Phytochemistry2022,Vol.20011.DOI:10.1016/j.phytochem.2022.113186

Cipacinerasins A–K, structurally diverse limonoids from Cipadessa baccifera

Liu H.-F. Ni zhang Li J.-Y. Pan W.-D. Deng C.-Y. Lou H.-Y. Chen C. Zhang D.-Y.
Phytochemistry2022,Vol.20011.DOI:10.1016/j.phytochem.2022.113186

Cipacinerasins A–K, structurally diverse limonoids from Cipadessa baccifera

Liu H.-F. 1Ni zhang 1Li J.-Y. 1Pan W.-D. 1Deng C.-Y. 2Lou H.-Y. 1Chen C. 1Zhang D.-Y.1
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作者信息

  • 1. State Key Laboratory of Functions and Applications of Medicinal Plants Guizhou Medical University
  • 2. Qianxinan Karst Regional Development Institute of Guizhou
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Abstract

? 2022 Elsevier LtdEleven undescribed limonoids, cipacinerasins A–K, involving of four diverse carbon skeletal types, along with fifteen known analogues, were isolated from the branches and leaves of Cipadessa baccifera. Within them, cipacinerasins A and B feature a rearranged tetrahydropyranyl ring B formed between C-8 and C-30, are unusual miscellaneous-type limonoids. Cipacinerasins E and F are rare trijugin-type limonoids, of which the D-ring δ-lactone is cleaved. Their structures were elucidated on the basis of extensive spectroscopic data (HRESIMS, NMR, UV and IR), electronic circular dichroism (ECD) calculations, and single-crystal X-ray diffraction analysis. All compounds were evaluated in vitro cytotoxicity against five human tumor cell lines (K562, HeLa, PC3, LN-Cap and Hell), and cipacinerasin E showed moderate antitumor activity with IC50 values ranging from 8.0 to 24.8 μM.

Key words

Antineoplastic activity/Cipacinerasin/Cipadessa baccifera/Limonoids/Meliaceae

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出版年

2022
Phytochemistry

Phytochemistry

CCR
ISSN:0031-9422
被引量3
参考文献量24
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