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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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).
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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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