Gui-Min Xue , Jin-Feng Xue , Jiang-Jing Duan , Hui-Ying Yang , Yan-Jun Sun , Hui Chen , Yan-Le Zhi , Zhi-Qiang Zhang , Rao Li , Dong-Rong Zhu , Guo-Sheng Li
{"title":"水仙的倍半萜类化合物。和装备。通过抑制糖酵解途径具有抗炎活性","authors":"Gui-Min Xue , Jin-Feng Xue , Jiang-Jing Duan , Hui-Ying Yang , Yan-Jun Sun , Hui Chen , Yan-Le Zhi , Zhi-Qiang Zhang , Rao Li , Dong-Rong Zhu , Guo-Sheng Li","doi":"10.1016/j.phytochem.2025.114608","DOIUrl":null,"url":null,"abstract":"<div><div>Six previously undescribed sesquiterpenoids, named achisetaces A–F (<strong>1</strong>–<strong>6</strong>), involving a rare C<sub>6</sub>–<em>O</em>–C<sub>10</sub> bridged guaianolide-type sesquiterpenoid (<strong>1</strong>), along with nine known analogues (<strong>7</strong>–<strong>15</strong>), were obtained from the aerial parts of <em>Achillea setacea</em> Waldst. & Kit. The undescribed structures of <strong>1</strong>–<strong>6</strong> including their absolute configurations were determined through spectroscopic techniques (IR, UV, HRESIMS, 1D and 2D NMR), combined with DP4+ NMR analysis and quantum electronic circular dichroism (ECD) calculations. The inhibitory effects of compounds <strong>1</strong>–<strong>15</strong> on nitric oxide (NO) production were evaluated in LPS-induced RAW 264.7 cells. Compounds <strong>6</strong> and <strong>10</strong> exhibited significant anti-inflammatory activities with IC<sub>50</sub> values of 1.56 ± 0.32 and 6.89 ± 0.47 μM, respectively. Moreover, a mechanistic study revealed that compound <strong>6</strong> exerted the anti-inflammatory activity by regulating the glycolytic pathway <em>via</em> suppression of PFKFB3 activation.</div></div>","PeriodicalId":20170,"journal":{"name":"Phytochemistry","volume":"239 ","pages":"Article 114608"},"PeriodicalIF":3.4000,"publicationDate":"2025-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sesquiterpenoids from Achillea setacea Waldst. & Kit. with anti-inflammatory activity by inhibiting the glycolytic pathway\",\"authors\":\"Gui-Min Xue , Jin-Feng Xue , Jiang-Jing Duan , Hui-Ying Yang , Yan-Jun Sun , Hui Chen , Yan-Le Zhi , Zhi-Qiang Zhang , Rao Li , Dong-Rong Zhu , Guo-Sheng Li\",\"doi\":\"10.1016/j.phytochem.2025.114608\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Six previously undescribed sesquiterpenoids, named achisetaces A–F (<strong>1</strong>–<strong>6</strong>), involving a rare C<sub>6</sub>–<em>O</em>–C<sub>10</sub> bridged guaianolide-type sesquiterpenoid (<strong>1</strong>), along with nine known analogues (<strong>7</strong>–<strong>15</strong>), were obtained from the aerial parts of <em>Achillea setacea</em> Waldst. & Kit. The undescribed structures of <strong>1</strong>–<strong>6</strong> including their absolute configurations were determined through spectroscopic techniques (IR, UV, HRESIMS, 1D and 2D NMR), combined with DP4+ NMR analysis and quantum electronic circular dichroism (ECD) calculations. The inhibitory effects of compounds <strong>1</strong>–<strong>15</strong> on nitric oxide (NO) production were evaluated in LPS-induced RAW 264.7 cells. Compounds <strong>6</strong> and <strong>10</strong> exhibited significant anti-inflammatory activities with IC<sub>50</sub> values of 1.56 ± 0.32 and 6.89 ± 0.47 μM, respectively. Moreover, a mechanistic study revealed that compound <strong>6</strong> exerted the anti-inflammatory activity by regulating the glycolytic pathway <em>via</em> suppression of PFKFB3 activation.</div></div>\",\"PeriodicalId\":20170,\"journal\":{\"name\":\"Phytochemistry\",\"volume\":\"239 \",\"pages\":\"Article 114608\"},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2025-07-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Phytochemistry\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0031942225002316\",\"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/S0031942225002316","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}
Sesquiterpenoids from Achillea setacea Waldst. & Kit. with anti-inflammatory activity by inhibiting the glycolytic pathway
Six previously undescribed sesquiterpenoids, named achisetaces A–F (1–6), involving a rare C6–O–C10 bridged guaianolide-type sesquiterpenoid (1), along with nine known analogues (7–15), were obtained from the aerial parts of Achillea setacea Waldst. & Kit. The undescribed structures of 1–6 including their absolute configurations were determined through spectroscopic techniques (IR, UV, HRESIMS, 1D and 2D NMR), combined with DP4+ NMR analysis and quantum electronic circular dichroism (ECD) calculations. The inhibitory effects of compounds 1–15 on nitric oxide (NO) production were evaluated in LPS-induced RAW 264.7 cells. Compounds 6 and 10 exhibited significant anti-inflammatory activities with IC50 values of 1.56 ± 0.32 and 6.89 ± 0.47 μM, respectively. Moreover, a mechanistic study revealed that compound 6 exerted the anti-inflammatory activity by regulating the glycolytic pathway via suppression of PFKFB3 activation.
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.