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来自滇金丝桃的多环多异戊烯基酰基间苯三酚及其保肝活性。

Polycyclic polyprenylated acylphloroglucinols from Hypericum beanii and their hepatoprotective activity.

作者信息

Ma Yonghui, Suo Xinyue, Li Xiaoxiu, Zhu Tingting, Li Jin, Ji Tengfei, Liu Bo

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; The Key Laboratory of Plant Stress Biology in Arid Land, College of Life Sciences, Xinjiang Normal University, Ürümqi, Xinjiang, 830054, 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

Phytochemistry. 2022 Nov;203:113413. doi: 10.1016/j.phytochem.2022.113413. Epub 2022 Aug 28.

Abstract

Twenty-seven polycyclic polyprenylated acylphloroglucinols (PPAPs) with diverse skeletons, including seven previously undescribed ones (hyperbeanins A-G), were isolated from the aerial parts of Hypericum beanii. Their structures were established by comprehensive analysis of NMR, HRESIMS, and experimental electronic circular dichroism (ECD) spectra. Hyperbeanin A was a monocyclic polyprenylated acylphloroglucinols (MPAPs) with an unusual spiro-fused cyclopropane ring. Four of the isolated compounds showed obvious hepatoprotective activity against paracetamol-induced HepG2 cell damage at 10 μM. The present results suggested that these compounds would be potential hepatoprotective agents. In addition, the plausible biogenetic pathways of hyperbeanins A-G were proposed, which gave an insight for future biomimetic synthesis of them.

摘要

从赶山鞭的地上部分分离出27种具有不同骨架的多环多异戊烯基酰基间苯三酚(PPAPs),其中包括7种以前未描述过的化合物(赶山鞭素A - G)。通过对核磁共振(NMR)、高分辨电喷雾电离质谱(HRESIMS)和实验性电子圆二色光谱(ECD)的综合分析确定了它们的结构。赶山鞭素A是一种具有不寻常螺环稠合环丙烷环的单环多异戊烯基酰基间苯三酚(MPAPs)。其中4种分离出的化合物在10 μM浓度下对扑热息痛诱导的HepG2细胞损伤表现出明显的肝保护活性。目前的结果表明这些化合物可能是潜在的肝保护剂。此外,还提出了赶山鞭素A - G可能的生物合成途径,这为它们未来的仿生合成提供了思路。

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