# Anthelmintic Potential of Agelasine Alkaloids from the Australian Marine Sponge Agelas axifera

**Authors:** Kanchana Wijesekera, Aya C. Taki, Joseph J. Byrne, Darren C. Holland, Ian D. Jenkins, Merrick G. Ekins, Anthony R. Carroll, Robin B. Gasser, Rohan A. Davis

PMC · DOI: 10.3390/md23070276 · 2025-07-01

## TL;DR

Scientists found that compounds from a marine sponge in Australia can kill parasitic worms in lab tests, suggesting potential new treatments.

## Contribution

The study identifies new anthelmintic compounds from Agelas axifera and explores their effects on parasitic nematodes.

## Key findings

- Agelasine compounds induced a 'skinny' phenotype in nematode larvae.
- Agelasines reduced motility in Haemonchus contortus larvae by over 50%.
- Agelasine H-8′ was found to be chemically unstable under certain conditions.

## Abstract

A recent high-throughput screening of the NatureBank marine extract library (7616 samples) identified an extract from the Australian marine sponge Agelas axifera with in vitro activity against an economically important parasitic nematode, Haemonchus contortus (barber’s pole worm). The bioassay-guided fractionation of the CH2Cl2/MeOH extract from A. axifera led to the purification of a new diterpene alkaloid, agelasine Z (1), together with two known compounds agelasine B (2) and oxoagelasine B (3). Brominated compounds (–)-mukanadin C (4) and 4-bromopyrrole-2-carboxylic acid (5) were also isolated from neighbouring UV-active fractions. All compounds, together with agelasine D (6) from NatureBank’s pure compound library, were tested for in vitro anthelmintic activity against exsheathed third-stage (xL3s) and fourth-stage larvae (L4s) of H. contortus and young adult Caenorhabditis elegans. Compounds 1, 2 and 6 induced an abnormal “skinny” phenotype, while compounds 2 and 6 also reduced the motility of H. contortus L4s by 50.5% and 51.8% at 100 µM, respectively. The minimal activity of agelasines against C. elegans young adults suggests a possible species-specific mechanism warranting further investigation. For the first time, the unexpected lability of agelasine H-8′ was explored using kinetic studies, revealing rapid deuterium exchange in MeOH-d4 at room temperature.

## Linked entities

- **Chemicals:** agelasine B (PubChem CID 10049789), (–)-mukanadin C (PubChem CID 10704662), 4-bromopyrrole-2-carboxylic acid (PubChem CID 2741381), agelasine D (PubChem CID 11775481)
- **Species:** Agelas axifera (taxon 332232), Haemonchus contortus (taxon 6289), Caenorhabditis elegans (taxon 6239)

## Full-text entities

- **Chemicals:** agelasine D (MESH:C509934), Alkaloids (MESH:D000470), agelasine B (MESH:C054174), deuterium (MESH:D003903), (-)-mukanadin C (MESH:C000608457), CH2Cl2 (MESH:D008752), diterpene alkaloid (MESH:D000077743), 4-bromopyrrole-2-carboxylic acid (-)
- **Species:** Agelas axifera (species) [taxon 332232], C. elegans [taxon 328850], Haemonchus contortus (barber pole worm, species) [taxon 6289], Caenorhabditis elegans (species) [taxon 6239]

## Figures

13 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12299395/full.md

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Source: https://tomesphere.com/paper/PMC12299395