{"title":"从蘑菇 Lanmaoa asiatica 中分离出的真菌 Pestalotiopsis clavata JSQ 12 的两种烯基苯酚衍生物。","authors":"Jing Tang, Rui Xu, Hao Ma, Shuai-Ming Zhu, Fu-Yao Luo, Xue Zhao, Ya-Shuai Kang, Yuan-Wei Gao, Yu Yang, Chang-Wei Li","doi":"10.1080/14786419.2024.2367012","DOIUrl":null,"url":null,"abstract":"<p><p>Two new alkenyl phenol derivatives, namely pestalol F (<b>1</b>) and pestalol G (<b>2</b>), along with two known compounds, pestalachloride A (<b>3</b>) and pestalotiopsin J (<b>4</b>), were isolated from the culture of the fungus <i>Pestalotiopsis clavata</i> JSQ 12. The structures of these compounds were primarily elucidated by MS, NMR and specific rotation data analysises. These secondary metabolites of <i>Pestalotiopsis clavata</i> were reported for the first time. Compound <b>2</b> displayed interesting cytotoxic activity against MCF-7 cell line with the IC<sub>50</sub> value of 29.16 μM, whereas compound <b>3</b> exhibited moderate activity towards A549 cell line with the IC<sub>50</sub> value of 35.71 μM. The positive control 5-FU showed cytotoxic effects on MCF-7 and A549 cell lines with the respective IC<sub>50</sub> values of 26.70 and 26.07 μM. Compounds <b>1</b> and <b>2</b> displayed mild antibacterial activities against <i>Staphylococcus aureus</i> with MIC values of 128 and 64 μg/mL (MIC of positive control, penicillin, was 0.016 μg/mL), respectively.</p>","PeriodicalId":18990,"journal":{"name":"Natural Product Research","volume":" ","pages":"4488-4492"},"PeriodicalIF":1.6000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Two alkenyl phenol derivatives from the fungus <i>Pestalotiopsis clavata</i> JSQ 12 isolated from the mushroom <i>Lanmaoa asiatica</i>.\",\"authors\":\"Jing Tang, Rui Xu, Hao Ma, Shuai-Ming Zhu, Fu-Yao Luo, Xue Zhao, Ya-Shuai Kang, Yuan-Wei Gao, Yu Yang, Chang-Wei Li\",\"doi\":\"10.1080/14786419.2024.2367012\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Two new alkenyl phenol derivatives, namely pestalol F (<b>1</b>) and pestalol G (<b>2</b>), along with two known compounds, pestalachloride A (<b>3</b>) and pestalotiopsin J (<b>4</b>), were isolated from the culture of the fungus <i>Pestalotiopsis clavata</i> JSQ 12. The structures of these compounds were primarily elucidated by MS, NMR and specific rotation data analysises. These secondary metabolites of <i>Pestalotiopsis clavata</i> were reported for the first time. Compound <b>2</b> displayed interesting cytotoxic activity against MCF-7 cell line with the IC<sub>50</sub> value of 29.16 μM, whereas compound <b>3</b> exhibited moderate activity towards A549 cell line with the IC<sub>50</sub> value of 35.71 μM. The positive control 5-FU showed cytotoxic effects on MCF-7 and A549 cell lines with the respective IC<sub>50</sub> values of 26.70 and 26.07 μM. Compounds <b>1</b> and <b>2</b> displayed mild antibacterial activities against <i>Staphylococcus aureus</i> with MIC values of 128 and 64 μg/mL (MIC of positive control, penicillin, was 0.016 μg/mL), respectively.</p>\",\"PeriodicalId\":18990,\"journal\":{\"name\":\"Natural Product Research\",\"volume\":\" \",\"pages\":\"4488-4492\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2025-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Natural Product Research\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1080/14786419.2024.2367012\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/6/13 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural Product Research","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1080/14786419.2024.2367012","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/6/13 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Two alkenyl phenol derivatives from the fungus Pestalotiopsis clavata JSQ 12 isolated from the mushroom Lanmaoa asiatica.
Two new alkenyl phenol derivatives, namely pestalol F (1) and pestalol G (2), along with two known compounds, pestalachloride A (3) and pestalotiopsin J (4), were isolated from the culture of the fungus Pestalotiopsis clavata JSQ 12. The structures of these compounds were primarily elucidated by MS, NMR and specific rotation data analysises. These secondary metabolites of Pestalotiopsis clavata were reported for the first time. Compound 2 displayed interesting cytotoxic activity against MCF-7 cell line with the IC50 value of 29.16 μM, whereas compound 3 exhibited moderate activity towards A549 cell line with the IC50 value of 35.71 μM. The positive control 5-FU showed cytotoxic effects on MCF-7 and A549 cell lines with the respective IC50 values of 26.70 and 26.07 μM. Compounds 1 and 2 displayed mild antibacterial activities against Staphylococcus aureus with MIC values of 128 and 64 μg/mL (MIC of positive control, penicillin, was 0.016 μg/mL), respectively.
期刊介绍:
The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds.
The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal.
Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section.
All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.