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  1. 学術雑誌論文

Isolation, structural determination, and antiviral activities of metabolites from vanitaracin A-producing Talaromyces sp

https://az.repo.nii.ac.jp/records/2000364
https://az.repo.nii.ac.jp/records/2000364
34a5d581-21d8-47d1-bbd7-31987a34036e
名前 / ファイル ライセンス アクション
Kamisuki Kamisuki JA2023.pdf (411 KB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2025-03-14
タイトル
タイトル Isolation, structural determination, and antiviral activities of metabolites from vanitaracin A-producing Talaromyces sp
言語 en
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Kamisuki, Shinji

× Kamisuki, Shinji

en Kamisuki, Shinji

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Shibasaki, Hisanobu

× Shibasaki, Hisanobu

en Shibasaki, Hisanobu

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Murakami, Hironobu

× Murakami, Hironobu

en Murakami, Hironobu

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Fujino, Kan

× Fujino, Kan

en Fujino, Kan

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Tsukuda, Senko

× Tsukuda, Senko

en Tsukuda, Senko

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Kojima, Ikumi

× Kojima, Ikumi

en Kojima, Ikumi

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Ashikawa, Koudai

× Ashikawa, Koudai

en Ashikawa, Koudai

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Kanno, Kazuki

× Kanno, Kazuki

en Kanno, Kazuki

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Ishikawa, Tomohiro

× Ishikawa, Tomohiro

en Ishikawa, Tomohiro

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Saito, Tatsuo

× Saito, Tatsuo

en Saito, Tatsuo

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Sugawara, Fumio

× Sugawara, Fumio

en Sugawara, Fumio

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Watashi, Koichi

× Watashi, Koichi

en Watashi, Koichi

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Kuramochi, Kouji

× Kuramochi, Kouji

en Kuramochi, Kouji

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抄録
内容記述タイプ Abstract
Abstract
内容記述タイプ Abstract
内容記述 Vanitaracin A, an anti-hepatitis B virus polyketide, has been previously isolated from Talaromyces sp. In the present study, we searched for novel compounds in the culture broth obtained from a vanitaracin A-producing fungus under various conditions. Three novel compounds (vanitaracin C, vanitaraphilone A, and 2-hydroxy-4(hydroxymethyl)-6-methylbenzaldehyde) were isolated, and their structures were determined using spectroscopic methods (1D/2D NMR and MS). In addition, the antiviral spectrum of vanitaracin A was examined by measuring its antiviral activities against rabies virus, Borna disease virus 1, and bovine leukemia virus. This compound exhibited antiviral activity against bovine leukemia virus, which is the causative agent of enzootic bovine leukosis. The anti-bovine leukemia virus effects of other compounds isolated from the vanitaracin A-producing fungus, namely, vanitaracins B and C, vanitaraphilone A, and 2-hydroxy-4-(hydroxymethyl)-6-methylbenzaldehyde, were also evaluated. Vanitaracin B, vanitaraphilone A and 2-hydroxy-4-(hydroxymethyl)-6methylbenzaldehyde were also found to exhibit activity against bovine leukemia virus. These findings reveal the broad-spectrum antiviral activity of the vanitaracin scaffold and suggest several candidates for the development of anti-bovine leukemia virus drugs.
言語 en
bibliographic_information The Journal of antibiotics

巻 76, 号 2, p. 75-82, 発行日 2023-02
出版者
出版者 Springer Nature
item_10002_relation_14
識別子タイプ DOI
関連識別子 10.1038/s41429-022-00585-9
出版タイプ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
item_1730428627434
内容記述タイプ Other
内容記述 査読あり
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