{"title":"药用植物古蓼根际真菌克宁木霉抗炎活性的聚酮类化合物研究","authors":"Liping Huang, Mengsha Wei, Lanqin Li, Qin Li, Weiguang Sun, Xiaotan Yu, Fengqing Wang, Zhengxi Hu, Chunmei Chen*, Hucheng Zhu* and Yonghui Zhang*, ","doi":"10.1021/acs.jnatprod.2c00842","DOIUrl":null,"url":null,"abstract":"<p >Twelve new fungal polyketides, koningiopisins I–P (<b>1</b>–<b>8</b>) and trichoketides C–F (<b>9</b>–<b>12</b>), together with six known congeners (<b>13</b>–<b>18</b>), were isolated from <i>Trichoderma koningiopsis</i>, a rhizosphere fungus obtained from the medicinal plant <i>Polygonum paleaceum</i>. Their structures and absolute configurations were established by spectroscopic analysis, single-crystal X-ray diffraction, the modified Mosher’s method, chemical derivatization, the octant rule, and <sup>13</sup>C NMR and ECD calculations. Compounds <b>1</b>–<b>5</b> are tricyclic polyketides possessing an octahydrochromene framework with a 6,8-dioxabicyclo[3.2.1]octane core. Compounds <b>7</b> and <b>8</b> contain a unique ketone carbonyl group at C-7 and differ from other members of this group of compounds with the ketone carbonyl group at C-1. Compounds <b>1</b>, <b>2</b>, and <b>13</b> showed inhibitory activity on LPS-induced BV-2 cells on NO production with IC<sub>50</sub> values of 14 ± 1, 3.0 ± 0.5, and 8.9 ± 2.7 μM, respectively.</p>","PeriodicalId":47,"journal":{"name":"Journal of Natural Products ","volume":"86 7","pages":"1643–1653"},"PeriodicalIF":3.3000,"publicationDate":"2023-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Polyketides with Anti-Inflammatory Activity from Trichoderma koningiopsis, a Rhizosphere Fungus from the Medicinal Plant Polygonum paleaceum\",\"authors\":\"Liping Huang, Mengsha Wei, Lanqin Li, Qin Li, Weiguang Sun, Xiaotan Yu, Fengqing Wang, Zhengxi Hu, Chunmei Chen*, Hucheng Zhu* and Yonghui Zhang*, \",\"doi\":\"10.1021/acs.jnatprod.2c00842\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Twelve new fungal polyketides, koningiopisins I–P (<b>1</b>–<b>8</b>) and trichoketides C–F (<b>9</b>–<b>12</b>), together with six known congeners (<b>13</b>–<b>18</b>), were isolated from <i>Trichoderma koningiopsis</i>, a rhizosphere fungus obtained from the medicinal plant <i>Polygonum paleaceum</i>. Their structures and absolute configurations were established by spectroscopic analysis, single-crystal X-ray diffraction, the modified Mosher’s method, chemical derivatization, the octant rule, and <sup>13</sup>C NMR and ECD calculations. Compounds <b>1</b>–<b>5</b> are tricyclic polyketides possessing an octahydrochromene framework with a 6,8-dioxabicyclo[3.2.1]octane core. Compounds <b>7</b> and <b>8</b> contain a unique ketone carbonyl group at C-7 and differ from other members of this group of compounds with the ketone carbonyl group at C-1. Compounds <b>1</b>, <b>2</b>, and <b>13</b> showed inhibitory activity on LPS-induced BV-2 cells on NO production with IC<sub>50</sub> values of 14 ± 1, 3.0 ± 0.5, and 8.9 ± 2.7 μM, respectively.</p>\",\"PeriodicalId\":47,\"journal\":{\"name\":\"Journal of Natural Products \",\"volume\":\"86 7\",\"pages\":\"1643–1653\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2023-07-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Natural Products \",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.jnatprod.2c00842\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Natural Products ","FirstCategoryId":"99","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jnatprod.2c00842","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Polyketides with Anti-Inflammatory Activity from Trichoderma koningiopsis, a Rhizosphere Fungus from the Medicinal Plant Polygonum paleaceum
Twelve new fungal polyketides, koningiopisins I–P (1–8) and trichoketides C–F (9–12), together with six known congeners (13–18), were isolated from Trichoderma koningiopsis, a rhizosphere fungus obtained from the medicinal plant Polygonum paleaceum. Their structures and absolute configurations were established by spectroscopic analysis, single-crystal X-ray diffraction, the modified Mosher’s method, chemical derivatization, the octant rule, and 13C NMR and ECD calculations. Compounds 1–5 are tricyclic polyketides possessing an octahydrochromene framework with a 6,8-dioxabicyclo[3.2.1]octane core. Compounds 7 and 8 contain a unique ketone carbonyl group at C-7 and differ from other members of this group of compounds with the ketone carbonyl group at C-1. Compounds 1, 2, and 13 showed inhibitory activity on LPS-induced BV-2 cells on NO production with IC50 values of 14 ± 1, 3.0 ± 0.5, and 8.9 ± 2.7 μM, respectively.
期刊介绍:
The Journal of Natural Products invites and publishes papers that make substantial and scholarly contributions to the area of natural products research. Contributions may relate to the chemistry and/or biochemistry of naturally occurring compounds or the biology of living systems from which they are obtained.
Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.
When new compounds are reported, manuscripts describing their biological activity are much preferred.
Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.