Atabay Kokanov , Hequn Yang , Dan Tang , Artyk Kokanov , Jiangyu Zhao , Haji Akber Aisa
{"title":"大戟科植物中的 Tigliane 和 premyrsinane 二萜及其细胞毒性活性","authors":"Atabay Kokanov , Hequn Yang , Dan Tang , Artyk Kokanov , Jiangyu Zhao , Haji Akber Aisa","doi":"10.1016/j.fitote.2025.106525","DOIUrl":null,"url":null,"abstract":"<div><div>Five undescribed tigliane and premyrsinane diterpenoids, euphomonophane A-E (<strong>1</strong>–<strong>5</strong>), along with a known diterpenoid (<strong>6</strong>), were isolated from the whole plant of <em>Euphorbia monostyla</em>, and their chemical structures were elucidated based on extensive spectroscopic analysis, including HRESIMS, 1D and 2D NMR data. The absolute structures of new compounds <strong>1</strong>–<strong>5</strong> were rechecked by ECD calculation. These diterpenoids were evaluated for their cytotoxic activity on the cancer cell line Hela, MCF7, and HCT8 by MTT assay and compounds <strong>4</strong> (IC<sub>50</sub> 39.86 ± 2.65 μM) revealed moderate cytotoxic potential against Hela cells compared to Doxorubicin (DOX, IC<sub>50</sub> 0.80 ± 0.03 μM), while compounds <strong>1</strong>–<strong>6</strong> possessed no cytotoxicity against MCF7 and HCT8 cells.</div></div>","PeriodicalId":12147,"journal":{"name":"Fitoterapia","volume":"183 ","pages":"Article 106525"},"PeriodicalIF":2.5000,"publicationDate":"2025-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tigliane and premyrsinane diterpenoids from Euphorbia monostyla and their cytotoxic activity\",\"authors\":\"Atabay Kokanov , Hequn Yang , Dan Tang , Artyk Kokanov , Jiangyu Zhao , Haji Akber Aisa\",\"doi\":\"10.1016/j.fitote.2025.106525\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Five undescribed tigliane and premyrsinane diterpenoids, euphomonophane A-E (<strong>1</strong>–<strong>5</strong>), along with a known diterpenoid (<strong>6</strong>), were isolated from the whole plant of <em>Euphorbia monostyla</em>, and their chemical structures were elucidated based on extensive spectroscopic analysis, including HRESIMS, 1D and 2D NMR data. The absolute structures of new compounds <strong>1</strong>–<strong>5</strong> were rechecked by ECD calculation. These diterpenoids were evaluated for their cytotoxic activity on the cancer cell line Hela, MCF7, and HCT8 by MTT assay and compounds <strong>4</strong> (IC<sub>50</sub> 39.86 ± 2.65 μM) revealed moderate cytotoxic potential against Hela cells compared to Doxorubicin (DOX, IC<sub>50</sub> 0.80 ± 0.03 μM), while compounds <strong>1</strong>–<strong>6</strong> possessed no cytotoxicity against MCF7 and HCT8 cells.</div></div>\",\"PeriodicalId\":12147,\"journal\":{\"name\":\"Fitoterapia\",\"volume\":\"183 \",\"pages\":\"Article 106525\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2025-04-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fitoterapia\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0367326X25001509\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fitoterapia","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0367326X25001509","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Tigliane and premyrsinane diterpenoids from Euphorbia monostyla and their cytotoxic activity
Five undescribed tigliane and premyrsinane diterpenoids, euphomonophane A-E (1–5), along with a known diterpenoid (6), were isolated from the whole plant of Euphorbia monostyla, and their chemical structures were elucidated based on extensive spectroscopic analysis, including HRESIMS, 1D and 2D NMR data. The absolute structures of new compounds 1–5 were rechecked by ECD calculation. These diterpenoids were evaluated for their cytotoxic activity on the cancer cell line Hela, MCF7, and HCT8 by MTT assay and compounds 4 (IC50 39.86 ± 2.65 μM) revealed moderate cytotoxic potential against Hela cells compared to Doxorubicin (DOX, IC50 0.80 ± 0.03 μM), while compounds 1–6 possessed no cytotoxicity against MCF7 and HCT8 cells.
期刊介绍:
Fitoterapia is a Journal dedicated to medicinal plants and to bioactive natural products of plant origin. It publishes original contributions in seven major areas:
1. Characterization of active ingredients of medicinal plants
2. Development of standardization method for bioactive plant extracts and natural products
3. Identification of bioactivity in plant extracts
4. Identification of targets and mechanism of activity of plant extracts
5. Production and genomic characterization of medicinal plants biomass
6. Chemistry and biochemistry of bioactive natural products of plant origin
7. Critical reviews of the historical, clinical and legal status of medicinal plants, and accounts on topical issues.