Novel Discorhabdin Derivatives from Antarctic Sponges of the Genus Latrunculia: Expanding the Chemical Diversity of Polar Marine Natural Products

In this study, three Antarctic sponges of the genus <i>Latrunculia</i> were investigated, leading to the isolation of five unreported pyrroloiminoquinone alkaloids along with the known metabolite (+)-debromodiscorhabdin A (<b>3</b>). Three of the new metabolites were brominated, while the other two were found to have a C-5/C-8 sulfur bridge and a C-2/N-18 bridge. Three of the metabolites were shown to have a phenyl ketone substituent on C-14, not previously reported for discorhabdin derivatives. The cytotoxicity against the A549 cell lines was studied and compounds <b>1</b>-<b>4</b> showed activity of 4.3, 1.8, 1.0, and 23.9 µM, respectively, while no inhibition was found for <b>5</b> and <b>6</b>.

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Publication Details

Journal
Marine Drugs
Published
2025-10-15
DOI
https://doi.org/10.3390/md23100401
Citations
1
Primary Topic
Marine Sponges and Natural Products
Type
article
Field-Weighted Citation Impact
1.23
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article

Novel Discorhabdin Derivatives from Antarctic Sponges of the Genus Latrunculia: Expanding the Chemical Diversity of Polar Marine Natural Products

Sam Afoullouss, Bill J. Baker, Eduardo Rosa, Nerida G. Wilson et al.
1 citations
Marine Drugs
Marine Sponges and Natural Products
1.23
article

Novel Discorhabdin Derivatives from Antarctic Sponges of the Genus Latrunculia: Expanding the Chemical Diversity of Polar Marine Natural Products

Sam Afoullouss, Bill J. Baker, Eduardo Rosa, Nerida G. Wilson, Stine S. H. Olsen, Sydney K. Morrow, Kaley Geu
article en
1 citations

Abstract

In this study, three Antarctic sponges of the genus <i>Latrunculia</i> were investigated, leading to the isolation of five unreported pyrroloiminoquinone alkaloids along with the known metabolite (+)-debromodiscorhabdin A (<b>3</b>). Three of the new metabolites were brominated, while the other two were found to have a C-5/C-8 sulfur bridge and a C-2/N-18 bridge. Three of the metabolites were shown to have a phenyl ketone substituent on C-14, not previously reported for discorhabdin derivatives. The cytotoxicity against the A549 cell lines was studied and compounds <b>1</b>-<b>4</b> showed activity of 4.3, 1.8, 1.0, and 23.9 µM, respectively, while no inhibition was found for <b>5</b> and <b>6</b>.

Marine DrugsVol. 23(10)
Australian Museum (AU), The University of Western Australia (AU), University of South Florida (US), Western Australian Museum (AU)
Openalex Percentile: Top 17%
Marine Sponges and Natural Products
1.23
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