{"title":"从Diorygma sp.培养的地衣真菌中分离出一种新的瓜蓝烷倍半萜。","authors":"Nguyen-Hong-Nhi Phan, Thuc-Huy Duong, Huy Truong Nguyen, Thi-Hoai-Thu Nguyen, Ngoc-Hong Nguyen, Thi-Phi-Giao Vo, Thi-Minh-Dinh Tran, Jirapast Sichaem","doi":"10.1007/s10600-025-04633-2","DOIUrl":null,"url":null,"abstract":"<p>The cultured mycobiont of the Vietnamese crustose lichen <i>Diorygma</i> sp. was subjected to chemical investigation, which led to the isolation and characterization of a new guaiane sesquiterpene, diorygmone F (<b>1</b>), along with three known compounds, pruinosone, <i>β</i>-sitosterol, and methyl 4-hydroxybenzoate. Structural elucidation was achieved through extensive spectroscopic methods, including NMR, HR-ESI-MS, and ECD. Compound <b>1</b> displayed modest inhibitory activity against <i>α</i>-glucosidase, with an IC<sub>50</sub> value of 131 ± 1.4 μM, and showed no cytotoxicity against the HepG2 cancer cell line.</p>","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"61 2","pages":"297 - 299"},"PeriodicalIF":0.8000,"publicationDate":"2025-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A New Guaiane Sesquiterpene from the Cultured Lichen Mycobiont of Diorygma sp.\",\"authors\":\"Nguyen-Hong-Nhi Phan, Thuc-Huy Duong, Huy Truong Nguyen, Thi-Hoai-Thu Nguyen, Ngoc-Hong Nguyen, Thi-Phi-Giao Vo, Thi-Minh-Dinh Tran, Jirapast Sichaem\",\"doi\":\"10.1007/s10600-025-04633-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The cultured mycobiont of the Vietnamese crustose lichen <i>Diorygma</i> sp. was subjected to chemical investigation, which led to the isolation and characterization of a new guaiane sesquiterpene, diorygmone F (<b>1</b>), along with three known compounds, pruinosone, <i>β</i>-sitosterol, and methyl 4-hydroxybenzoate. Structural elucidation was achieved through extensive spectroscopic methods, including NMR, HR-ESI-MS, and ECD. Compound <b>1</b> displayed modest inhibitory activity against <i>α</i>-glucosidase, with an IC<sub>50</sub> value of 131 ± 1.4 μM, and showed no cytotoxicity against the HepG2 cancer cell line.</p>\",\"PeriodicalId\":514,\"journal\":{\"name\":\"Chemistry of Natural Compounds\",\"volume\":\"61 2\",\"pages\":\"297 - 299\"},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2025-03-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry of Natural Compounds\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10600-025-04633-2\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry of Natural Compounds","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10600-025-04633-2","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
A New Guaiane Sesquiterpene from the Cultured Lichen Mycobiont of Diorygma sp.
The cultured mycobiont of the Vietnamese crustose lichen Diorygma sp. was subjected to chemical investigation, which led to the isolation and characterization of a new guaiane sesquiterpene, diorygmone F (1), along with three known compounds, pruinosone, β-sitosterol, and methyl 4-hydroxybenzoate. Structural elucidation was achieved through extensive spectroscopic methods, including NMR, HR-ESI-MS, and ECD. Compound 1 displayed modest inhibitory activity against α-glucosidase, with an IC50 value of 131 ± 1.4 μM, and showed no cytotoxicity against the HepG2 cancer cell line.
期刊介绍:
Chemistry of Natural Compounds publishes reviews and general articles about the structure of different classes of natural compounds, the chemical characteristics of botanical families, genus, and species, to establish the comparative laws and connection between physiological activity and the structure of substances.