Guziliayi Kuerban , Ablajan Turak , Nannan Xu , Dan Tang , Deng Zang , Xiayidan Abulimiti , Jiangyu Zhao , Haji Akber Aisa
{"title":"黄花蒿中重排芥子烷型倍半萜的发现。","authors":"Guziliayi Kuerban , Ablajan Turak , Nannan Xu , Dan Tang , Deng Zang , Xiayidan Abulimiti , Jiangyu Zhao , Haji Akber Aisa","doi":"10.1016/j.phytochem.2025.114627","DOIUrl":null,"url":null,"abstract":"<div><div>Six undescribed sesquiterpenes artetourneforin F–K (<strong>1</strong>–<strong>6</strong>), along with six known compounds (<strong>7</strong>–<strong>12</strong>), were isolated from <em>Artemisia tournefortiana</em>. Their structures were established by 1D and 2D NMR spectroscopic data, HRESIMS, ECD, and quantum chemical calculations. Artetourneforin F–K (<strong>1</strong>–<strong>6</strong>) represented a rare 4,5-<em>seco</em> undescribed skeleton in natural sesquiterpenes, and a plausible biosynthetic pathway was proposed. The X-ray crystal structures of compounds <strong>7</strong> and <strong>8</strong> were reported for the first time. Compound <strong>9</strong> showed extremely significant anti-inflammatory and cytotoxicity activity against HeLa cell lines with IC<sub>50</sub> values of 0.87 ± 0.05 μM and 4.02 ± 0.15 μM, respectively. In the anti-vitiligo activity test, compounds <strong>8</strong> and <strong>10</strong> demonstrated activity in promoting melanogenesis in B16F10 cells. Compound <strong>8</strong> exhibited significant cytotoxicity against the HT29 and MCF7 cell lines, with IC<sub>50</sub> values of 6.40 ± 0.41 and 10.18 ± 0.49 μM, respectively.</div></div>","PeriodicalId":20170,"journal":{"name":"Phytochemistry","volume":"240 ","pages":"Article 114627"},"PeriodicalIF":3.4000,"publicationDate":"2025-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Discovery of rearranged eudesmane-type sesquiterpenes from Artemisia tournefortiana\",\"authors\":\"Guziliayi Kuerban , Ablajan Turak , Nannan Xu , Dan Tang , Deng Zang , Xiayidan Abulimiti , Jiangyu Zhao , Haji Akber Aisa\",\"doi\":\"10.1016/j.phytochem.2025.114627\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Six undescribed sesquiterpenes artetourneforin F–K (<strong>1</strong>–<strong>6</strong>), along with six known compounds (<strong>7</strong>–<strong>12</strong>), were isolated from <em>Artemisia tournefortiana</em>. Their structures were established by 1D and 2D NMR spectroscopic data, HRESIMS, ECD, and quantum chemical calculations. Artetourneforin F–K (<strong>1</strong>–<strong>6</strong>) represented a rare 4,5-<em>seco</em> undescribed skeleton in natural sesquiterpenes, and a plausible biosynthetic pathway was proposed. The X-ray crystal structures of compounds <strong>7</strong> and <strong>8</strong> were reported for the first time. Compound <strong>9</strong> showed extremely significant anti-inflammatory and cytotoxicity activity against HeLa cell lines with IC<sub>50</sub> values of 0.87 ± 0.05 μM and 4.02 ± 0.15 μM, respectively. In the anti-vitiligo activity test, compounds <strong>8</strong> and <strong>10</strong> demonstrated activity in promoting melanogenesis in B16F10 cells. Compound <strong>8</strong> exhibited significant cytotoxicity against the HT29 and MCF7 cell lines, with IC<sub>50</sub> values of 6.40 ± 0.41 and 10.18 ± 0.49 μM, respectively.</div></div>\",\"PeriodicalId\":20170,\"journal\":{\"name\":\"Phytochemistry\",\"volume\":\"240 \",\"pages\":\"Article 114627\"},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2025-07-23\",\"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/S003194222500250X\",\"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/S003194222500250X","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}
Discovery of rearranged eudesmane-type sesquiterpenes from Artemisia tournefortiana
Six undescribed sesquiterpenes artetourneforin F–K (1–6), along with six known compounds (7–12), were isolated from Artemisia tournefortiana. Their structures were established by 1D and 2D NMR spectroscopic data, HRESIMS, ECD, and quantum chemical calculations. Artetourneforin F–K (1–6) represented a rare 4,5-seco undescribed skeleton in natural sesquiterpenes, and a plausible biosynthetic pathway was proposed. The X-ray crystal structures of compounds 7 and 8 were reported for the first time. Compound 9 showed extremely significant anti-inflammatory and cytotoxicity activity against HeLa cell lines with IC50 values of 0.87 ± 0.05 μM and 4.02 ± 0.15 μM, respectively. In the anti-vitiligo activity test, compounds 8 and 10 demonstrated activity in promoting melanogenesis in B16F10 cells. Compound 8 exhibited significant cytotoxicity against the HT29 and MCF7 cell lines, with IC50 values of 6.40 ± 0.41 and 10.18 ± 0.49 μM, respectively.
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.