Kazuki Hashimoto, Kana Kimura, Kotaro Ishida, Eiji Morita, Kazuaki Tanaka and Masaru Hashimoto*,
{"title":"HIV-1整合酶抑制剂二氢obionin B及其特异性旋转的研究","authors":"Kazuki Hashimoto, Kana Kimura, Kotaro Ishida, Eiji Morita, Kazuaki Tanaka and Masaru Hashimoto*, ","doi":"10.1021/acs.jnatprod.3c00353","DOIUrl":null,"url":null,"abstract":"<p >Dihydroobionin B (<b>1</b>), a chiral congener of known obionin B, was isolated from <i>Pseudocoleophoma</i> sp. KT4119, a freshwater fungus collected from a submerged wood block in Kochi Prefecture, Japan, in 2020. The planar structure of <b>1</b> was characterized by mass and NMR spectral analysis and confirmed by density functional theory (DFT)-based chemical shift calculations. Its absolute structure was determined by electronic circular dichroism spectral analysis. Notably, <b>1</b> exhibited an extraordinarily large specific rotation [[α]<sup>20</sup><sub>D</sub> +1080 (<i>c</i> 0.056, CHCl<sub>3</sub>)], which was verified by DFT-based specific rotation calculations. However, these calculations indicated that the sign of the specific rotation based on static analysis was insufficient to determine the absolute configuration in this case. Furthermore, <i>Pseudocoleophoma</i> KT4119 produced coleophomapyrones A (<b>2</b>) and B (<b>3</b>) and coleophomaldehyde A (<b>4</b>). While this is the first report of <b>2</b> isolated from a natural source, it has also been prepared previously using a synthetic approach. Compound <b>1</b> potently inhibited HIV type 1 integrase (IC<sub>50</sub> = 0.44 μM) without significant cytotoxicity. Finally, docking experiments were conducted to propose a plausible mechanism for the behavior of <b>1</b>.</p>","PeriodicalId":47,"journal":{"name":"Journal of Natural Products ","volume":"86 9","pages":"2139–2144"},"PeriodicalIF":3.3000,"publicationDate":"2023-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"HIV-1 Integrase Inhibitor, Dihydroobionin B, and the Investigation of Its Extraordinary Specific Rotation\",\"authors\":\"Kazuki Hashimoto, Kana Kimura, Kotaro Ishida, Eiji Morita, Kazuaki Tanaka and Masaru Hashimoto*, \",\"doi\":\"10.1021/acs.jnatprod.3c00353\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Dihydroobionin B (<b>1</b>), a chiral congener of known obionin B, was isolated from <i>Pseudocoleophoma</i> sp. KT4119, a freshwater fungus collected from a submerged wood block in Kochi Prefecture, Japan, in 2020. The planar structure of <b>1</b> was characterized by mass and NMR spectral analysis and confirmed by density functional theory (DFT)-based chemical shift calculations. Its absolute structure was determined by electronic circular dichroism spectral analysis. Notably, <b>1</b> exhibited an extraordinarily large specific rotation [[α]<sup>20</sup><sub>D</sub> +1080 (<i>c</i> 0.056, CHCl<sub>3</sub>)], which was verified by DFT-based specific rotation calculations. However, these calculations indicated that the sign of the specific rotation based on static analysis was insufficient to determine the absolute configuration in this case. Furthermore, <i>Pseudocoleophoma</i> KT4119 produced coleophomapyrones A (<b>2</b>) and B (<b>3</b>) and coleophomaldehyde A (<b>4</b>). While this is the first report of <b>2</b> isolated from a natural source, it has also been prepared previously using a synthetic approach. Compound <b>1</b> potently inhibited HIV type 1 integrase (IC<sub>50</sub> = 0.44 μM) without significant cytotoxicity. Finally, docking experiments were conducted to propose a plausible mechanism for the behavior of <b>1</b>.</p>\",\"PeriodicalId\":47,\"journal\":{\"name\":\"Journal of Natural Products \",\"volume\":\"86 9\",\"pages\":\"2139–2144\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2023-08-18\",\"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.3c00353\",\"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.3c00353","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
HIV-1 Integrase Inhibitor, Dihydroobionin B, and the Investigation of Its Extraordinary Specific Rotation
Dihydroobionin B (1), a chiral congener of known obionin B, was isolated from Pseudocoleophoma sp. KT4119, a freshwater fungus collected from a submerged wood block in Kochi Prefecture, Japan, in 2020. The planar structure of 1 was characterized by mass and NMR spectral analysis and confirmed by density functional theory (DFT)-based chemical shift calculations. Its absolute structure was determined by electronic circular dichroism spectral analysis. Notably, 1 exhibited an extraordinarily large specific rotation [[α]20D +1080 (c 0.056, CHCl3)], which was verified by DFT-based specific rotation calculations. However, these calculations indicated that the sign of the specific rotation based on static analysis was insufficient to determine the absolute configuration in this case. Furthermore, Pseudocoleophoma KT4119 produced coleophomapyrones A (2) and B (3) and coleophomaldehyde A (4). While this is the first report of 2 isolated from a natural source, it has also been prepared previously using a synthetic approach. Compound 1 potently inhibited HIV type 1 integrase (IC50 = 0.44 μM) without significant cytotoxicity. Finally, docking experiments were conducted to propose a plausible mechanism for the behavior of 1.
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.