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来源于贯叶连翘的 1,9-桥环倍半萜酰基间苯三酚

1,9-seco-Bicyclic Polyprenylated Acylphloroglucinols from Hypericum uralum.

机构信息

State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences , Kunming 650201, People's Republic of China.

University of Chinese Academy of Sciences , Beijing 100049, People's Republic of China.

出版信息

J Nat Prod. 2015 Dec 24;78(12):3075-9. doi: 10.1021/acs.jnatprod.5b00830. Epub 2015 Nov 19.

Abstract

Hyperuralones C-H (1-6), six new 1,9-seco-bicyclic polyprenylated acylphloroglucinols (1,9-seco-BPAPs) derived from the normal polyprenylated acylphloroglucinols with a bicyclo[3.3.1]nonane-2,4,9-trione core, together with six known analogues, were isolated from the aerial parts of Hypericum uralum. The structures of 1-6 were elucidated on the basis of the interpretation of NMR and MS spectroscopic data. The structure of attenuatumione B, a known compound isolated from H. attenuatum, was revised to that of a 1,9-seco-BPAP by NMR spectroscopic analysis and previous biomimetic synthesis methods. The inhibitory activities of these isolates on acetylcholinesterase were tested, and compounds 1 and 2 exhibited moderate activities with IC50 values of 9.6 and 7.1 μM, respectively.

摘要

高穗玄参 C-H(1-6),六个新的 1,9-裂环倍半萜酰基间苯三酚(1,9-seco-BPAPs),来源于具有双环[3.3.1]壬烷-2,4,9-三酮核心的正常倍半萜酰基间苯三酚,与六个已知的类似物一起,从高穗玄参的地上部分分离得到。基于 NMR 和 MS 光谱数据的解释,确定了 1-6 的结构。通过 NMR 光谱分析和以前的仿生合成方法,对从 H. attenuatum 中分离得到的已知化合物 attenuatumione B 的结构进行了修订,确定为 1,9-seco-BPAP。测试了这些分离物对乙酰胆碱酯酶的抑制活性,化合物 1 和 2 表现出中等活性,IC50 值分别为 9.6 和 7.1 μM。

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