-one alkaloids could interact with the main pharmacological targets against Trypanosoma cruzi, cruzain protease, dihydroorotate dehydrogenase, lanosterol 14-alpha-demethylase, farnesyl diphosphate, and squalene synthases.