Chemical constituents of Crepis napifera (Franch.) Babc. and their anti-inflammatory activities.

IF 1.9 3区 化学 Q3 CHEMISTRY, APPLIED
Gen-Lin Yang, Zhi-Nan Mei
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引用次数: 0

Abstract

A chemical study of Crepis napifera led to the isolation and identification of four compounds. Spectroscopic analysis revealed that these compounds belong to the class of eudesmane sesquiterpenes;guaiacane sesquiterpenes and their derivatives, including two novel compounds named Huanyangshen A (1) and Huanyangshen B (2). The absolute configurations of these new compounds were established through the comparison of experimental and calculated ECD spectra. Additionally, the anti-inflammatory properties of these compounds were assessed by evaluating their ability to inhibit LPS-induced NO production in RAW264.7 cells. The results indicated that the compound had potential inhibitory activity. Among them, the IC50 value of compound 1 was 24.97 μM, which was comparable to the IC50 value of the positive control minocycline (31.54 μM).

麻豆的化学成分(法国)Babc。以及它们的抗炎作用。
通过对该植物的化学研究,分离鉴定了4个化合物。光谱分析结果表明,这些化合物分别属于桂烷倍半萜类、愈创木烷倍半萜类及其衍生物,其中有两个新化合物命名为欢羊参A(1)和欢羊参B(2)。通过比较实验和计算的ECD谱,确定了这些新化合物的绝对构型。此外,通过评估这些化合物抑制lps诱导的RAW264.7细胞NO生成的能力来评估它们的抗炎特性。结果表明,该化合物具有潜在的抑制活性。其中,化合物1的IC50值为24.97 μM,与阳性对照米诺环素的IC50值(31.54 μM)相当。
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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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