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枝珊瑚酸 A 和 B:一种来自 sp. 海洋海绵的含氮、重排海绵诺二萜

Dendrillic Acids A and B: Nitrogenous, Rearranged Spongian Nor-Diterpenes from a sp. Marine Sponge.

机构信息

School of Molecular Sciences, The University of Western Australia, Crawley, WA 6009, Australia.

Australian National Phenome Centre and Centre for Computational and Systems Medicine, Health Futures Institute, Murdoch University, Harry Perkins Building, Perth, WA 6150, Australia.

出版信息

J Nat Prod. 2023 Mar 24;86(3):482-489. doi: 10.1021/acs.jnatprod.2c01087. Epub 2023 Mar 16.

Abstract

Two nitrogenous rearranged spongian nor-diterpenoids, dendrillic acids A and B, were isolated from a marine sponge sp. (order: Dendroceratida; family: Darwinellidae). The structures of the metabolites were elucidated on the basis of spectroscopic analysis as well as density functional theory prediction of NMR chemical shifts and application of the DP4+ algorithm. The absolute configuration of the metabolites was established via comparison of experimental and time-dependent density functional theory predicted electronic circular dichroism data. An unusual epimerization reaction was observed leading to the interconversion of the metabolites upon storage in dimethyl sulfoxide solution, which is proposed to proceed via an anionic pathway as probed via isotopic incorporation experiments. Evaluation against a panel of micro-organisms and cell lines revealed that the compounds were devoid of any significant biological activity against all organisms tested, with the exception of mild antiprotozoal activity displayed by dendrillic acid B () against .

摘要

从海洋海绵 sp.(目:Dendroceratida;科:Darwinellidae)中分离得到两种氮杂重排海绵二萜类化合物 dendrillic 酸 A 和 B。根据光谱分析以及 NMR 化学位移的密度泛函理论预测和 DP4+算法的应用,确定了代谢物的结构。通过比较实验和时间依赖的密度泛函理论预测的电子圆二色性数据,确定了代谢物的绝对构型。在二甲基亚砜溶液中储存时,观察到一种不寻常的差向异构化反应,导致代谢物的相互转化,该反应被提出通过同位素掺入实验探测到的阴离子途径进行。对一系列微生物和细胞系的评估表明,除了 dendrillic 酸 B ()对 显示出轻微的抗原生动物活性外,这些化合物对所有测试的生物均没有任何显著的生物活性。

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