A new alkaloid and a new benzaldehyde derivative from the twig of Zanthoxylum rhetsa (Roxb.) DC.

被引:2
|
作者
Lookpan, Titiya [1 ,2 ,3 ]
Voravuthikunchai, Supayang P. [3 ,4 ,5 ,6 ]
Sitthisuk, Pornnapa [7 ]
Poorahong, Watcharaporn [7 ]
Watanapokasin, Ramida [7 ]
Chakthong, Suda [1 ,2 ,3 ]
机构
[1] Prince Songkla Univ, Fac Sci, Div Phys Sci, Hat Yai, Songkhla, Thailand
[2] Prince Songkla Univ, Fac Sci, Ctr Excellence Innovat Chem, Hat Yai, Songkhla, Thailand
[3] Prince Songkla Univ, Fac Sci, Nat Prod Res Ctr Excellence, Hat Yai, Songkhla, Thailand
[4] Prince Songkla Univ, Ctr Antimicrobial Biomat Innovat Southeast Asia, Hat Yai, Songkhla, Thailand
[5] Prince Songkla Univ, Fac Sci, Sci Ind Program, Hat Yai, Songkhla, Thailand
[6] Prince Songkla Univ, Fac Sci, Div Biol Sci, Hat Yai, Songkhla, Thailand
[7] Srinakharinwirot Univ, Fac Med, Dept Biochem, Bangkok, Thailand
关键词
Zanthoxylum rhetsa; alkaloid; benzaldehyde derivative; cytotoxicity; CHEMICAL-CONSTITUENTS; STEM BARK; LIMONOIDS; CHEMISTRY;
D O I
10.1080/14786419.2022.2127708
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A new alkaloid, 2-acetyl-4-methoxyfuro[2,3-b]quinoline (1), and a new benzaldehyde derivative, (2 ' S)-4-(2 '-hydroxy-3 '-methyl-3 '-butenoxy)benzaldehyde (2), were isolated from the twig of Zanthoxylum rhetsa (Roxb.) DC. along with twenty-six known compounds (3-28). Their structures were determined by spectroscopic analysis (1D and 2D NMR spectroscopy and HRMS analysis) and comparison with data reported in the literature. Thirteen of the known compounds were evaluated for their cytotoxic activities against human cancer cell lines that included MDA-MB-231, SW1353, A549, and HCT116. (+/-)-8-Acetonyldihydronitidine (15) showed moderate cytotoxicity toward the SW1353 cancer cell line with an IC50 value of 18.90 +/- 0.39 mu g/mL, and exhibited weak cytotoxic activity against MDA-MB-231, A549 and HCT116 cell lines with IC50 values of 49.86-71.32 mu g/mL.
引用
收藏
页码:463 / 469
页数:7
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