Bioassay-guided isolation and characterisation of α-glucosidase inhibitors from Sanghuangporus baumii.

Bioassay-guided fractionation of the isopropanol extract of the medicinal mushroom Sanghuangporus baumii led to the isolation and characterisation of a new acorane-type sesquiterpenoid bauminene (1) and seven known compounds 2–8. The planar structure of 1 was elucidated on the basis of extensive spe...

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Publicado en:Natural Product Research Vol. 39; no. 6; pp. 1452 - 1461
Autores principales: Hu, Xiaoyan, Wang, Yanling, Lin, Yuhao, Yang, Nini, Yao, Junyi, Shan, Weiguang, Rao, Guiwei, Ying, Youmin
Formato: Journal Article
Publicado: Taylor & Francis Ltd Mar2025
Acceso en línea:Ver este registro en EBSCOhost
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        14786419
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      jtl: Natural Product Research
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      dt: Mar2025
      vid: 39
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      pub: Taylor & Francis Ltd
      place: Philadelphia, Pennsylvania
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        183684350
        174597302
        10.1080/14786419.2023.2300397
        183684350
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        atl: Bioassay-guided isolation and characterisation of α-glucosidase inhibitors from Sanghuangporus baumii.
      aug:
        au:
          Hu, Xiaoyan
          Wang, Yanling
          Lin, Yuhao
          Yang, Nini
          Yao, Junyi
          Shan, Weiguang
          Rao, Guiwei
          Ying, Youmin
        affil: College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, China
      sug:
      ab: Bioassay-guided fractionation of the isopropanol extract of the medicinal mushroom Sanghuangporus baumii led to the isolation and characterisation of a new acorane-type sesquiterpenoid bauminene (1) and seven known compounds 2–8. The planar structure of 1 was elucidated on the basis of extensive spectroscopic analysis, including 1D, 2D NMR and HR-ESI-MS. The relative configuration of 1 was determined by a combination of ROESY experiment, density functional theory calculation of 13C NMR, and DP4+ probability analysis, while the absolute configuration of 1 was established by comparative electronic circular dichroism (ECD) spectra analysis. In the in vitro bioassay, compounds 1–8 exhibited potent to moderate α-glucosidase inhibitory activity with IC50 values ranging from 6.8 ± 0.68 to 221.4 ± 6.57 µM. The presences of these bioactive constituents in the sclerotia of S. baumii may be related to the use of the fungus as 'Sanghuang' for the adjuvant treatment of DM.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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