Cuparene-type sesquiterpenes with neuroprotective activities from the edible mushroom Flammulina filiformis

Four new cuparene-type sesquiterpenes, flammuterpenols A - D (1-4), along with one known congener (5) were isolated from the solid culture of edible mushroom Flammulina filiformis. Their structures with a benzoxabicyclo[3.2.1]octane core were elucidated by integrated multiple spectroscopic techniques, electronic circular dichroism, and single crystal X-ray diffraction analysis. Biologically, compounds 1-5 were evaluated in vitro for their neuroprotective effects against 6-hydroxydopamine induced cell death in human neuroblastoma SH-SY5Y cells. All of them exhibited remarkable neuroprotective effects possessing the EC<sub>50</sub> values ranging from 0.93 ± 0.02 to 10.28 ± 0.10 μM. These findings not only enrich the structural diversity of cuparene-type sesquiterpenes, but also provide potential candidates for the further development of the neuroprotective agents.

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Publication Details

Journal
Fitoterapia
Published
2024-09-23
DOI
https://doi.org/10.1016/j.fitote.2024.106235
Citations
2
Primary Topic
Fungal Biology and Applications
Type
article
Field-Weighted Citation Impact
0.90

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article

Cuparene-type sesquiterpenes with neuroprotective activities from the edible mushroom Flammulina filiformis

Xianqiang Chen, Qing Yan, Shouyuan Wu, Jingling Ren et al.
2 citations
Fitoterapia
Fungal Biology and Applications
0.90
article

Cuparene-type sesquiterpenes with neuroprotective activities from the edible mushroom Flammulina filiformis

Xianqiang Chen, Qing Yan, Shouyuan Wu, Jingling Ren, Ziming Chen, Peilian Liu
article en
2 citations

Abstract

Four new cuparene-type sesquiterpenes, flammuterpenols A - D (1-4), along with one known congener (5) were isolated from the solid culture of edible mushroom Flammulina filiformis. Their structures with a benzoxabicyclo[3.2.1]octane core were elucidated by integrated multiple spectroscopic techniques, electronic circular dichroism, and single crystal X-ray diffraction analysis. Biologically, compounds 1-5 were evaluated in vitro for their neuroprotective effects against 6-hydroxydopamine induced cell death in human neuroblastoma SH-SY5Y cells. All of them exhibited remarkable neuroprotective effects possessing the EC<sub>50</sub> values ranging from 0.93 ± 0.02 to 10.28 ± 0.10 μM. These findings not only enrich the structural diversity of cuparene-type sesquiterpenes, but also provide potential candidates for the further development of the neuroprotective agents.

FitoterapiaVol. 179
Guangxi University (CN), Guangxi University of Chinese Medicine (CN)
Natural Science Foundation of Guangxi Province
Zero hunger
Openalex Percentile: Top 24%
Fungal Biology and Applications
0.90
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