{"title":"内生真菌孢毛镰刀菌的一个新的四环三萜","authors":"Yajing Wang, Chunyue Liu, Yihui Yang, Chang Li, Yuehu Pei","doi":"10.1016/j.chmed.2022.10.007","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p>To isolate bioactive compounds from the endophytic fungus <em>Fusarium sporotrichioides</em> isolated from <em>Rauwolfia yunnanensis</em>, and investigate their pharmacological activities.</p></div><div><h3>Methods</h3><p>The chemical constituents were isolated and purified by combining with ODS column chromatography, silica gel column chromatography and by performing semipreparative HPLC. Their structures were established on the basis of 1D NMR (<sup>1</sup>H-NMR and <sup>13</sup>C-NMR) and 2D NMR (<sup>1</sup>H–<sup>1</sup>H COSY, HSQC, HMBC and NOESY), as well as HRESIMS and comparison with literature data. In addition, the absolute configuration of compound <strong>1</strong> was determined by calculated ECD data.</p></div><div><h3>Results</h3><p>One previously undescribed tetracyclic triterpenoid derivative, named as integracide L (<strong>1</strong>), 12<em>α</em>-acetoxy-4,4-dimethyl-24-methylene-5<em>α</em>-cholesta-8,14-diene-2<em>α</em>,3<em>β</em>,11<em>β</em>-triol (<strong>2</strong>), 12<em>α</em>-acetoxy-4,4-dimethyl-24-methylene-5<em>α</em>-cholesta-8-momoene-2<em>α</em>,3<em>β</em>,11<em>β</em>-triol (<strong>3</strong>), 12<em>α</em>-acetoxy-4,4-dimethyl-24-methylene-5<em>α</em>-cholesta-8,14-diene-3<em>β</em>,11<em>β</em>-triol (<strong>4</strong>), and 12<em>α</em>-acetoxy-4,4-dimethyl-24-methylene-5<em>α</em>-cholesta-8-momoene-3<em>β</em>,11<em>β</em>-triol (<strong>5</strong>) were isolated from <em>F. sporotrichioide</em>. Moreover, compound <strong>1</strong> was rare tetracyclic triterpenoid with single methyl replacement at C-4 position.</p></div><div><h3>Conclusion</h3><p>Compound <strong>1</strong> was a new tetracyclic triterpenoid isolated from the endophytic fungus <em>F. sporotrichioides.</em> In addition, compound <strong>2</strong> could inhibit the growth of three different human cancer cells significantly. Compounds <strong>3</strong> and <strong>5</strong> were found to possess better cytotoxic activities on HepG-2 cells than the other compounds, with IC<sub>50</sub> values of (2.8 ± 0.1) and (6.3 ± 0.3) μmol/L respectively.</p></div>","PeriodicalId":9916,"journal":{"name":"Chinese Herbal Medicines","volume":"16 2","pages":"Pages 231-234"},"PeriodicalIF":4.7000,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1674638423000497/pdfft?md5=c01ee69ebdd540fb5907795d661bfd93&pid=1-s2.0-S1674638423000497-main.pdf","citationCount":"0","resultStr":"{\"title\":\"A new tetracyclic triterpenoid from endophytic fungus Fusarium sporotrichioides\",\"authors\":\"Yajing Wang, Chunyue Liu, Yihui Yang, Chang Li, Yuehu Pei\",\"doi\":\"10.1016/j.chmed.2022.10.007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><p>To isolate bioactive compounds from the endophytic fungus <em>Fusarium sporotrichioides</em> isolated from <em>Rauwolfia yunnanensis</em>, and investigate their pharmacological activities.</p></div><div><h3>Methods</h3><p>The chemical constituents were isolated and purified by combining with ODS column chromatography, silica gel column chromatography and by performing semipreparative HPLC. Their structures were established on the basis of 1D NMR (<sup>1</sup>H-NMR and <sup>13</sup>C-NMR) and 2D NMR (<sup>1</sup>H–<sup>1</sup>H COSY, HSQC, HMBC and NOESY), as well as HRESIMS and comparison with literature data. In addition, the absolute configuration of compound <strong>1</strong> was determined by calculated ECD data.</p></div><div><h3>Results</h3><p>One previously undescribed tetracyclic triterpenoid derivative, named as integracide L (<strong>1</strong>), 12<em>α</em>-acetoxy-4,4-dimethyl-24-methylene-5<em>α</em>-cholesta-8,14-diene-2<em>α</em>,3<em>β</em>,11<em>β</em>-triol (<strong>2</strong>), 12<em>α</em>-acetoxy-4,4-dimethyl-24-methylene-5<em>α</em>-cholesta-8-momoene-2<em>α</em>,3<em>β</em>,11<em>β</em>-triol (<strong>3</strong>), 12<em>α</em>-acetoxy-4,4-dimethyl-24-methylene-5<em>α</em>-cholesta-8,14-diene-3<em>β</em>,11<em>β</em>-triol (<strong>4</strong>), and 12<em>α</em>-acetoxy-4,4-dimethyl-24-methylene-5<em>α</em>-cholesta-8-momoene-3<em>β</em>,11<em>β</em>-triol (<strong>5</strong>) were isolated from <em>F. sporotrichioide</em>. Moreover, compound <strong>1</strong> was rare tetracyclic triterpenoid with single methyl replacement at C-4 position.</p></div><div><h3>Conclusion</h3><p>Compound <strong>1</strong> was a new tetracyclic triterpenoid isolated from the endophytic fungus <em>F. sporotrichioides.</em> In addition, compound <strong>2</strong> could inhibit the growth of three different human cancer cells significantly. Compounds <strong>3</strong> and <strong>5</strong> were found to possess better cytotoxic activities on HepG-2 cells than the other compounds, with IC<sub>50</sub> values of (2.8 ± 0.1) and (6.3 ± 0.3) μmol/L respectively.</p></div>\",\"PeriodicalId\":9916,\"journal\":{\"name\":\"Chinese Herbal Medicines\",\"volume\":\"16 2\",\"pages\":\"Pages 231-234\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2024-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S1674638423000497/pdfft?md5=c01ee69ebdd540fb5907795d661bfd93&pid=1-s2.0-S1674638423000497-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Herbal Medicines\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1674638423000497\",\"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/S1674638423000497","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
A new tetracyclic triterpenoid from endophytic fungus Fusarium sporotrichioides
Objective
To isolate bioactive compounds from the endophytic fungus Fusarium sporotrichioides isolated from Rauwolfia yunnanensis, and investigate their pharmacological activities.
Methods
The chemical constituents were isolated and purified by combining with ODS column chromatography, silica gel column chromatography and by performing semipreparative HPLC. Their structures were established on the basis of 1D NMR (1H-NMR and 13C-NMR) and 2D NMR (1H–1H COSY, HSQC, HMBC and NOESY), as well as HRESIMS and comparison with literature data. In addition, the absolute configuration of compound 1 was determined by calculated ECD data.
Results
One previously undescribed tetracyclic triterpenoid derivative, named as integracide L (1), 12α-acetoxy-4,4-dimethyl-24-methylene-5α-cholesta-8,14-diene-2α,3β,11β-triol (2), 12α-acetoxy-4,4-dimethyl-24-methylene-5α-cholesta-8-momoene-2α,3β,11β-triol (3), 12α-acetoxy-4,4-dimethyl-24-methylene-5α-cholesta-8,14-diene-3β,11β-triol (4), and 12α-acetoxy-4,4-dimethyl-24-methylene-5α-cholesta-8-momoene-3β,11β-triol (5) were isolated from F. sporotrichioide. Moreover, compound 1 was rare tetracyclic triterpenoid with single methyl replacement at C-4 position.
Conclusion
Compound 1 was a new tetracyclic triterpenoid isolated from the endophytic fungus F. sporotrichioides. In addition, compound 2 could inhibit the growth of three different human cancer cells significantly. Compounds 3 and 5 were found to possess better cytotoxic activities on HepG-2 cells than the other compounds, with IC50 values of (2.8 ± 0.1) and (6.3 ± 0.3) μmol/L respectively.
期刊介绍：
Chinese Herbal Medicines is intended to disseminate the latest developments and research progress in traditional and herbal medical sciences to researchers, practitioners, academics and administrators worldwide in the field of traditional and herbal medicines. The journal's international coverage ensures that research and progress from all regions of the world are widely included.
CHM is a core journal of Chinese science and technology. The journal entered into the ESCI database in 2017, and then was included in PMC, Scopus and other important international search systems. In 2019, CHM was successfully selected for the “China Science and Technology Journal Excellence Action Plan” project, which has markedly improved its international influence and industry popularity. CHM obtained the first impact factor of 3.8 in Journal Citation Reports (JCR) in 2023.
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