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白术根茎中倍半萜类化合物的抗炎抑制活性。

Inflammatory Inhibitory Activity of Sesquiterpenoids from Atractylodes macrocephala Rhizomes.

作者信息

Hoang Le Son, Tran Manh Hung, Lee Joo-Sang, Ngo Quynh Mai Thi, Woo Mi Hee, Min Byung Sun

机构信息

College of Pharmacy, Drug Research and Development Center, Catholic University of Daegu.

出版信息

Chem Pharm Bull (Tokyo). 2016;64(5):507-11. doi: 10.1248/cpb.c15-00805.

Abstract

Three new sesquiterpenoids, 13-hydroxyl-atractylenolide II (1), 4-ketone-atractylenolide III (2), and eudesm-4(15)-ene-7β,11-diol (3), along with eleven known compounds (4-14), were isolated from the rhizomes of Atractylodes macrocephala. The structures and relative configurations of 1-3 were determined by analysis of the spectroscopic data, and the absolute configurations of 1 and 2 were assigned by circular dichroism technique. The anti-inflammatory activities of these isolates were evaluated against lipopolysaccharide-induced nitric oxide production in macrophage RAW264.7 cells; compounds 4, 7, and 8 exhibited moderate efficacy with IC50 values of 48.6±0.5, 46.4±3.2, and 32.3±2.9 µM, respectively.

摘要

从白术根茎中分离出三种新的倍半萜类化合物,13-羟基苍术内酯II(1)、4-酮基苍术内酯III(2)和桉叶-4(15)-烯-7β,11-二醇(3),以及十一种已知化合物(4-14)。通过光谱数据分析确定了1-3的结构和相对构型,并采用圆二色技术确定了1和2的绝对构型。评估了这些分离物对巨噬细胞RAW264.7中脂多糖诱导的一氧化氮产生的抗炎活性;化合物4、7和8表现出中等效力,IC50值分别为48.6±0.5、46.4±3.2和32.3±2.9μM。

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