Junchi Wang , Xiaoshuang Huo , Huaxiang Wang, Aijun Dong, Qi Zheng, Jianyong Si
{"title":"新疆阿魏空气部分未描述的倍半萜香豆素及其对脂多糖刺激的RAW 264.7巨噬细胞的抗炎活性","authors":"Junchi Wang , Xiaoshuang Huo , Huaxiang Wang, Aijun Dong, Qi Zheng, Jianyong Si","doi":"10.1016/j.phytochem.2023.113664","DOIUrl":null,"url":null,"abstract":"<div><p><span>Eight undescribed sesquiterpene<span> coumarins (</span></span><strong>1</strong>–<strong>8</strong>) and twenty known ones (<strong>9</strong>–<strong>28</strong>), were isolated from the aerial parts of <span><em>Ferula</em><em> sinkiangensis</em></span><span><span><span> K. M. Shen. Their structures were elucidated based on the comprehensive analysis of UV, IR, HRESIMS, 1D, and </span>2D NMR data. The </span>absolute configuration of </span><strong>1</strong> was determined by single crystal X-Ray diffraction, while the absolute configurations of <strong>2</strong>–<strong>8</strong><span> were determined by comparisons of experimental and calculated electrostatic circular dichroism spectra. Compound </span><strong>2</strong> is the first hydroperoxy sesquiterpene coumarin from the genus <em>Ferula</em>, while compound <strong>8</strong><span> has an unusual 5′,8′-peroxo bridge. Griess reaction results indicated compound </span><strong>18</strong><span> significantly decreased nitric oxide production of the lipopolysaccharide-stimulated RAW 264.7 macrophages with an IC</span><sub>50</sub><span> value of 2.3 μM, and ELISA results revealed that compound </span><strong>18</strong> effectively inhibited tumor necrosis factor-<em>α</em>, interleukin (IL)-1<em>β</em>, and IL-6 expressions.</p></div>","PeriodicalId":20170,"journal":{"name":"Phytochemistry","volume":null,"pages":null},"PeriodicalIF":3.2000,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Undescribed sesquiterpene coumarins from the aerial parts of Ferula sinkiangensis and their anti-inflammatory activities in lipopolysaccharide-stimulated RAW 264.7 macrophages\",\"authors\":\"Junchi Wang , Xiaoshuang Huo , Huaxiang Wang, Aijun Dong, Qi Zheng, Jianyong Si\",\"doi\":\"10.1016/j.phytochem.2023.113664\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span>Eight undescribed sesquiterpene<span> coumarins (</span></span><strong>1</strong>–<strong>8</strong>) and twenty known ones (<strong>9</strong>–<strong>28</strong>), were isolated from the aerial parts of <span><em>Ferula</em><em> sinkiangensis</em></span><span><span><span> K. M. Shen. Their structures were elucidated based on the comprehensive analysis of UV, IR, HRESIMS, 1D, and </span>2D NMR data. The </span>absolute configuration of </span><strong>1</strong> was determined by single crystal X-Ray diffraction, while the absolute configurations of <strong>2</strong>–<strong>8</strong><span> were determined by comparisons of experimental and calculated electrostatic circular dichroism spectra. Compound </span><strong>2</strong> is the first hydroperoxy sesquiterpene coumarin from the genus <em>Ferula</em>, while compound <strong>8</strong><span> has an unusual 5′,8′-peroxo bridge. Griess reaction results indicated compound </span><strong>18</strong><span> significantly decreased nitric oxide production of the lipopolysaccharide-stimulated RAW 264.7 macrophages with an IC</span><sub>50</sub><span> value of 2.3 μM, and ELISA results revealed that compound </span><strong>18</strong> effectively inhibited tumor necrosis factor-<em>α</em>, interleukin (IL)-1<em>β</em>, and IL-6 expressions.</p></div>\",\"PeriodicalId\":20170,\"journal\":{\"name\":\"Phytochemistry\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2023-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Phytochemistry\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0031942223000808\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0031942223000808","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Undescribed sesquiterpene coumarins from the aerial parts of Ferula sinkiangensis and their anti-inflammatory activities in lipopolysaccharide-stimulated RAW 264.7 macrophages
Eight undescribed sesquiterpene coumarins (1–8) and twenty known ones (9–28), were isolated from the aerial parts of Ferula sinkiangensis K. M. Shen. Their structures were elucidated based on the comprehensive analysis of UV, IR, HRESIMS, 1D, and 2D NMR data. The absolute configuration of 1 was determined by single crystal X-Ray diffraction, while the absolute configurations of 2–8 were determined by comparisons of experimental and calculated electrostatic circular dichroism spectra. Compound 2 is the first hydroperoxy sesquiterpene coumarin from the genus Ferula, while compound 8 has an unusual 5′,8′-peroxo bridge. Griess reaction results indicated compound 18 significantly decreased nitric oxide production of the lipopolysaccharide-stimulated RAW 264.7 macrophages with an IC50 value of 2.3 μM, and ELISA results revealed that compound 18 effectively inhibited tumor necrosis factor-α, interleukin (IL)-1β, and IL-6 expressions.
期刊介绍:
Phytochemistry is a leading international journal publishing studies of plant chemistry, biochemistry, molecular biology and genetics, structure and bioactivities of phytochemicals, including ''-omics'' and bioinformatics/computational biology approaches. Phytochemistry is a primary source for papers dealing with phytochemicals, especially reports concerning their biosynthesis, regulation, and biological properties both in planta and as bioactive principles. Articles are published online as soon as possible as Articles-in-Press and in 12 volumes per year. Occasional topic-focussed special issues are published composed of papers from invited authors.