Toonamonoids A and B: two new limonoids from <i>Toona ciliata</i> var <i>. yunnanensis</i> (C.DC.) C.Y.Wu and their cytotoxic activity

Two previously undescribed limonoids, designated as toonamonoids A and B (<b>1-2</b>), featuring a rare <i>γ</i>-crotonolactone motif at C-17 instead of the typical furan ring, were isolated from <i>Toona ciliata.</i> var<i>. yunnanensis</i> (C.DC.) C.Y.Wu. Along with these, three known analogues (<b>3-5</b>) were also identified. The compounds were extracted using ethyl acetate (EtOAc) from the plant's twigs and leaves. Structural elucidation, including determination of absolute stereochemistry, was accomplished through comprehensive spectroscopic analysis involving 1D and 2D NMR techniques, complemented by high-resolution mass spectrometry (HRMS). <i>In vitro</i> cytotoxicity was assessed against two human cancer cell lines. However, none of the isolated compounds (IC<sub>50</sub> values >10 <i>μ</i>M) demonstrated notable cytotoxic activity when compared to the cisplatin.

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Publication Details

Journal
Natural Product Research
Published
2025-12-11
DOI
https://doi.org/10.1080/14786419.2025.2598829
Primary Topic
Phytochemical compounds biological activities
Type
article
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article

Toonamonoids A and B: two new limonoids from Toona ciliata var . yunnanensis (C.DC.) C.Y.Wu and their cytotoxic activity

Xiaoqin Yang, Weihua Wang, Sida Xie, Mingwang Luo et al.
Natural Product Research
Phytochemical compounds biological activities
article

Toonamonoids A and B: two new limonoids from Toona ciliata var . yunnanensis (C.DC.) C.Y.Wu and their cytotoxic activity

Xiaoqin Yang, Weihua Wang, Sida Xie, Mingwang Luo, Qiangxin Zhang, Guolei Zhu, Shengyun Wei, Yujie Li, Lu Li, Ping Zhao, Wei Yang
article en

Abstract

Two previously undescribed limonoids, designated as toonamonoids A and B (<b>1-2</b>), featuring a rare <i>γ</i>-crotonolactone motif at C-17 instead of the typical furan ring, were isolated from <i>Toona ciliata.</i> var<i>. yunnanensis</i> (C.DC.) C.Y.Wu. Along with these, three known analogues (<b>3-5</b>) were also identified. The compounds were extracted using ethyl acetate (EtOAc) from the plant's twigs and leaves. Structural elucidation, including determination of absolute stereochemistry, was accomplished through comprehensive spectroscopic analysis involving 1D and 2D NMR techniques, complemented by high-resolution mass spectrometry (HRMS). <i>In vitro</i> cytotoxicity was assessed against two human cancer cell lines. However, none of the isolated compounds (IC<sub>50</sub> values >10 <i>μ</i>M) demonstrated notable cytotoxic activity when compared to the cisplatin.

Natural Product Research
Southwest Forestry University (CN), Zhaotong University (CN), State Forestry and Grassland Administration (CN)
Openalex Percentile: Top 64%
Phytochemical compounds biological activities
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Toonamonoids A and B: two new limonoids from <i>Toona ciliata</i> var <i>. yunnanensis</i> (C.DC.) C.Y.Wu and their cytotoxic activity — Xiaoqin Yang, Weihua Wang, et al. · Natural Product Research (2025) | TGRS Research Map | TGRS