{"title":"从真菌曲霉中提取的具有除草活性的结构多样的聚酮。","authors":"Fei Liu, Shanshan Hong, Xiaoxia Gu, Qian Zhang, Qin Li, Weiguang Sun, Chunmei Chen, Yonghui Zhang, Hucheng Zhu","doi":"10.1016/j.phytochem.2025.114631","DOIUrl":null,"url":null,"abstract":"<p><p>Fifteen undescribed polyketides aculeatides A-O and one known compound xylarinol A were isolated from the endophytic fungus Aspergillus aculeatus. Their structures were identified by spectroscopic data, electronic circular dichroism (ECD) calculations and comparisons, Mo<sub>2</sub>(OAc)<sub>4</sub>-induced ECD, Rh<sub>2</sub>(OCOCF<sub>3</sub>)<sub>4</sub>-induced ECD, and the modified Mosher's method. Aculeatides A and B represent the first benzo[c]oxepine derivatives bearing a C6 side chain, while aculeatides C-I possessed a benzofuran ring system featuring a unique C8 side chain. Biologically, aculeatides J and K showed significant herbicidal activities with IC<sub>50</sub> values of 3.01 ± 0.40 and 3.33 ± 0.52 μM.</p>","PeriodicalId":20170,"journal":{"name":"Phytochemistry","volume":" ","pages":"114631"},"PeriodicalIF":3.4000,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Structurally diverse polyketides with herbicidal activity from the fungus Aspergillus aculeatus.\",\"authors\":\"Fei Liu, Shanshan Hong, Xiaoxia Gu, Qian Zhang, Qin Li, Weiguang Sun, Chunmei Chen, Yonghui Zhang, Hucheng Zhu\",\"doi\":\"10.1016/j.phytochem.2025.114631\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Fifteen undescribed polyketides aculeatides A-O and one known compound xylarinol A were isolated from the endophytic fungus Aspergillus aculeatus. Their structures were identified by spectroscopic data, electronic circular dichroism (ECD) calculations and comparisons, Mo<sub>2</sub>(OAc)<sub>4</sub>-induced ECD, Rh<sub>2</sub>(OCOCF<sub>3</sub>)<sub>4</sub>-induced ECD, and the modified Mosher's method. Aculeatides A and B represent the first benzo[c]oxepine derivatives bearing a C6 side chain, while aculeatides C-I possessed a benzofuran ring system featuring a unique C8 side chain. Biologically, aculeatides J and K showed significant herbicidal activities with IC<sub>50</sub> values of 3.01 ± 0.40 and 3.33 ± 0.52 μM.</p>\",\"PeriodicalId\":20170,\"journal\":{\"name\":\"Phytochemistry\",\"volume\":\" \",\"pages\":\"114631\"},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2025-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Phytochemistry\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1016/j.phytochem.2025.114631\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/8/5 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.phytochem.2025.114631","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/5 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Structurally diverse polyketides with herbicidal activity from the fungus Aspergillus aculeatus.
Fifteen undescribed polyketides aculeatides A-O and one known compound xylarinol A were isolated from the endophytic fungus Aspergillus aculeatus. Their structures were identified by spectroscopic data, electronic circular dichroism (ECD) calculations and comparisons, Mo2(OAc)4-induced ECD, Rh2(OCOCF3)4-induced ECD, and the modified Mosher's method. Aculeatides A and B represent the first benzo[c]oxepine derivatives bearing a C6 side chain, while aculeatides C-I possessed a benzofuran ring system featuring a unique C8 side chain. Biologically, aculeatides J and K showed significant herbicidal activities with IC50 values of 3.01 ± 0.40 and 3.33 ± 0.52 μM.
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.