澳大利亚海绵Agelas axifera中ageline生物碱的驱虫潜能。

IF 4.9 2区 医学 Q1 CHEMISTRY, MEDICINAL
Marine Drugs Pub Date : 2025-07-01 DOI:10.3390/md23070276
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
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引用次数: 0

摘要

最近对NatureBank海洋提取物库(7616个样本)进行的高通量筛选发现,澳大利亚海绵Agelas axifera的提取物对一种具有重要经济意义的寄生虫——弯血线虫(Haemonchus tortus)具有体外活性。用生物测定法对茜草CH2Cl2/MeOH提取物进行分离,得到了一种新的二萜生物碱agelasine Z(1),以及两种已知的化合物agelasine B(2)和oxoagelasine B(3)。从邻近的uv活性馏分中还分离到溴化化合物(-)-mukanadin C(4)和4-溴吡咯-2-羧酸(5)。所有化合物与NatureBank纯化合物文库中的agelasine D(6)一起,对H. contortus和年轻成年秀丽隐杆线虫(Caenorhabditis elegans)的第三期(xL3s)和第四期幼虫(L4s)进行了体外驱虫活性测试。化合物1、2和6诱导了异常的“瘦”表型,而化合物2和6也使H. contortus L4s在100µM下的运动能力分别降低了50.5%和51.8%。agelasine对秀丽隐杆线虫年轻成虫的最低活性表明可能存在一种物种特异性机制,值得进一步研究。首次利用动力学研究探索了agelasine H-8'的意外稳定性,揭示了MeOH-d4在室温下的快速氘交换。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.

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来源期刊
Marine Drugs
Marine Drugs 医学-医药化学
CiteScore
9.60
自引率
14.80%
发文量
671
审稿时长
1 months
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.
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