New Cyclopeptide and γ-Butyrolactone Derivatives from an Endophytic Strain of <i>Cophinforma mamane</i>

From an endophytic strain of Cophinforma mamane isolated from the leaves of Bixa orellana, a previously undescribed γ-butyrolactone compound (<b>2</b>) and three new cyclopentapeptides (<b>3</b>-<b>5</b>) have been isolated from the same strain, along with the known (4<i>R)</i>-striatisporolide A (<b>1</b>). Their structures were elucidated through extensive spectral analysis and DP4+ calculations. The two γ-butyrolactone derivatives (<b>1</b>, <b>2</b>) exhibited moderate inhibitory activity against axenic Leishmania infantum amastigotes (IC<sub>50</sub> = 13.33 and 4.43 μM, respectively), while only compound <b>2</b> displayed cytotoxic activity on Jurkat cells (17% growth inhibition at 1 μg/mL) and weak antibacterial activity against Enterococcus faecalis (MIC = 64 μg/mL).

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Journal
ACS Omega
Published
2025-05-19
DOI
https://doi.org/10.1021/acsomega.5c01292
Primary Topic
Traditional and Medicinal Uses of Annonaceae
Type
article
Field-Weighted Citation Impact
0.00

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article

New Cyclopeptide and γ-Butyrolactone Derivatives from an Endophytic Strain of Cophinforma mamane

Marieke Vansteelandt, Mohamed Haddad, Denis Jacquemin, Sandra Bourgeade‐Delmas et al.
ACS Omega
Traditional and Medicinal Uses of Annonaceae
article

New Cyclopeptide and γ-Butyrolactone Derivatives from an Endophytic Strain of Cophinforma mamane

Marieke Vansteelandt, Mohamed Haddad, Denis Jacquemin, Sandra Bourgeade‐Delmas, Jean‐Luc Stigliani, Nicolás Fabre, Jérôme Graton, Carlos A. Amasifuén Guerra, Elise Crossay, Sergio Ortíz, Fatima Barakat, D. Titton, Clara Litot
article en

Abstract

From an endophytic strain of Cophinforma mamane isolated from the leaves of Bixa orellana, a previously undescribed γ-butyrolactone compound (<b>2</b>) and three new cyclopentapeptides (<b>3</b>-<b>5</b>) have been isolated from the same strain, along with the known (4<i>R)</i>-striatisporolide A (<b>1</b>). Their structures were elucidated through extensive spectral analysis and DP4+ calculations. The two γ-butyrolactone derivatives (<b>1</b>, <b>2</b>) exhibited moderate inhibitory activity against axenic Leishmania infantum amastigotes (IC<sub>50</sub> = 13.33 and 4.43 μM, respectively), while only compound <b>2</b> displayed cytotoxic activity on Jurkat cells (17% growth inhibition at 1 μg/mL) and weak antibacterial activity against Enterococcus faecalis (MIC = 64 μg/mL).

ACS OmegaVol. 10(21)
Centre National de la Recherche Scientifique (FR), Université Toulouse III - Paul Sabatier (FR), Lebanese University (LB), Université Fédérale de Toulouse Midi-Pyrénées (FR), Institut Universitaire de France (FR), National University Toribio Rodríguez de Mendoza (PE), Laboratoire de Chimie de Coordination (FR), Chimie et Interdisciplinarité, Synthèse, Analyse, Modélisation (FR), Institut de Recherche pour le Développement (FR), Université de Strasbourg (FR), Nantes Université (FR)
Institut de Recherche pour le Développement, Région Occitanie Pyrénées-Méditerranée
Openalex Percentile: Top 89%
Traditional and Medicinal Uses of Annonaceae
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