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
{"title":"澳大利亚海绵Agelas axifera中ageline生物碱的驱虫潜能。","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","doi":"10.3390/md23070276","DOIUrl":null,"url":null,"abstract":"<p><p>A recent high-throughput screening of the NatureBank marine extract library (7616 samples) identified an extract from the Australian marine sponge <i>Agelas axifera</i> with in vitro activity against an economically important parasitic nematode, <i>Haemonchus contortus</i> (barber's pole worm). The bioassay-guided fractionation of the CH<sub>2</sub>Cl<sub>2</sub>/MeOH extract from <i>A. axifera</i> led to the purification of a new diterpene alkaloid, agelasine Z (<b>1</b>), together with two known compounds agelasine B (<b>2</b>) and oxoagelasine B (<b>3</b>). Brominated compounds (-)-mukanadin C (<b>4</b>) and 4-bromopyrrole-2-carboxylic acid (<b>5</b>) were also isolated from neighbouring UV-active fractions. All compounds, together with agelasine D (<b>6</b>) from NatureBank's pure compound library, were tested for in vitro anthelmintic activity against exsheathed third-stage (xL3s) and fourth-stage larvae (L4s) of <i>H. contortus</i> and young adult <i>Caenorhabditis elegans</i>. Compounds <b>1</b>, <b>2</b> and <b>6</b> induced an abnormal \"skinny\" phenotype, while compounds <b>2</b> and <b>6</b> also reduced the motility of <i>H. contortus</i> L4s by 50.5% and 51.8% at 100 µM, respectively. The minimal activity of agelasines against <i>C. elegans</i> 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-<i>d</i><sub>4</sub> at room temperature.</p>","PeriodicalId":18222,"journal":{"name":"Marine Drugs","volume":"23 7","pages":""},"PeriodicalIF":4.9000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Anthelmintic Potential of Agelasine Alkaloids from the Australian Marine Sponge <i>Agelas axifera</i>.\",\"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\",\"doi\":\"10.3390/md23070276\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A recent high-throughput screening of the NatureBank marine extract library (7616 samples) identified an extract from the Australian marine sponge <i>Agelas axifera</i> with in vitro activity against an economically important parasitic nematode, <i>Haemonchus contortus</i> (barber's pole worm). The bioassay-guided fractionation of the CH<sub>2</sub>Cl<sub>2</sub>/MeOH extract from <i>A. axifera</i> led to the purification of a new diterpene alkaloid, agelasine Z (<b>1</b>), together with two known compounds agelasine B (<b>2</b>) and oxoagelasine B (<b>3</b>). Brominated compounds (-)-mukanadin C (<b>4</b>) and 4-bromopyrrole-2-carboxylic acid (<b>5</b>) were also isolated from neighbouring UV-active fractions. All compounds, together with agelasine D (<b>6</b>) from NatureBank's pure compound library, were tested for in vitro anthelmintic activity against exsheathed third-stage (xL3s) and fourth-stage larvae (L4s) of <i>H. contortus</i> and young adult <i>Caenorhabditis elegans</i>. Compounds <b>1</b>, <b>2</b> and <b>6</b> induced an abnormal \\\"skinny\\\" phenotype, while compounds <b>2</b> and <b>6</b> also reduced the motility of <i>H. contortus</i> L4s by 50.5% and 51.8% at 100 µM, respectively. The minimal activity of agelasines against <i>C. elegans</i> 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-<i>d</i><sub>4</sub> at room temperature.</p>\",\"PeriodicalId\":18222,\"journal\":{\"name\":\"Marine Drugs\",\"volume\":\"23 7\",\"pages\":\"\"},\"PeriodicalIF\":4.9000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Marine Drugs\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3390/md23070276\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Marine Drugs","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3390/md23070276","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Anthelmintic Potential of Agelasine Alkaloids from the Australian Marine Sponge Agelas axifera.
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.
期刊介绍:
Marine Drugs (ISSN 1660-3397) publishes reviews, regular research papers and short notes on the research, development and production of drugs from the sea. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible, particularly synthetic procedures and characterization information for bioactive compounds. There is no restriction on the length of the experimental section.