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Novel quinolinone alkaloids bearing a lignoid moiety and related constituents in the leaves of Melicope denhamii

机译:新型的喹啉酮生物碱,在木蒜的叶子中带有木质素部分和相关成分

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摘要

Six novel quinolinone alkaloids bearing a phenylpropanoid or a coumarin moiety, named melicodenines C-H (1-6), two new cinnamyl alcohol derivatives, named melicodins A (7) and B (8), and a new coumarinolignan, named melicodin C (9), were isolated from the leaves of Melicope denhamii (Seem.) T. G. Hartley. Their structures were established by spectroscopic analyses including extensive 2D-NMR experiments. Compounds 1-5 and 9 possess a cyclobutane ring and are hypothetically produced by a [2+2] cycloaddition, whereas compound 6 is presumed to form through a Diels-Alder cycloaddition followed by the elimination of an acetone molecule. Ten quinolinone alkaloids (1-6, 10-13) and a coumarinolignan (9) were tested for anti-proliferative activity against DLD-1 human colon cancer cells. Melicodenine G (5) showed the most potent inhibitory activity, causing the induction of apoptosis with an IC _(50) value of 9.4±0.3 μM.
机译:六种带有苯基丙烷或香豆素部分的新型喹啉酮生物碱,名为melicodenines CH(1-6),两种新的肉桂醇衍生物,分别命名为三叶菊甲素A(7)和B(8),以及一种新的香豆素,其命名为melicodin C(9)从Melicope denhamii(Seem。)TG Hartley的叶子中分离得到。通过光谱分析,包括广泛的2D-NMR实验,确定了它们的结构。化合物1-5和9具有环丁烷环,并且假设是通过[2 + 2]环加成反应生成的,而推测化合物6是通过Diels-Alder环加成反应形成的,然后消除了丙酮分子。测试了十种喹啉酮生物碱(1-6、10-13)和香豆素(9)对DLD-1人结肠癌细胞的抗增殖活性。 Melicodenine G(5)表现出最强的抑制活性,引起凋亡诱导,IC _(50)值为9.4±0.3μM。

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