Two undescribed biphenyl cyclooctene lignans with anti-inflammatory and anti-oxidant activities from the fruits of <i>Schisandra grandiflora</i>

Two undescribed biphenyl cyclooctene lignans, Schisandrin H (<b>1</b>) and Schisandrin S (<b>2</b>), and two known compounds (<b>3</b>) and (<b>4</b>), were extracted from fruits of <i>Schisandra grandiflora</i>. Structural elucidation was achieved through integrated UV, HRESIMS, NMR, ECD and ORD data analysis. At 1 μmol/L, inhibition of LPS-induced NO production in RAW264.7 macrophages was 28.85 ± 4.60% (compound <b>2</b>), 8.36 ± 5.33% (<b>3</b>), 16.72 ± 4.42% (<b>4</b>) and 38.25 ± 2.54% for dexamethasone (positive control), relative to the model group. Additionally, all compounds were evaluated for <i>in vitro</i> anti-oxidant activity using DPPH and ABTS<sup>+</sup> radical scavenging methods. Compounds <b>2</b> and <b>4</b> showed appreciable ABTS<sup>+</sup> scavenging activity, with activity levels comparable to VC at higher concentrations.

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Publication Details

Journal
Natural Product Research
Published
2026-01-20
DOI
https://doi.org/10.1080/14786419.2026.2614405
Primary Topic
Plant-derived Lignans Synthesis and Bioactivity
Type
article
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article

Two undescribed biphenyl cyclooctene lignans with anti-inflammatory and anti-oxidant activities from the fruits of Schisandra grandiflora

Chenglong Yin, Yongcheng Yang, Yongguo Li, Conglong Xia et al.
Natural Product Research
Plant-derived Lignans Synthesis and Bioactivity
article

Two undescribed biphenyl cyclooctene lignans with anti-inflammatory and anti-oxidant activities from the fruits of Schisandra grandiflora

Chenglong Yin, Yongcheng Yang, Yongguo Li, Conglong Xia, Yan Yang, Jian Li, Ziqiao Xu
article en

Abstract

Two undescribed biphenyl cyclooctene lignans, Schisandrin H (<b>1</b>) and Schisandrin S (<b>2</b>), and two known compounds (<b>3</b>) and (<b>4</b>), were extracted from fruits of <i>Schisandra grandiflora</i>. Structural elucidation was achieved through integrated UV, HRESIMS, NMR, ECD and ORD data analysis. At 1 μmol/L, inhibition of LPS-induced NO production in RAW264.7 macrophages was 28.85 ± 4.60% (compound <b>2</b>), 8.36 ± 5.33% (<b>3</b>), 16.72 ± 4.42% (<b>4</b>) and 38.25 ± 2.54% for dexamethasone (positive control), relative to the model group. Additionally, all compounds were evaluated for <i>in vitro</i> anti-oxidant activity using DPPH and ABTS<sup>+</sup> radical scavenging methods. Compounds <b>2</b> and <b>4</b> showed appreciable ABTS<sup>+</sup> scavenging activity, with activity levels comparable to VC at higher concentrations.

Natural Product Research
Yunnan Machinery Research and Design Institute (CN), Dali University (CN)
Openalex Percentile: Top 84%
Plant-derived Lignans Synthesis and Bioactivity
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