Antibacterial Potential of a New Endiandric Acid From Beilschmiedia acuta (Lauraceae) Against Drug-resistant Bacteria.

IF 2.3 3区 化学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Guy Raphael Sado Nouemsi, Olive Monique Fotso Demgne, Peron Bosco Leutcha, François Damen, James Deke Simo Mpetga, İlhami Çelik, Mathieu Téné, Victor Kuete, Alain Meli Lannang
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引用次数: 0

Abstract

A previously unidentified endiandric acid derivative named beilschmiedic acid P (1), together with eight (2-9) known compounds including four pentacyclic triterpenoids (3-6), one amide (2) and, three steroids (7-9) were isolated from Beilschmiedia acuta stem barks. Chromatographic techniques were used for these isolations while their characterization was based on their one-/two-dimensional nuclear magnetic resonance and mass spectrometry experiments. The antibacterial activity of the new compound (1) was tested via INT colourimetric assay against nine bacterial strains all expressing multidrug-resistant phenotypes including Klebsiella pneumoniae (KP55), Escherichia coli (AG102 and ATCC8739), Pseudomonas aeruginosa (PA124 and PA01), Enterobacter aerogenes (EA27 and ATCC13048) and Providencia stuartii (PS2636 and ATCC29916). The activity was categorised based on the scale described by Kuete (2010), as significantly active for minimal inhibitory concentration (MIC) ≤ 10 µg/mL, moderately active for 10 µg/mL < MIC ≤ 100 µg/mL and weakly active for MIC > 100 µg/mL. The results showed a moderately active antibacterial activity of compound 1 at a rate of 77.78% (7/9) on the tested strains that is, seven out of the nine bacteria were sensitive to the action of the tested compound. Among the tested strains, E. coli (ATCC8739) showed the most efficient MIC value of 16 µg/mL.

一种新的樟科植物尖头藤酸对耐药细菌的抑菌活性研究。
从北花茎皮中分离得到了一个未被鉴定的端花酸衍生物beilschmiedic acid P(1)和8个已知化合物,包括4个五环三萜(3-6)、1个酰胺(2)和3个甾体(7-9)。这些分离物采用色谱技术,而它们的特性是基于它们的一/二维核磁共振和质谱实验。采用INT比色法对肺炎克雷伯菌(KP55)、大肠杆菌(AG102和ATCC8739)、铜绿假单胞菌(PA124和PA01)、产气肠杆菌(EA27和ATCC13048)和斯图尔普罗维顿菌(PS2636和ATCC29916)等9株多药耐药菌株进行了抑菌活性检测。根据Kuete(2010)描述的尺度,将活性分类为最小抑制浓度(MIC)≤10 μ g/mL时显着活性,10 μ g/mL < MIC≤100 μ g/mL时中度活性,MIC bb0 100 μ g/mL时弱活性。结果表明,化合物1对被试菌株的抑菌活性为77.78%(7/9),即9株细菌中有7株对化合物的作用敏感。其中大肠杆菌(ATCC8739)的MIC值最高,为16µg/mL。
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
Chemistry & Biodiversity
Chemistry & Biodiversity 环境科学-化学综合
CiteScore
3.40
自引率
10.30%
发文量
475
审稿时长
2.6 months
期刊介绍: Chemistry & Biodiversity serves as a high-quality publishing forum covering a wide range of biorelevant topics for a truly international audience. This journal publishes both field-specific and interdisciplinary contributions on all aspects of biologically relevant chemistry research in the form of full-length original papers, short communications, invited reviews, and commentaries. It covers all research fields straddling the border between the chemical and biological sciences, with the ultimate goal of broadening our understanding of how nature works at a molecular level. Since 2017, Chemistry & Biodiversity is published in an online-only format.
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