Two novel spermidine alkaloids from the roots of Capparis acutifolia.

IF 1.6 3区 化学 Q3 CHEMISTRY, APPLIED Natural Product Research Pub Date : 2025-02-11 DOI:10.1080/14786419.2025.2458672
Yu-Xiao Han, Shu-Qing Kuai, Hui-Long Sun, Hong-Gang Wang
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Abstract

Acutifoline A and Acutifoline B (C1 and C2, respectively) are two novel spermidine alkaloids obtained from Capparis acutifolia roots. The structures of the novel compounds were determined through extensive spectroscopic methods, such as 1D and 2D nuclear magnetic resonance spectroscopy and high resolution-electrospray ionization-mass spectroscopy (HR-ESI-MS). In addition, the anti-rheumatoid arthritis activities of the compounds were evaluated.

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荆芥根中两个新的亚精胺生物碱。
针叶碱A和针叶碱B (C1和C2)是从针叶根中分离得到的两种新型亚精胺类生物碱。通过一维和二维核磁共振波谱和高分辨率电喷雾电离质谱(HR-ESI-MS)等广泛的波谱方法确定了新化合物的结构。此外,还对化合物的抗类风湿关节炎活性进行了评价。
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来源期刊
Natural Product Research
Natural Product Research 化学-医药化学
CiteScore
5.10
自引率
9.10%
发文量
605
审稿时长
2.1 months
期刊介绍: The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds. The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal. Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section. All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.
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