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基于(+)-桉叶环氧醚,通过内生菌发酵对(+)-桉叶环氧醚类似物进行研究获得先导化合物,合成了强效的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)3C样蛋白酶抑制剂(+)-桉叶环氧醚-3,6-二酮(IC:0.048 μM)。

Potent SARS-CoV-2 3C-like protease inhibitor ( +)-eupenoxide-3,6-diketone (IC: 0.048 μM) was synthesized based on ( +)-eupenoxide; lead from ( +)-eupenoxide analogs study by endophytic fermentation.

作者信息

Maehara Shoji, Kumamoto Moeka, Nakajima Shogo, Hieda Yuhzo, Watashi Koichi, Hata Toshiyuki

机构信息

Faculty of Pharmacy and Pharmaceutical Sciences, Fukuyama University, Sanzo, 1 Gakuen-cho, Fukuyama, Hiroshima, 729-0292, Japan.

Department of Virology II, National Institute of Infectious Diseases, Toyama 1-23-1, Shinjuku-ku, Tokyo, 162-8640, Japan.

出版信息

J Nat Med. 2025 Mar;79(2):357-370. doi: 10.1007/s11418-024-01874-3. Epub 2025 Feb 3.

DOI:10.1007/s11418-024-01874-3
PMID:39899217
Abstract

Since the coronavirus disease 2019 (COVID-19) outbreak, research has been conducted on treatment and countermeasures against the causative severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). However, the development of new seeds is urgently needed because viruses have the characteristic of becoming resistant through mutation. We hypothesize that endophytes produce antiviral substances to combat foreign viruses in host plants. According to this hypothesis, the seeds of therapeutic agents for infectious diseases could be obtained from endophytes by culture experiments. This report found that Aspergillus sp. endophyte isolated from Catharanthus roseus produced ( +)-eupenoxide and its 3-ketone form with anti-SARS-CoV-2 activity. In addition, ( +)-eupenoxide-3,6-diketon was discovered as a new compound with potent 3C-like protease inhibitory activity (IC: 0.048 μM) by synthesis based on ( +)-eupenoxide. This finding could be an important evidence that endophytic fungi symbiosis with medicinal plants is useful as antiviral producers.

摘要

自2019年冠状病毒病(COVID-19)爆发以来,针对致病原严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的治疗和应对措施的研究一直在进行。然而,由于病毒具有通过突变产生抗性的特性,迫切需要开发新的毒株。我们假设内生菌会产生抗病毒物质以对抗宿主植物中的外来病毒。根据这一假设,通过培养实验可以从内生菌中获得传染病治疗剂的种子。本报告发现,从长春花中分离出的曲霉属内生菌产生了具有抗SARS-CoV-2活性的(+)-优潘氧化物及其3-酮形式。此外,基于(+)-优潘氧化物通过合成发现了(+)-优潘氧化物-3,6-二酮,这是一种具有强效3C样蛋白酶抑制活性(IC:0.048 μM)的新化合物。这一发现可能是一个重要证据,表明与药用植物共生的内生真菌作为抗病毒生产者是有用的。

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Potent SARS-CoV-2 3C-like protease inhibitor ( +)-eupenoxide-3,6-diketone (IC: 0.048 μM) was synthesized based on ( +)-eupenoxide; lead from ( +)-eupenoxide analogs study by endophytic fermentation.基于(+)-桉叶环氧醚,通过内生菌发酵对(+)-桉叶环氧醚类似物进行研究获得先导化合物,合成了强效的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)3C样蛋白酶抑制剂(+)-桉叶环氧醚-3,6-二酮(IC:0.048 μM)。
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本文引用的文献

1
Artificial intelligence-driven rational design of ionizable lipids for mRNA delivery.用于mRNA递送的可电离脂质的人工智能驱动的合理设计。
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CREST-A program for the exploration of low-energy molecular chemical space.
CREST——一个用于探索低能量分子化学空间的程序。
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4
Environmental differences between Japan and Indonesia provide endophyte diversity associated with Artemisia plant and variety of artemisinin derivatives in microbial conversion.日本和印度尼西亚的环境差异为内生菌多样性提供了条件,这些内生菌与青蒿植物有关,并且可以在微生物转化中产生各种青蒿素衍生物。
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Discovery and Crystallographic Studies of Trisubstituted Piperazine Derivatives as Non-Covalent SARS-CoV-2 Main Protease Inhibitors with High Target Specificity and Low Toxicity.三取代哌嗪衍生物作为非共价 SARS-CoV-2 主蛋白酶抑制剂的发现和晶体学研究:高靶标特异性和低毒性。
J Med Chem. 2022 Oct 13;65(19):13343-13364. doi: 10.1021/acs.jmedchem.2c01146. Epub 2022 Sep 15.
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Discovery of S-217622, a Noncovalent Oral SARS-CoV-2 3CL Protease Inhibitor Clinical Candidate for Treating COVID-19.S-217622 的发现:一种非共价的口服 SARS-CoV-2 3CL 蛋白酶抑制剂临床候选药物,用于治疗 COVID-19。
J Med Chem. 2022 May 12;65(9):6499-6512. doi: 10.1021/acs.jmedchem.2c00117. Epub 2022 Mar 30.
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