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青蒿素 U-Z:青蒿地上部分的 6 种具有抗炎活性的倍半萜。

Arteannoides U-Z: Six undescribed sesquiterpenoids with anti-inflammatory activities from the aerial parts of Artemisia annua (Qinghao).

机构信息

Institute of Traditional Chinese Medicine & Natural Products, College of Pharmacy and Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drug Research, Jinan University, Guangzhou 510632, China; Department of Ocean Science and Hong Kong Branch of Southern Marine Science and Engineering Guangdong Laboratory, the Hong Kong University of Science and Technology, Hong Kong 999077, China.

Institute of Traditional Chinese Medicine & Natural Products, College of Pharmacy and Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drug Research, Jinan University, Guangzhou 510632, China.

出版信息

Fitoterapia. 2021 Oct;154:105002. doi: 10.1016/j.fitote.2021.105002. Epub 2021 Jul 26.

Abstract

Four previously unreported sesquiterpenoid diasteromers, arteannoides U-X (1-4), together with one new norsesquiterpenoid 5 (arteannoide Y) and one undescribed rearranged cadinene sesquiterpenoid 6 (arteannoide Z) were obtained from the dried aerial parts of Artemisia annua (Qinghao). Notably, arteannoides U-X (1-4) are four stereoisomers that possess the same molecules and the same planar connectivity, but differ from each other in configuration at a certain stereocenter. Their accurate structures were unambiguously identified and distinguished by extensive spectroscopic analyses, NMR calculations with DP4+ analysis, electronic circular dichroism (ECD) calculations and X-ray diffraction analyses. Compounds 1, 3, and 4 showed inhibitory activities against the production of inflammatory cytokines (PGE, NO, IL-6 and TNF-α) in lipopolysaccharide (LPS)-induced RAW 264.7 macrophages.

摘要

从青蒿(Qinghao)的干燥地上部分中获得了四个以前未报道的倍半萜二聚体差向异构体,arteannoides U-X(1-4),以及一个新的降 nor 倍半萜 5(arteannoide Y)和一个未描述的重排卡品烯倍半萜 6(arteannoide Z)。值得注意的是,arteannoides U-X(1-4)是四个立体异构体,它们具有相同的分子和相同的平面连接,但在某个手性中心的构型上彼此不同。通过广泛的光谱分析、带有 DP4+分析的 NMR 计算、电子圆二色性(ECD)计算和 X 射线衍射分析,明确确定并区分了它们的准确结构。化合物 1、3 和 4 显示出对脂多糖(LPS)诱导的 RAW 264.7 巨噬细胞中炎症细胞因子(PGE、NO、IL-6 和 TNF-α)产生的抑制活性。

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