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节旋藻 A 和 B,两种来自绿藻节旋藻的新型双吲哚生物碱。

Racemosins A and B, two novel bisindole alkaloids from the green alga Caulerpa racemosa.

机构信息

School of Pharmacy, Nanchang University, 461 Bayi Road, Nanchang 330006, PR China.

School of Pharmacy, Nanchang University, 461 Bayi Road, Nanchang 330006, PR China; Institute of Translational Medicine, Nanchang University, Nanchang 330031, PR China.

出版信息

Fitoterapia. 2013 Dec;91:15-20. doi: 10.1016/j.fitote.2013.08.014. Epub 2013 Aug 24.

Abstract

Racemosin A (1), a structurally unique bisindole alkaloid possessing the seco-indolo[3,2-a]carbazole skeleton with two uncommon indolinenone units both conjugated with a methyl propenoate moiety, and its unusual cyclized derivative, racemosin B (2), were isolated from the green alga Caulerpa racemosa, together with the most commonly encountered pigment in the genus Caulerpa, caulerpin (3). Their structures were elucidated by extensive spectroscopic analysis and by comparison with data for related known compounds. A plausible biosynthetic pathway of 1 and 2 was proposed. In a neuro-protective assay, compound 1 significantly attenuated the Aβ2(5-35)-induced SH-SY5Y cell damage with a 14.6% increase in cell viability at the concentration of 10μM when compared to epigallocatechin gallate (EGCG, 16.57% increase at 10 μM) as the positive control.

摘要

从绿藻角果藻中分离得到了结构独特的双吲哚生物碱 racemosin A(1),其具有 seco-indolo[3,2-a]咔唑骨架,两个不常见的吲哚啉酮单元均与一个甲基丙烯酰基部分共轭,以及其不常见的环化衍生物 racemosin B(2),同时还分离得到了该属中最常见的色素角叉菜素(3)。通过广泛的光谱分析并与相关已知化合物的数据进行比较,确定了它们的结构。提出了 1 和 2 的可能生物合成途径。在神经保护测定中,与阳性对照表没食子儿茶素没食子酸酯(EGCG,在 10μM 时增加 16.57%)相比,化合物 1 在 10μM 浓度下可使 Aβ2(5-35)诱导的 SH-SY5Y 细胞损伤显著减弱,细胞活力增加 14.6%。

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