Macrocarpane-Type Sesquiterpenes from Laurencia microcladia

Seven undescribed sesquiterpenes featuring an uncommon macrocarpane skeleton, laurocarpanes A–G (1–7), were isolated from specimens of Laurencia microcladia collected in Fuerteventura, the Canary Islands. The identification of these macrocarpane-type metabolites is of particular interest from both chemical and chemotaxonomic perspectives, as it highlights distinctive biosynthetic capabilities within the studied species and further expands current knowledge regarding the distribution of this uncommon structural class in marine organisms. Their structures and configurational assignments were determined by a comprehensive NMR study, high-resolution mass spectrometry, and coupling constant evaluations. A biosynthetic model was proposed linking the assembly of the macrocarpane skeleton directly to an (S)-β-bisabolene monocyclic precursor, with the process mediated by vanadium-dependent bromoperoxidase (V-BPO). The plausibility of the proposed biogenetic formation of laurocarpanes A–G (1–7) was assessed through Density Functional Theory (DFT) calculations.

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Publication Details

Journal
Marine Drugs
Published
2026-09-09
DOI
https://doi.org/10.3390/md24090316
Primary Topic
Seaweed-derived Bioactive Compounds
Type
article
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article

Macrocarpane-Type Sesquiterpenes from Laurencia microcladia

Marı́a L. Souto, Manuel Norte, Jorge Juan Cabrera‐Trujillo, Antonio Hernández Daranas et al.
Marine Drugs
Seaweed-derived Bioactive Compounds
article

Macrocarpane-Type Sesquiterpenes from Laurencia microcladia

Marı́a L. Souto, Manuel Norte, Jorge Juan Cabrera‐Trujillo, Antonio Hernández Daranas, Adrián Gutiérrez-Cepeda, José J. Fernández
article en

Abstract

Seven undescribed sesquiterpenes featuring an uncommon macrocarpane skeleton, laurocarpanes A–G (1–7), were isolated from specimens of Laurencia microcladia collected in Fuerteventura, the Canary Islands. The identification of these macrocarpane-type metabolites is of particular interest from both chemical and chemotaxonomic perspectives, as it highlights distinctive biosynthetic capabilities within the studied species and further expands current knowledge regarding the distribution of this uncommon structural class in marine organisms. Their structures and configurational assignments were determined by a comprehensive NMR study, high-resolution mass spectrometry, and coupling constant evaluations. A biosynthetic model was proposed linking the assembly of the macrocarpane skeleton directly to an (S)-β-bisabolene monocyclic precursor, with the process mediated by vanadium-dependent bromoperoxidase (V-BPO). The plausibility of the proposed biogenetic formation of laurocarpanes A–G (1–7) was assessed through Density Functional Theory (DFT) calculations.

Marine DrugsVol. 24(9)
Consejo Superior de Investigaciones Científicas (ES), Universidad Autónoma de Santo Domingo (DO), Universidad de La Laguna (ES), Instituto de Productos Naturales y Agrobiología (ES)
Life below water
Openalex Percentile: Top 6%
Seaweed-derived Bioactive Compounds
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Macrocarpane-Type Sesquiterpenes from Laurencia microcladia — Marı́a L. Souto, Manuel Norte, et al. · Marine Drugs (2026) | TGRS Research Map | TGRS