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ACS omega · 2025

Bioactivities and Phytochemical Profiling of Trigynaea axilliflora from Brazil.

СтатьяНазвание и аннотация: Перевод в очереди
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Fonseca Natyele Rodrigues, Andrade Diogo Folly Gomes, Scaffo Julia Chaves, Rezende Bismarck, Macario de Simas Gonçalves Vitória, Bazilio Dos Santos Yure, Barros de Andrade Maria Eduarda, Calumbi Karine Simões, Longue Milena, de Araújo Penna Bruno, Lobão Adriana Quintella, Rocha Leandro Machado, Valverde Alessandra Leda, Montes Guilherme Carneiro, Rheder Fagundes Pascoal Aislan Cristina, Abreu Lucas Silva

Аннотация

Brazil is a country with the greatest biodiversity in the world, but much of it is still largely unexplored. Trigynaea axilliflora (Annonaceae) is a Brazilian plant species that has not been previously studied. This research aimed to characterize the chemical constituents and evaluate the biological activities of the extract, fractions and isolated compounds. Xylopine, a major compound isolated from this extract, is an aporphine alkaloid and a chemotaxonomic marker of this family, whose structure was confirmed by 1H/13C NMR and HRESIMS. HPLC-UV-ESI-qTOF dereplication indicated that xylopine and seven other aporphine alkaloids were present in the crude extract. A solvent washing procedure allowed the recovery of 138 mg of xylopine, with a yield of 13.8% (138 mg/g crude extract) and 95% purity by HPLC-DAD. Cytotoxicity by the MTT assay showed that xylopine was active against MG-63 osteosarcoma cells (IC50 = 5.5 μg/mL), with a selectivity index (SI = 0.63) indicating a favorable selectivity compared to doxorubicin (SI = 0.22). Antibacterial assays demonstrated the inhibition of Staphylococcus aureus and Escherichia coli by the ethanolic extract and chloroform fraction (MIC 125-500 μg/mL), as well as by xylopine (MIC 62.5 μg/mL for S. aureus and 31.2 μg/mL for E. coli). To evaluate antinociceptive activity, the formalin test was used, and both the ethanolic extract and xylopine significantly reduced nociceptive behavior during the inflammatory phase from 123.8 ± 13.7 s (100%) to 71.3 ± 10.2 s (57.5%) and 1.3 ± 0.4 s (1%), respectively, at doses of 30 mg/kg. In silico pharmacokinetic analysis using SwissADME predicted favorable drug-likeness and oral bioavailability for xylopine, supporting its potential as a drug candidate. This study presents the first report on the chemical profile and bioactivities of T. axilliflora, suggesting it as a possible natural source of xylopine. This finding highlights the importance of phytochemical and pharmacological research in understanding Brazil's understudied flora.