4.4 Article

Three quinolinone alkaloid - phenylpropanoid adducts from Melicope pteleifolia

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NATURAL PRODUCT RESEARCH
卷 36, 期 15, 页码 3858-3864

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TAYLOR & FRANCIS LTD
DOI: 10.1080/14786419.2021.1892669

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Melicope pteleifolia; quinolinone alkaloid  −   phenylpropanoid derivative; melicoptines A  −   C; cytotoxic activities

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The preliminary cytotoxic test on extracts of Melicope pteleifolia collected in Dak Nong province, Vietnam showed that the n-hexane extract was the most potent. Six compounds were isolated from the n-hexane extract, including three new quinolinone alkaloid-phenylpropanoid derivatives and three known compounds. These compounds were evaluated for their anti-bacterial and cytotoxic activities against various cancer cell lines and normal fibroblasts, but all showed no activity.
Preliminary in vitro cytotoxic test on different extracts of Melicope pteleifolia collected at Dak Nong province, Vietnam showed that the n-hexane one was the most potent. From this n-hexane extract, three new quinolinone alkaloid-phenylpropanoid derivatives (1-3) and three known compounds (4-6) were isolated. Based on NMR and HR-MS analysis, their chemical structures were elucidated as melicoptines A-C (1-3), flindersine (4), 3,4,5-trimethoxybenzoic acid (5) and (24S)-methylcholestan-1 alpha,3 beta-diol (6). Isolated compounds (1-4) were evaluated for their anti-bacterial and cytotoxic activities against human non-small cell lung cancer (A549), human cervical cancer (HeLa), human Burkitt's lymphoma (Raji) and normal fibroblasts (NIH-3T3). All of them were inactive.

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