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4-羟基-3-甲基-2(1)-喹诺酮,最初从一种植物中发现,由某属土壤细菌产生:优势互变异构体的确定及抗氧化活性

4-Hydroxy-3-methyl-2(1)-quinolone, originally discovered from a plant, produced by a soil bacterium of the genus sp.: determination of a preferred tautomer and antioxidant activity.

作者信息

Li Dandan, Oku Naoya, Shinozaki Yukiko, Kurokawa Yoichi, Igarashi Yasuhiro

机构信息

Biotechnology Research Center and Department of Biotechnology, Toyama Prefectural University, 5180 Kurokawa, Imizu, Toyama 939-0398, Japan.

National Institute of Technology, Toyama College, 13 Hongo-machi, Toyama City, Toyama 939-8630, Japan.

出版信息

Beilstein J Org Chem. 2020 Jun 26;16:1489-1494. doi: 10.3762/bjoc.16.124. eCollection 2020.

Abstract

4-Hydroxy-3-methyl-2(1)-quinolone (), a molecule known for a long time and recently discovered from a plant without providing sufficient evidence to support the structure, was isolated from a fermentation extract of sp. 3Y-MMP isolated from a soil by a Zn enrichment culture. Detailed spectroscopic analyses by MS and NMR, combined with C chemical shift comparison with literature values of the related compounds and a synthetic preparation of , allowed its first full NMR characterization and identification of 2-quinolone but not 2-quinolinol () as the preferred tautomer for this heterocyclic system. While the metal-chelating activity was negligible, compound at 10 μM, a concentration lower than that in liquid production cultures, quenched hydroxy radical-induced chemiluminescence emitted by luminol by 86%. Because some species are pathogenic to plants and animals, the above result suggests that is a potential antioxidant to counteract reactive oxygen species-based immune response in the host organisms.

摘要

4-羟基-3-甲基-2(1)-喹诺酮( ),一种早已为人所知但最近从一种植物中发现却未提供足够结构支持证据的分子,是从通过锌富集培养从土壤中分离得到的sp. 3Y-MMP的发酵提取物中分离出来的。通过质谱(MS)和核磁共振(NMR)进行的详细光谱分析,结合与相关化合物文献值的碳化学位移比较以及 的合成制备,首次实现了其完整的核磁共振表征,并确定2-喹诺酮而非2-喹啉醇( )是该杂环体系的优势互变异构体。虽然其金属螯合活性可忽略不计,但化合物在10 μM(低于液体生产培养中的浓度)时,可使鲁米诺发出的羟基自由基诱导化学发光猝灭86%。由于某些 物种对植物和动物具有致病性,上述结果表明 是一种潜在的抗氧化剂,可对抗宿主生物体中基于活性氧的免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d830/7323622/6bd0a57158f5/Beilstein_J_Org_Chem-16-1489-g002.jpg

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