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Cytotoxic Metabolites from Calophyllum tacamahaca Willd.: Isolation and Detection through Feature-Based Molecular Networking
Isocaloteysmannic acid (1), a new chromanone, was isolated from the leaf extract of the medicinal species Calophyllum tacamahaca Willd. along with 13 known metabolites belonging to the families of biflavonoids (2), xanthones (3–5, 10), coumarins (6–8) and triterpenes (9, 11–14). The structure of the...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222348/ https://www.ncbi.nlm.nih.gov/pubmed/37233623 http://dx.doi.org/10.3390/metabo13050582 |
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author | Gerometta, Elise Herbette, Gaëtan Garayev, Elnur Marvilliers, Arnaud Naubron, Jean-Valère Di Giorgio, Carole Campos, Pierre-Eric Clerc, Patricia Ledoux, Allison Frederich, Michel Baghdikian, Béatrice Grondin, Isabelle Gauvin-Bialecki, Anne |
author_facet | Gerometta, Elise Herbette, Gaëtan Garayev, Elnur Marvilliers, Arnaud Naubron, Jean-Valère Di Giorgio, Carole Campos, Pierre-Eric Clerc, Patricia Ledoux, Allison Frederich, Michel Baghdikian, Béatrice Grondin, Isabelle Gauvin-Bialecki, Anne |
author_sort | Gerometta, Elise |
collection | PubMed |
description | Isocaloteysmannic acid (1), a new chromanone, was isolated from the leaf extract of the medicinal species Calophyllum tacamahaca Willd. along with 13 known metabolites belonging to the families of biflavonoids (2), xanthones (3–5, 10), coumarins (6–8) and triterpenes (9, 11–14). The structure of the new compound was characterized based on nuclear magnetic resonance (NMR), high-resolution electrospray mass spectrometry (HRESIMS), ultraviolet (UV) and infrared (IR) data. Its absolute configuration was assigned through electronic circular dichroism (ECD) measurements. Compound (1) showed a moderate cytotoxicity against HepG2 and HT29 cell lines, with IC(50) values of 19.65 and 25.68 µg/mL, respectively, according to the Red Dye method. Compounds 7, 8 and 10–13 exhibited a potent cytotoxic activity, with IC(50) values ranging from 2.44 to 15.38 µg/mL, against one or both cell lines. A feature-based molecular networking (FBMN) approach led to the detection of a large amount of xanthones in the leaves extract, and particularly analogues of the cytotoxic isolated xanthone pyranojacareubin (10). |
format | Online Article Text |
id | pubmed-10222348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102223482023-05-28 Cytotoxic Metabolites from Calophyllum tacamahaca Willd.: Isolation and Detection through Feature-Based Molecular Networking Gerometta, Elise Herbette, Gaëtan Garayev, Elnur Marvilliers, Arnaud Naubron, Jean-Valère Di Giorgio, Carole Campos, Pierre-Eric Clerc, Patricia Ledoux, Allison Frederich, Michel Baghdikian, Béatrice Grondin, Isabelle Gauvin-Bialecki, Anne Metabolites Article Isocaloteysmannic acid (1), a new chromanone, was isolated from the leaf extract of the medicinal species Calophyllum tacamahaca Willd. along with 13 known metabolites belonging to the families of biflavonoids (2), xanthones (3–5, 10), coumarins (6–8) and triterpenes (9, 11–14). The structure of the new compound was characterized based on nuclear magnetic resonance (NMR), high-resolution electrospray mass spectrometry (HRESIMS), ultraviolet (UV) and infrared (IR) data. Its absolute configuration was assigned through electronic circular dichroism (ECD) measurements. Compound (1) showed a moderate cytotoxicity against HepG2 and HT29 cell lines, with IC(50) values of 19.65 and 25.68 µg/mL, respectively, according to the Red Dye method. Compounds 7, 8 and 10–13 exhibited a potent cytotoxic activity, with IC(50) values ranging from 2.44 to 15.38 µg/mL, against one or both cell lines. A feature-based molecular networking (FBMN) approach led to the detection of a large amount of xanthones in the leaves extract, and particularly analogues of the cytotoxic isolated xanthone pyranojacareubin (10). MDPI 2023-04-23 /pmc/articles/PMC10222348/ /pubmed/37233623 http://dx.doi.org/10.3390/metabo13050582 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gerometta, Elise Herbette, Gaëtan Garayev, Elnur Marvilliers, Arnaud Naubron, Jean-Valère Di Giorgio, Carole Campos, Pierre-Eric Clerc, Patricia Ledoux, Allison Frederich, Michel Baghdikian, Béatrice Grondin, Isabelle Gauvin-Bialecki, Anne Cytotoxic Metabolites from Calophyllum tacamahaca Willd.: Isolation and Detection through Feature-Based Molecular Networking |
title | Cytotoxic Metabolites from Calophyllum tacamahaca Willd.: Isolation and Detection through Feature-Based Molecular Networking |
title_full | Cytotoxic Metabolites from Calophyllum tacamahaca Willd.: Isolation and Detection through Feature-Based Molecular Networking |
title_fullStr | Cytotoxic Metabolites from Calophyllum tacamahaca Willd.: Isolation and Detection through Feature-Based Molecular Networking |
title_full_unstemmed | Cytotoxic Metabolites from Calophyllum tacamahaca Willd.: Isolation and Detection through Feature-Based Molecular Networking |
title_short | Cytotoxic Metabolites from Calophyllum tacamahaca Willd.: Isolation and Detection through Feature-Based Molecular Networking |
title_sort | cytotoxic metabolites from calophyllum tacamahaca willd.: isolation and detection through feature-based molecular networking |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222348/ https://www.ncbi.nlm.nih.gov/pubmed/37233623 http://dx.doi.org/10.3390/metabo13050582 |
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