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在新型萘醌化合物中寻找针对细菌生物膜的潜在抗菌先导结构。

Searching for a potential antibacterial lead structure against bacterial biofilms among new naphthoquinone compounds.

作者信息

Moreira C S, Silva A C J A, Novais J S, Sá Figueiredo A M, Ferreira V F, da Rocha D R, Castro H C

机构信息

Organic Chemistry Department, Chemistry Institute, Federal Fluminense University, Niterói, Rio de Janeiro, Brazil.

Molecular and Cell Biology Department, PPBI, Biology Institute, Federal Fluminense University, Niterói, Rio de Janeiro, Brazil.

出版信息

J Appl Microbiol. 2017 Mar;122(3):651-662. doi: 10.1111/jam.13369. Epub 2017 Jan 25.

Abstract

AIMS

The aims of this study were to design, synthesize and to evaluate 2-hydroxy-3-phenylsulfanylmethyl-[1,4]-naphthoquinones against Gram-negative and Gram-positive bacterial strains, including methicillin-resistant Staphylococcus aureus (MRSA) and its biofilm, to probe for potential lead structures.

METHODS AND RESULTS

Thirty-six new analogues were prepared with good yields using a simple, fast, operational three-procedure reaction and a thiol addition to an ο-quinone methide using microwave irradiation. All compounds were tested against Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, Proteus mirabilis ATCC 15290, Serratia marcescens ATCC 14756, Klebsiella pneumoniae ATCC 4352, Enterobacter cloacae ATCC 23355, Enterococcus faecalis ATCC 29212, S. aureus ATCC 25923, Staphylococcus simulans ATCC 27851, Staphylococcus epidermidis ATCC 12228 and a hospital strain of MRSA. Their antibacterial activity was determined using the disc diffusion method, revealing the activity of 19 compounds, mainly against Gram-positive strains. Interestingly, the minimal inhibitory concentration ranges detected for the hit molecules (32-128 μg ml ) were within Clinical and Laboratory Standards Institute levels. Promisingly, compound 15 affected the MRSA strain, with a reduction of up to 50% in biofilm formation, which is better than vancomycin as biofilm forms a barrier against the antibiotic that avoids its action.

CONCLUSIONS

After probing 36 naphthoquinones for a potential antibacterial lead structure against the bacterial biofilm, we found that compound 15 should be explored further and also should be structurally modified in the near future to test against Gram-negative strains.

SIGNIFICANCE AND IMPACT OF THE STUDY

Since vancomycin is one of the last treatment options currently available, and it is unable to inhibit biofilm, the research of new antimicrobials is urgent. In this context, 2-hydroxy-3-phenylsulfanylmethyl-[1,4]-naphthoquinones proved to be a promising lead structure against MRSA and bacterial biofilm.

摘要

目的

本研究旨在设计、合成并评估2-羟基-3-苯硫基甲基-[1,4]-萘醌对革兰氏阴性菌和革兰氏阳性菌菌株的抗菌活性,包括耐甲氧西林金黄色葡萄球菌(MRSA)及其生物膜,以探寻潜在的先导结构。

方法与结果

使用简单、快速、可操作的三步反应,并通过微波辐射使硫醇加成到邻醌甲基化物上,以良好的产率制备了36种新类似物。所有化合物均针对大肠杆菌ATCC 25922、铜绿假单胞菌ATCC 27853、奇异变形杆菌ATCC 15290、粘质沙雷氏菌ATCC 14756、肺炎克雷伯菌ATCC 4352、阴沟肠杆菌ATCC 23355、粪肠球菌ATCC 29212、金黄色葡萄球菌ATCC 25923、模仿葡萄球菌ATCC 27851、表皮葡萄球菌ATCC 12228以及一株医院分离的MRSA进行了测试。采用纸片扩散法测定其抗菌活性,结果显示19种化合物具有活性,主要针对革兰氏阳性菌菌株。有趣的是,对活性分子检测到的最低抑菌浓度范围(32 - 128μg/ml)处于临床和实验室标准协会规定的水平内。有前景的是,化合物15对MRSA菌株有影响,生物膜形成减少高达50%,这比万古霉素更好,因为生物膜会形成一道屏障阻碍抗生素发挥作用。

结论

在探究36种萘醌针对细菌生物膜的潜在抗菌先导结构后,我们发现化合物15应进一步深入研究,并且在不久的将来应对其进行结构修饰以测试对革兰氏阴性菌菌株的抗菌活性。

研究的意义与影响

由于万古霉素是目前可用的最后治疗选择之一,且它无法抑制生物膜,因此新型抗菌药物的研究迫在眉睫。在此背景下,2-羟基-3-苯硫基甲基-[启1,4]-萘醌被证明是针对MRSA和细菌生物膜的一种有前景的先导结构。

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