Huiqin Chen , Hao Zheng , Caihong Cai , Hao Wang , Cuijuan Gai , Zhiqiong Tan , Haofu Dai , Wenli Mei
{"title":"源自 Nerium indicum 叶子的内生真菌 Colletotruchum sp.","authors":"Huiqin Chen , Hao Zheng , Caihong Cai , Hao Wang , Cuijuan Gai , Zhiqiong Tan , Haofu Dai , Wenli Mei","doi":"10.1016/j.chmed.2023.07.004","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p>To study secondary metabolites from endophytic fungus <em>Colletotruchum</em> sp. HK-08 originated from the leaves of <em>Nerium indicum</em>.</p></div><div><h3>Methods</h3><p>The compounds were isolated by various column chromatographic techniques, and their structures were elucidated by spectroscopic techniques [high resolution electrospray ionization mass spectroscopy (HRESIMS), one-dimensional (1D) and two-dimensional (2D) nuclear magnetic resonance spectroscopy (NMR)], as well as comparison with literature data. The Ellman method was used to determine the acetylcholinesterase (AChE) inhibitory activity.</p></div><div><h3>Results</h3><p>Four indole derivatives were identified from <em>Colletotruchum</em> sp. HK-08, including 6<em>′-</em>hydroxymonaspiloindole (<strong>1</strong>), 2-(2-oxoindolin-3-yl)ethyl 2-(4-hydroxyphenyl) acetate (<strong>2</strong>), 2-(2-oxoindolin-3-yl)ethyl 2-(2-hydroxyphenyl)acetate (<strong>3</strong>), and monaspiloindole (<strong>4</strong>). Compound <strong>4</strong> presented weak AChE inhibitory activity with IC<sub>50</sub> value of (69.30 ± 6.27) μmol/L [tacrine as the positive control, with IC<sub>50</sub> value of (0.61 ± 0.07) μmol/L].</p></div><div><h3>Conclusion</h3><p>Compounds <strong>1–3</strong> were new compounds, and compound <strong>4</strong> had weak AChE inhibitory activity.</p></div>","PeriodicalId":9916,"journal":{"name":"Chinese Herbal Medicines","volume":"16 2","pages":"Pages 235-238"},"PeriodicalIF":4.7000,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1674638424000054/pdfft?md5=3293dee1afdfcb765876b62d62f1c458&pid=1-s2.0-S1674638424000054-main.pdf","citationCount":"0","resultStr":"{\"title\":\"New indole derivatives from endophytic fungus Colletotruchum sp. HK-08 originated from leaves of Nerium indicum\",\"authors\":\"Huiqin Chen , Hao Zheng , Caihong Cai , Hao Wang , Cuijuan Gai , Zhiqiong Tan , Haofu Dai , Wenli Mei\",\"doi\":\"10.1016/j.chmed.2023.07.004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><p>To study secondary metabolites from endophytic fungus <em>Colletotruchum</em> sp. HK-08 originated from the leaves of <em>Nerium indicum</em>.</p></div><div><h3>Methods</h3><p>The compounds were isolated by various column chromatographic techniques, and their structures were elucidated by spectroscopic techniques [high resolution electrospray ionization mass spectroscopy (HRESIMS), one-dimensional (1D) and two-dimensional (2D) nuclear magnetic resonance spectroscopy (NMR)], as well as comparison with literature data. The Ellman method was used to determine the acetylcholinesterase (AChE) inhibitory activity.</p></div><div><h3>Results</h3><p>Four indole derivatives were identified from <em>Colletotruchum</em> sp. HK-08, including 6<em>′-</em>hydroxymonaspiloindole (<strong>1</strong>), 2-(2-oxoindolin-3-yl)ethyl 2-(4-hydroxyphenyl) acetate (<strong>2</strong>), 2-(2-oxoindolin-3-yl)ethyl 2-(2-hydroxyphenyl)acetate (<strong>3</strong>), and monaspiloindole (<strong>4</strong>). Compound <strong>4</strong> presented weak AChE inhibitory activity with IC<sub>50</sub> value of (69.30 ± 6.27) μmol/L [tacrine as the positive control, with IC<sub>50</sub> value of (0.61 ± 0.07) μmol/L].</p></div><div><h3>Conclusion</h3><p>Compounds <strong>1–3</strong> were new compounds, and compound <strong>4</strong> had weak AChE inhibitory activity.</p></div>\",\"PeriodicalId\":9916,\"journal\":{\"name\":\"Chinese Herbal Medicines\",\"volume\":\"16 2\",\"pages\":\"Pages 235-238\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2024-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S1674638424000054/pdfft?md5=3293dee1afdfcb765876b62d62f1c458&pid=1-s2.0-S1674638424000054-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Herbal Medicines\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1674638424000054\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Herbal Medicines","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1674638424000054","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
New indole derivatives from endophytic fungus Colletotruchum sp. HK-08 originated from leaves of Nerium indicum
Objective
To study secondary metabolites from endophytic fungus Colletotruchum sp. HK-08 originated from the leaves of Nerium indicum.
Methods
The compounds were isolated by various column chromatographic techniques, and their structures were elucidated by spectroscopic techniques [high resolution electrospray ionization mass spectroscopy (HRESIMS), one-dimensional (1D) and two-dimensional (2D) nuclear magnetic resonance spectroscopy (NMR)], as well as comparison with literature data. The Ellman method was used to determine the acetylcholinesterase (AChE) inhibitory activity.
Results
Four indole derivatives were identified from Colletotruchum sp. HK-08, including 6′-hydroxymonaspiloindole (1), 2-(2-oxoindolin-3-yl)ethyl 2-(4-hydroxyphenyl) acetate (2), 2-(2-oxoindolin-3-yl)ethyl 2-(2-hydroxyphenyl)acetate (3), and monaspiloindole (4). Compound 4 presented weak AChE inhibitory activity with IC50 value of (69.30 ± 6.27) μmol/L [tacrine as the positive control, with IC50 value of (0.61 ± 0.07) μmol/L].
Conclusion
Compounds 1–3 were new compounds, and compound 4 had weak AChE inhibitory activity.