{"title":"内生真菌球茶菰 BCC71876 的抗疟和抗菌物质。","authors":"Nantiya Bunbamrung, Chakapong Intaraudom, Aibrohim Dramae, Nattawut Boonyuen, Wilunda Choowong, Pranee Rachtawee, Chitti Thawai, Pattama Pittayakhajonwut","doi":"10.1080/14786419.2024.2440800","DOIUrl":null,"url":null,"abstract":"<p><p>Three previously undescribed compounds including 2',3'-dihydroxy-4,5',4″-trimethoxy-<i>p</i>-terphenyl (<b>1</b>), 5-methoxyhydroperoxyco-chliodinol (<b>2</b>), and 5-(3',3'-dimethylallyl)indole-3-oxoacetic acid (<b>17</b>), along with fifteen known compounds (<b>3</b> - <b>16</b> and <b>18</b>), were isolated from the endophytic fungus, <i>Chaetomium globosum</i> BCC71876. The chemical structures were determined by NMR spectral information as well as the comparison with those closely related compounds reported in the literature. The compounds isolated were evaluated for biological properties including antimalarial, anti-TB, anti-plant pathogenic fungal, antibacterial, and cytotoxicity. The isolated compounds exhibited a wide range of biological activities against the tested cell lines and showed very low cytotoxicity against both cancerous (MCF-7 and NCI-H187) and non-cancerous (Vero) cells, except for compounds <b>5</b>, <b>10</b>, <b>11</b>, <b>17</b>, and <b>18</b> (IC<sub>50</sub> 0.47 - 114.8 µM). Cochliodinol (<b>5</b>) had the strongest antimalarial activity (IC<sub>50</sub> 4.39 µM), whereas chaetomugilin J (<b>11</b>) showed the strongest anti-TB activity (MIC 3.13 µg/mL).</p>","PeriodicalId":18990,"journal":{"name":"Natural Product Research","volume":" ","pages":"1-10"},"PeriodicalIF":1.9000,"publicationDate":"2024-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Antimalarial and antimicrobial substances from the endophytic fungus <i>Chaetomium globosum</i> BCC71876.\",\"authors\":\"Nantiya Bunbamrung, Chakapong Intaraudom, Aibrohim Dramae, Nattawut Boonyuen, Wilunda Choowong, Pranee Rachtawee, Chitti Thawai, Pattama Pittayakhajonwut\",\"doi\":\"10.1080/14786419.2024.2440800\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Three previously undescribed compounds including 2',3'-dihydroxy-4,5',4″-trimethoxy-<i>p</i>-terphenyl (<b>1</b>), 5-methoxyhydroperoxyco-chliodinol (<b>2</b>), and 5-(3',3'-dimethylallyl)indole-3-oxoacetic acid (<b>17</b>), along with fifteen known compounds (<b>3</b> - <b>16</b> and <b>18</b>), were isolated from the endophytic fungus, <i>Chaetomium globosum</i> BCC71876. The chemical structures were determined by NMR spectral information as well as the comparison with those closely related compounds reported in the literature. The compounds isolated were evaluated for biological properties including antimalarial, anti-TB, anti-plant pathogenic fungal, antibacterial, and cytotoxicity. The isolated compounds exhibited a wide range of biological activities against the tested cell lines and showed very low cytotoxicity against both cancerous (MCF-7 and NCI-H187) and non-cancerous (Vero) cells, except for compounds <b>5</b>, <b>10</b>, <b>11</b>, <b>17</b>, and <b>18</b> (IC<sub>50</sub> 0.47 - 114.8 µM). Cochliodinol (<b>5</b>) had the strongest antimalarial activity (IC<sub>50</sub> 4.39 µM), whereas chaetomugilin J (<b>11</b>) showed the strongest anti-TB activity (MIC 3.13 µg/mL).</p>\",\"PeriodicalId\":18990,\"journal\":{\"name\":\"Natural Product Research\",\"volume\":\" \",\"pages\":\"1-10\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2024-12-16\",\"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/10.1080/14786419.2024.2440800\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural Product Research","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1080/14786419.2024.2440800","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Antimalarial and antimicrobial substances from the endophytic fungus Chaetomium globosum BCC71876.
Three previously undescribed compounds including 2',3'-dihydroxy-4,5',4″-trimethoxy-p-terphenyl (1), 5-methoxyhydroperoxyco-chliodinol (2), and 5-(3',3'-dimethylallyl)indole-3-oxoacetic acid (17), along with fifteen known compounds (3 - 16 and 18), were isolated from the endophytic fungus, Chaetomium globosum BCC71876. The chemical structures were determined by NMR spectral information as well as the comparison with those closely related compounds reported in the literature. The compounds isolated were evaluated for biological properties including antimalarial, anti-TB, anti-plant pathogenic fungal, antibacterial, and cytotoxicity. The isolated compounds exhibited a wide range of biological activities against the tested cell lines and showed very low cytotoxicity against both cancerous (MCF-7 and NCI-H187) and non-cancerous (Vero) cells, except for compounds 5, 10, 11, 17, and 18 (IC50 0.47 - 114.8 µM). Cochliodinol (5) had the strongest antimalarial activity (IC50 4.39 µM), whereas chaetomugilin J (11) showed the strongest anti-TB activity (MIC 3.13 µg/mL).
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.