Novel rearranged acetophenone derivatives possessing diverse architectures from the leaves of Melicope ptelefolia |
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Authors: | Jin-Fang Xu Chao Han Gui-Min Xue Xiao-Bing Wang Jun Luo Ming-Hua Yang Jian-Guang Luo Ling-Yi Kong |
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Affiliation: | 1. Jiangsu Key Laboratory of Bioactive Natural Product Research and State Key Laboratory of Natural Medicines, School of Traditional Chinese Pharmacy, China Pharmaceutical University, 24 Tong Jia Xiang, Nanjing 210009, People’s Republic of China;2. School of Pharmaceutical Science, Shanxi Medical University, 56 Xinjian Road, Taiyuan 030001, People’s Republic of China |
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Abstract: | Melicolones C–K (1–9), nine acetophenone derivatives with three unprecedented architectures, were characterized from the leaves of Melicope ptelefolia. Among them, melicolone C (1) was a novel acetophenone analogue possessing a highly rearranged spiro skeleton. Melicolones D-F (2–4) were three novel acetophenone congeners bearing unusual octalactone ring. Melicolones G-K (5–9) were five new prenylated acetophenone derivatives featuring a 9-oxatricyclo [3.2.1.13, 8]nonane core. Their structures were established by extensive spectroscopic analysis and ECD spectra. These different structures were presumably derived from the same precursor via three major biosynthetic pathways. Compounds 5–9 exerted moderate effects to reverse multidrug-resistance in MCF-7/ADR cells with reversal fold values ranging from 6.2 to 13.3. |
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Keywords: | Corresponding author. Acetophenone derivatives Rearrangement Multidrug resistance Natural products |
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