- 期刊Journal of natural products(J Nat Prod)
- 发表时间2026-09-25
- 作者Sawai K, Todoroki Y, Nakamukai S, Matsuzawa Y, Noguchi K, Kato T, Mori T, Rai A, Hirai MY, Tsugawa H
- 卷期页码V89(9) : 2474-2485
- DOI10.1021/acs.jnatprod.6c00565
- PMID42913377
摘要机译
甘草(Glycyrrhiza)是一种药用植物,广泛用于大约70%的日本传统Kampo配方中,并且已知会产生具有不同药理特性的各种专门代谢物。尽管已经报道了数百种代谢物,但甘草的整体化学多样性仍然特征不佳。
在这里,使用从完全13C标记的甘草和光甘草的叶片和根部获得的质谱数据,我们确定了碳数,然后结合基于MS/MS相似性的分子网络进行分子式和子结构预测。
在排除了同位素峰、加合物和源片段等多余离子后,我们提取了3060个具有指定碳数的独特代谢物特征。其中,子结构信息被分配给四个植物组织中的1015个特征(33%),揭示了组织特异性代谢组谱。此外,我们在乌拉拉和G.
Glabra和Glycine max,蚕豆科的另一个成员。使用核磁共振波谱对其中两种化合物进行了结构表征。我们进一步提出了一种生物合成路线,涉及1-吡啶和丙二酰糖苷底物之间的自发反应,并使用真实标准确认了共轭产物的形成。
展开英文摘要原文
Licorice (Glycyrrhiza) is a medicinal plant widely used in approximately 70% of traditional Japanese Kampo formulations and is known to produce a wide array of specialized metabolites with diverse pharmacological properties. Although hundreds of metabolites have been reported, the overall chemical diversity of Glycyrrhiza remains poorly characterized. Here, using mass spectrometry data obtained from fully 13C-labeled leaves and roots of Glycyrrhiza uralensis and Glycyrrhiza glabra, we determined the carbon number, followed by the molecular formula and substructure prediction in combination with MS/MS similarity-based molecular networking. After excluding redundant ions, including isotopic peaks, adducts, and in-source fragments, we extracted 3060 unique metabolite features with assigned carbon numbers. Among these, substructure information was assigned to 1015 features (33%) across the four plant tissues, revealing tissue-specific metabolome profiles. Furthermore, we discovered five previously unreported homopipecolic acid-conjugated flavonoids in the roots of G. uralensis and G. glabra and Glycine max, another member of the Fabaceae family. Two of these compounds were structurally characterized using nuclear magnetic resonance spectroscopy. We further proposed a biosynthetic route involving a spontaneous reaction between 1-piperideine and malonyl glycoside substrates and confirmed the formation of the conjugated product using authentic standards.
相关物质
本页由系统自动抓取 PubMed 元数据生成;标题与摘要版权归原作者与期刊所有;机译内容仅供参考,请以英文原文为准;收录不代表本站观点,亦不作为用药或医疗建议。