{"title":"Adpressins A-G: Oligophenalenone Dimers from Talaromyces adpressus.","authors":"Meijia Zheng, Qin Li, Hong Liao, Yongqi Li, Chenxi Zhou, Xinyi Zhao, Chunmei Chen, Weiguang Sun, Yonghui Zhang, Hucheng Zhu","doi":"10.1021/acs.jnatprod.4c00330","DOIUrl":null,"url":null,"abstract":"<p><p>Nine new oligophenalenone dimers, adpressins A-G (<b>1</b>-<b>9</b>), together with nine known compounds (<b>10</b>-<b>18</b>), were isolated from the fungus <i>Talaromyces adpressus</i>. Their chemical structures were determined on the basis of spectroscopic and mass spectral analyses. Their relative and absolute configurations were identified by <sup>1</sup>H and <sup>13</sup>C NMR calculations followed by DP4+ analyses, electronic circular dichroism (ECD) calculations, and ECD spectra comparison with related compounds. Compound <b>1</b> is the first example of a duclauxin derivative featuring an unusual 6/6/6/5/6/6/6 ring system, while compounds <b>6</b> and <b>7</b> contained a novel pyrrolidine ring. Compounds <b>5</b>, <b>9</b>, and <b>18</b> exhibited moderate inhibition against LPS-induced B lymphocyte proliferation with IC<sub>50</sub> values ranging from 1.6 to 8.6 <i>μ</i>M. Additionally, compounds <b>9</b> and <b>18</b> exhibited moderate inhibition against Con A-induced T lymphocyte proliferation with IC<sub>50</sub> values of 9.3 and 2.6 <i>μ</i>M, respectively.</p>","PeriodicalId":47,"journal":{"name":"Journal of Natural Products ","volume":" ","pages":"1921-1929"},"PeriodicalIF":3.3000,"publicationDate":"2024-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Adpressins A-G: Oligophenalenone Dimers from <i>Talaromyces adpressus</i>.\",\"authors\":\"Meijia Zheng, Qin Li, Hong Liao, Yongqi Li, Chenxi Zhou, Xinyi Zhao, Chunmei Chen, Weiguang Sun, Yonghui Zhang, Hucheng Zhu\",\"doi\":\"10.1021/acs.jnatprod.4c00330\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Nine new oligophenalenone dimers, adpressins A-G (<b>1</b>-<b>9</b>), together with nine known compounds (<b>10</b>-<b>18</b>), were isolated from the fungus <i>Talaromyces adpressus</i>. Their chemical structures were determined on the basis of spectroscopic and mass spectral analyses. Their relative and absolute configurations were identified by <sup>1</sup>H and <sup>13</sup>C NMR calculations followed by DP4+ analyses, electronic circular dichroism (ECD) calculations, and ECD spectra comparison with related compounds. Compound <b>1</b> is the first example of a duclauxin derivative featuring an unusual 6/6/6/5/6/6/6 ring system, while compounds <b>6</b> and <b>7</b> contained a novel pyrrolidine ring. Compounds <b>5</b>, <b>9</b>, and <b>18</b> exhibited moderate inhibition against LPS-induced B lymphocyte proliferation with IC<sub>50</sub> values ranging from 1.6 to 8.6 <i>μ</i>M. Additionally, compounds <b>9</b> and <b>18</b> exhibited moderate inhibition against Con A-induced T lymphocyte proliferation with IC<sub>50</sub> values of 9.3 and 2.6 <i>μ</i>M, respectively.</p>\",\"PeriodicalId\":47,\"journal\":{\"name\":\"Journal of Natural Products \",\"volume\":\" \",\"pages\":\"1921-1929\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2024-08-23\",\"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://doi.org/10.1021/acs.jnatprod.4c00330\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/7/21 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Natural Products ","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1021/acs.jnatprod.4c00330","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/21 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Adpressins A-G: Oligophenalenone Dimers from Talaromyces adpressus.
Nine new oligophenalenone dimers, adpressins A-G (1-9), together with nine known compounds (10-18), were isolated from the fungus Talaromyces adpressus. Their chemical structures were determined on the basis of spectroscopic and mass spectral analyses. Their relative and absolute configurations were identified by 1H and 13C NMR calculations followed by DP4+ analyses, electronic circular dichroism (ECD) calculations, and ECD spectra comparison with related compounds. Compound 1 is the first example of a duclauxin derivative featuring an unusual 6/6/6/5/6/6/6 ring system, while compounds 6 and 7 contained a novel pyrrolidine ring. Compounds 5, 9, and 18 exhibited moderate inhibition against LPS-induced B lymphocyte proliferation with IC50 values ranging from 1.6 to 8.6 μM. Additionally, compounds 9 and 18 exhibited moderate inhibition against Con A-induced T lymphocyte proliferation with IC50 values of 9.3 and 2.6 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.