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从贯叶连翘中分离得到的 9 个具有潜在抗抑郁和保肝活性的prenylated acylphloroglucinols。

Nine prenylated acylphloroglucinols with potential anti-depressive and hepatoprotective activities from Hypericum scabrum.

机构信息

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, People's Republic of China.

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, People's Republic of China.

出版信息

Bioorg Chem. 2021 Feb;107:104529. doi: 10.1016/j.bioorg.2020.104529. Epub 2020 Dec 3.

Abstract

In our screening program for new biologically active secondary metabolites, nine new polycyclic polyprenyled acylphloroglucinols, hyperscabins D-L, together with three known compounds, were obtained from the aerial parts of Hypericum scabrum. The chemical structures of 1-9 were characterized by extensive spectroscopic analyses, nuclear magnetic resonance calculation with DP4+ probability analysis, and the electronic circular dichroism spectra were calculated. Compound 1 was an unusual prenylated acylphloroglucinol decorated with a 5-oxaspiro [4,5] deca-1,9-dione skeleton. Compound 2 was a newly identified spirocyclic polyprenylated acylphloroglucinol possessing a rare 5,5-spiroketal segment. Compounds 3, 8, and 10 (10 μM) exhibited pronounced hepatoprotective activity against d-galactosamine-induced WB-F344 cell damage in vitro assays. All test compounds (1, 3, and 7-12) demonstrated potential inhibitory effects at 10 μM against noradrenalinet ([H]-NE) reuptake in rat brain synaptosome.

摘要

在我们的新型生物活性次生代谢产物的筛选计划中,从贯叶连翘的地上部分分离得到了 9 个新的多环多聚异戊烯酰基间苯三酚,分别命名为 hyperscabins D-L,同时还分离得到了 3 个已知化合物。通过广泛的光谱分析、基于 DP4+概率分析的核磁共振计算和电子圆二色光谱计算,确定了化合物 1-9 的化学结构。化合物 1 是一个具有 5-氧杂螺[4.5]癸-1,9-二酮骨架的罕见异戊烯酰基间苯三酚。化合物 2 是一个新鉴定的具有罕见 5,5-螺缩酮片段的环状多聚异戊烯酰基间苯三酚。化合物 3、8 和 10(10 μM)在体外试验中对 D-半乳糖胺诱导的 WB-F344 细胞损伤表现出显著的肝保护活性。所有测试化合物(1、3 和 7-12)在 10 μM 时均表现出对大鼠脑突触体去甲肾上腺素([H]-NE)再摄取的潜在抑制作用。

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