Lignanamides from the Roots of Metternichia macrocalyx and Their Anti-inflammatory Activity.

IF 4.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
ACS Omega Pub Date : 2024-11-13 eCollection Date: 2024-11-26 DOI:10.1021/acsomega.4c07336
Thiago Araújo de Medeiros Brito, Ana Carolina Ferreira de Albuquerque, Fernando Martins Dos Santos Junior, Paulo Bruno Araújo Loureiro, Francisco Allysson Assis Ferreira Gadelha, Marianna Vieira Sobral, Domingos Benício Oliveira Silva Cardoso, Eudes da Silva Velozo, Josean Fechine Tavares, Lucas Silva Abreu, Marcelo Sobral da Silva
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引用次数: 0

Abstract

Five new lignanamides (1-5) and ten known amides (6-15) were isolated from the chloroform extract of Metternichia macrocalyx roots. The structures of the new compounds were elucidated via analysis of NMR spectroscopic and mass spectrometry data and known structures by comparison with data from the literature. Compound 1 had its absolute configuration established through ECD experiments, NMR calculations and quantum mechanical calculations. The anti-inflammatory activity of compounds (1-5) was assessed on RAW 264.7 macrophages. All the tested compounds reduced nitric oxide levels. In the cytokine quantification assays, only compound 2 did not significantly reduce IL-10 levels. Moreover, compounds 1-3 and 5 also reduced IL-1β levels. These results suggest the anti-inflammatory potential of these compounds.

梅特尼根木质素胺类化合物及其抗炎活性研究。
从大萼美特尔根氯仿提取物中分离得到5个新的木脂素胺(1-5)和10个已知的木脂素胺(6-15)。新化合物的结构通过核磁共振谱和质谱数据的分析以及已知结构与文献数据的比较得以阐明。化合物1通过ECD实验、核磁共振计算和量子力学计算建立了绝对构型。在RAW 264.7巨噬细胞上评估化合物(1-5)的抗炎活性。所有被测试的化合物都降低了一氧化氮水平。在细胞因子定量分析中,只有化合物2没有显著降低IL-10水平。此外,化合物1-3和5也能降低IL-1β水平。这些结果表明这些化合物具有抗炎的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
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