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Piper wallichii Miq. Hand.-Mazz. 中一种新的类黄酮 C-糖苷和一种罕见的生物活性木质酰胺

A new flavonol C-glycoside and a rare bioactive lignanamide from Piper wallichii Miq. Hand.-Mazz.

机构信息

School of Pharmaceutical Sciences, Shandong University, Jinan 250012, China.

Qilu Hospital, Shandong University, Jinan 250012, China.

出版信息

Chin J Nat Med. 2014 May;12(5):377-81. doi: 10.1016/S1875-5364(14)60047-9.

Abstract

This study was conducted to investigate the chemical constituents of Piper wallichii (Miq.) Hand.-Mazz. and evaluate their biological activity. Compounds were isolated by various column chromatographic methods, and their structures were elucidated on the basis of physical characteristics and spectral data. The 1, 1-diphenyl-2-picrylhydrazyl (DPPH)-scavenging activity and acetylcholinesterase (AChE)-inhibitory activity of the compounds were evaluated. Five compounds were obtained and identified as 8-C-β-D-glucopyranosylkaempferol-3-O-β-D-glucopyranoside (1), 1, 2-dihydro-6,8-dimethoxy-7-hydroxy-1-(3, 5-dimethoxy-4-hydroxyphenyl)-N(1), N(2)-bis-[2-(4-hydroxyphenyl)ethyl]-2, 3-naphthalene dicarboxamide (2), goniothalactam (3), aristololactam A IIIa (4) and piperlonguminine (5). Compound 1 was a new flavonol C-glycoside, 2 was a rare lignanamide, which was isolated from the family Piperaceae for the first time, and compound 3 was isolated from this plant for the first time. Among them, 2 showed potent DPPH-scavenging activity, with IC50 of 31.38 ± 0.97 μmol·L(-1); Compounds 2, 3, and 4 showed AChE inhibitory activity at 100 μmol·L(-1), with inhibition rates of 28.57% ± 1.47%, 18.48% ± 2.41% and 17.4% ± 3.03%, respectively.

摘要

本研究旨在探讨胡椒(Piper wallichii(Miq.)Hand.-Mazz.)的化学成分,并评估其生物活性。采用各种柱色谱方法分离化合物,并根据物理性质和光谱数据阐明其结构。评估了化合物的 1,1-二苯基-2-苦基肼(DPPH)清除活性和乙酰胆碱酯酶(AChE)抑制活性。得到并鉴定了 5 种化合物,分别为 8-C-β-D-吡喃葡萄糖基山奈酚-3-O-β-D-吡喃葡萄糖苷(1)、1,2-二氢-6,8-二甲氧基-7-羟基-1-(3,5-二甲氧基-4-羟基苯基)-N(1),N(2)-双-[2-(4-羟基苯基)乙基]-2,3-萘二羧酸酰胺(2)、戈尼噻隆(3)、阿立洛酮 A IIIa(4)和胡椒碱(5)。化合物 1 是一种新的黄酮醇 C-糖苷,2 是一种罕见的木脂酰胺,首次从胡椒科中分离得到,化合物 3 也是首次从该植物中分离得到。其中,2 表现出较强的 DPPH 清除活性,IC50 为 31.38 ± 0.97 μmol·L(-1);化合物 2、3 和 4 在 100 μmol·L(-1)时均表现出 AChE 抑制活性,抑制率分别为 28.57% ± 1.47%、18.48% ± 2.41%和 17.4% ± 3.03%。

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