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珊瑚礁中的入侵海葵作为含硫和含氮代谢产物及细胞毒性5,8-环氧甾体的来源。

The Invasive Anemone sp. of the Coral Reef as a Source of Sulfur- and Nitrogen-Containing Metabolites and Cytotoxic 5,8-Epidioxy Steroids.

作者信息

Ahmed Atallah F, Dai Chang-Feng, Kuo Yao-Haur, Sheu Jyh-Horng

机构信息

Department of Marine Resources, National Sun Yat-sen University, Kaohsiung 804, Taiwan.

Department of Pharmacognosy, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.

出版信息

Metabolites. 2023 Mar 7;13(3):392. doi: 10.3390/metabo13030392.

DOI:10.3390/metabo13030392
PMID:36984832
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10056678/
Abstract

The -genus anemones were examined for their proteinaceous poisons over 50 years ago. On the other hand, the current research focuses on isolating and describing the non-proteinaceous secondary metabolites from the invasive anemones, which help take advantage of their population outbreak as a new source of chemical candidates and potential drug leads. From an organic extract of sp., a 1,2,4-thiadiazole-based alkaloid, identified as 3,5-bis(3-pyridinyl)-1,2,4-thiadiazole (), was found to be a new natural alkaloid despite being previously synthesized. The full assignment of NMR data of compound , based on the analysis of 2D NMR correlations, is reported herein for the first time. The proposed biosynthetic precursor thionicotinamide () was also isolated for the first time from nature along with nicotinamide (), uridine (), hypoxanthine (), and four 5,8-epidioxysteroids (-). A major secondary metabolite (-)-betonicine () was isolated from sp. and found for the first time in marine invertebrates. The four 5,8-epidioxysteroids, among other metabolites, exhibited cytotoxicity (IC 3.5-9.0 μg/mL) toward five cancer cell lines.

摘要

50多年前就对海葵属的蛋白质毒素进行了研究。另一方面,目前的研究重点是从入侵海葵中分离和描述非蛋白质次生代谢产物,这有助于利用其种群爆发作为化学候选物和潜在药物先导的新来源。从海葵属的有机提取物中,发现一种基于1,2,4-噻二唑的生物碱,鉴定为3,5-双(3-吡啶基)-1,2,4-噻二唑(化合物),尽管此前已合成,但它是一种新的天然生物碱。本文首次基于二维核磁共振相关性分析报道了化合物的核磁共振数据的完整归属。拟议的生物合成前体硫代烟酰胺(化合物)也首次与烟酰胺(化合物)、尿苷(化合物)、次黄嘌呤(化合物)和四种5,8-环氧甾体(化合物)一起从自然界中分离出来。从海葵属中分离出一种主要的次生代谢产物(-)-甜菜碱(化合物),并首次在海洋无脊椎动物中发现。这四种5,8-环氧甾体以及其他代谢产物对五种癌细胞系表现出细胞毒性(IC为3.5-9.0μg/mL)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3f1/10056678/59ae075aadba/metabolites-13-00392-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3f1/10056678/635f83898c61/metabolites-13-00392-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3f1/10056678/f7cb84288818/metabolites-13-00392-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3f1/10056678/73800f7e0a46/metabolites-13-00392-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3f1/10056678/725a66d0f91d/metabolites-13-00392-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3f1/10056678/59ae075aadba/metabolites-13-00392-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3f1/10056678/635f83898c61/metabolites-13-00392-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3f1/10056678/f7cb84288818/metabolites-13-00392-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3f1/10056678/73800f7e0a46/metabolites-13-00392-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3f1/10056678/725a66d0f91d/metabolites-13-00392-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3f1/10056678/59ae075aadba/metabolites-13-00392-g004.jpg

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2
Sea anemone venom: Ecological interactions and bioactive potential.海葵毒液:生态相互作用和生物活性潜力。
Toxicon. 2022 Mar;208:31-46. doi: 10.1016/j.toxicon.2022.01.004. Epub 2022 Jan 19.
3
Interactions of Sea Anemone Toxins with Insect Sodium Channel-Insights from Electrophysiology and Molecular Docking Studies.海葵毒素与昆虫钠离子通道的相互作用:电生理学和分子对接研究的启示。
Molecules. 2021 Feb 28;26(5):1302. doi: 10.3390/molecules26051302.
4
The Isolation of New Pore-Forming Toxins from the Sea Anemone Provides Insights into the Mechanisms of Actinoporin Evolution.从海葵中分离新型孔形成毒素,深入了解肌动蛋白孔形成蛋白进化的机制。
Toxins (Basel). 2019 Jul 10;11(7):401. doi: 10.3390/toxins11070401.
5
Sea Anemone Toxins: A Structural Overview.海葵毒素:结构概述。
Mar Drugs. 2019 Jun 1;17(6):325. doi: 10.3390/md17060325.
6
Peroxy steroids derived from plant and fungi and their biological activities.植物和真菌来源的过氧甾醇及其生物活性。
Appl Microbiol Biotechnol. 2018 Sep;102(18):7657-7667. doi: 10.1007/s00253-018-9211-2. Epub 2018 Jul 10.
7
Prompt treatment with uridine triacetate improves survival and reduces toxicity due to fluorouracil and capecitabine overdose or dihydropyrimidine dehydrogenase deficiency.提示:使用尿苷三乙酸酯进行及时治疗可以提高生存机会,并降低因氟尿嘧啶和卡培他滨过量或二氢嘧啶脱氢酶缺乏导致的毒性。
Toxicol Appl Pharmacol. 2018 Aug 15;353:67-73. doi: 10.1016/j.taap.2018.06.012. Epub 2018 Jun 13.
8
Multigene Family of Pore-Forming Toxins from Sea Anemone .海葵中的多基因孔形成毒素家族。
Mar Drugs. 2018 May 24;16(6):183. doi: 10.3390/md16060183.
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Molecules. 2017 Nov 2;22(11):1881. doi: 10.3390/molecules22111881.
10
Bioactive Steroids from the Formosan Soft Coral Umbellulifera petasites.来自台湾软珊瑚Petasites umbellulifera的生物活性甾体。
Mar Drugs. 2016 Oct 11;14(10):180. doi: 10.3390/md14100180.