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乔治亚冷杉的单萜和倍半萜、类黄酮、木脂素和其他杂类化合物。

Mono- and sesquiterpenoids, flavonoids, lignans, and other miscellaneous compounds of Abies georgei.

机构信息

Department of Natural Product Chemistry, School of Pharmacy, Second Military University, Shanghai, China.

出版信息

Planta Med. 2011 May;77(7):742-8. doi: 10.1055/s-0030-1250550. Epub 2010 Nov 23.

Abstract

A systematic phytochemical investigation of the aerial parts of Abies georgei yielded nine new and 72 known compounds, including four monoterpenes, four sesquiterpenes, 25 flavonones, 14 lignans, and 34 other chemical constituents. The new compounds included two monoterpenes (1 and 2), two sesquiterpenes (3 and 4), three flavonones (5, 6, and 7), and two other components (8 and 9). Their chemical structures were established on the basis of various spectroscopic data. All the isolates were tested for antitumor and anti-inflammatory activities. The new compound 9,4'-dihydroxy-5,7-dimethoxy-8-methylchalcone (7) demonstrated a moderate antiproliferative effect on QGY-7703 tumor cells (IC (50)  = 17.6 µg/mL). The known compound isoferulaldehyde (67) exhibited the strongest inhibitory activity against lipopolysaccharide (LPS)-induced NO production in RAW 264.7 macrophages (IC (50) = 19.0 µg/mL). Abies georgei may be a significant source of beneficial pharmaceutical compounds.

摘要

对乔治冷杉的地上部分进行系统的植物化学研究,得到了 9 个新化合物和 72 个已知化合物,包括 4 个单萜、4 个倍半萜、25 个黄酮类化合物、14 个木脂素和 34 个其他化学成分。新化合物包括 2 个单萜(1 和 2)、2 个倍半萜(3 和 4)、3 个黄酮(5、6 和 7)和 2 个其他成分(8 和 9)。它们的化学结构是基于各种光谱数据确定的。所有分离物均进行了抗肿瘤和抗炎活性测试。新化合物 9,4'-二羟基-5,7-二甲氧基-8-甲基查尔酮(7)对 QGY-7703 肿瘤细胞表现出中等的增殖抑制作用(IC(50)= 17.6 µg/mL)。已知化合物异阿魏醛(67)对 RAW 264.7 巨噬细胞中脂多糖(LPS)诱导的 NO 产生表现出最强的抑制活性(IC(50)= 19.0 µg/mL)。乔治冷杉可能是有益药物化合物的重要来源。

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