Bioassay-guided isolation of hepatoprotective lignans from <i>Vernonia cinerea</i>: DeepSAT-driven structural elucidation and predictive mechanistic insights against drug-induced liver injury

Three new dibenzylbutane lignans, vernolignans A-C (1-3), along with three known compounds (4-6), were isolated from <i>Vernonia cinerea</i> through a bioactivity-guided isolation process. The planar structures of the new compounds (1-3) were elucidated through comprehensive analysis of HR-ESI-MS and 1D/2D NMR data, with the assistance of AI-based structure annotation tool DeepSAT. The absolute configurations of 1-3 were determined by comparing the experimental and calculated ECD spectra. Compounds 2 and 3 exhibited significant improvements in cell viability and attenuated acetaminophen-induced alanine aminotransferase levels in murine hepatocytes at 20 μM. Bioinformatics analysis and molecular docking suggested that BRAF might be a potential target for these lignans.

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Publication Details

Journal
RSC Medicinal Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5md00331h
Citations
1
Primary Topic
Drug-Induced Hepatotoxicity and Protection
Type
article
Field-Weighted Citation Impact
1.56

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article

Bioassay-guided isolation of hepatoprotective lignans from Vernonia cinerea: DeepSAT-driven structural elucidation and predictive mechanistic insights against drug-induced liver injury

Ruiying Yuan, Ming Gui, Mu Li, Meng Zhang et al.
1 citations
RSC Medicinal Chemistry
Drug-Induced Hepatotoxicity and Protection
1.56
article

Bioassay-guided isolation of hepatoprotective lignans from Vernonia cinerea: DeepSAT-driven structural elucidation and predictive mechanistic insights against drug-induced liver injury

Ruiying Yuan, Ming Gui, Mu Li, Meng Zhang, Xin Song, Jie Ping, You‐Sheng Cai, Yu-Ting Zhong
article en
1 citations

Abstract

Three new dibenzylbutane lignans, vernolignans A-C (1-3), along with three known compounds (4-6), were isolated from <i>Vernonia cinerea</i> through a bioactivity-guided isolation process. The planar structures of the new compounds (1-3) were elucidated through comprehensive analysis of HR-ESI-MS and 1D/2D NMR data, with the assistance of AI-based structure annotation tool DeepSAT. The absolute configurations of 1-3 were determined by comparing the experimental and calculated ECD spectra. Compounds 2 and 3 exhibited significant improvements in cell viability and attenuated acetaminophen-induced alanine aminotransferase levels in murine hepatocytes at 20 μM. Bioinformatics analysis and molecular docking suggested that BRAF might be a potential target for these lignans.

RSC Medicinal ChemistryVol. 16(9)
Tibet University (CN), Wuhan University (CN), Renmin Hospital of Wuhan University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Hubei Province
Openalex Percentile: Top 18%
Drug-Induced Hepatotoxicity and Protection
1.56
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