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首页> 外文期刊>Marine Drugs >Two New Tryptamine Derivatives, Leptoclinidamide and (-)-Leptoclinidamine B, from an Indonesian Ascidian Leptoclinides dubius
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Two New Tryptamine Derivatives, Leptoclinidamide and (-)-Leptoclinidamine B, from an Indonesian Ascidian Leptoclinides dubius

机译:来自印尼海鞘Leptoclinides dubius的两种新的色胺衍生物Leptoclinidamide和(-)-Leptoclinidamine B

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摘要

Two new tryptamine-derived alkaloids, named as leptoclinidamide (1) and (-)-leptoclinidamine B (2), were isolated from an Indonesian ascidian Leptoclinides dubius together with C2-α-D-mannosylpyranosyl-L-tryptophan (3). The structure of 1 was assigned on the basis of spectroscopic data for 1 and its N-acetyl derivative (4). Compound 1 was an amide of tryptamine with two β-alanine units. Although the planar structure of 2 is identical to that of the known compound (+)-leptoclinidamine B (5), compound 2 was determined to be the enantiomer of 5 based on amino acid analysis using HPLC methods. Compounds 1 to 4 were evaluated for cytotoxicity against two human cancer cell lines, HCT-15 (colon) and Jurkat (T-cell lymphoma) cells, but none of the compounds showed activity.
机译:从印尼海鞘杜比犬Leptoclinides dubius中分离出两个新的源自色胺的生物碱,分别命名为leptoclinidamide(1)和(-)-leptoclinidamine B(2),以及C 2 -α-D-甘露糖基吡喃糖基- L-色氨酸(3)。 1的结构是根据1及其N-乙酰基衍生物(4)的光谱数据指定的。化合物1是具有两个β-丙氨酸单元的色胺的酰胺。尽管2的平面结构与已知化合物(+)-瘦亚麻素B(5)的平面结构相同,但是基于使用HPLC方法的氨基酸分析,化合物2被确定为5的对映体。评估了化合物1-4对两种人类癌细胞系HCT-15(结肠)和Jurkat(T细胞淋巴瘤)细胞的细胞毒性,但这些化合物均未显示活性。

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