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合成新型百里香酚衍生物以对抗耐甲氧西林金黄色葡萄球菌和产超广谱β-内酰胺酶的病原菌。

Synthesis of novel thymol derivatives against MRSA and ESBL producing pathogenic bacteria.

机构信息

Central Research Laboratory, IMS and Sum Hospital, Siksha 'O' Anusandhan (Deemed to be University) , Bhubaneswar , India.

Department of Pharmaceutical Chemistry, School of Pharmaceutical Sciences, Siksha 'O' Anusandhan (Deemed to be University) , Bhubaneswar , India.

出版信息

Nat Prod Res. 2019 Nov;33(22):3181-3189. doi: 10.1080/14786419.2018.1474465. Epub 2018 May 24.

Abstract

Twelve substituted aryl-azo-thymol derivatives ( to ) were synthesized and characterized by several spectral techniques such as, FTIR, UV-vis, proton NMR, Mass spectrometry and elemental analysis. Antimicrobial activities were evaluated by agar-well diffusion method against isolated MRSA, ESBL-producing pathogenic bacteria and antifungal resistant fungi, . In addition, drug likeness properties of derivatives were assessed through bioinformatic tools such as, PASS prediction, molecular docking and Lipinski rules of five, along with determination of toxic nature and LD values. Among 12 derivatives, , , , and had significant antibacterial and antifungal activities with minimum inhibitory concentration values, 40 to 80 μg/ml. Moreover, the docking scores of derivatives were -8.27 to -11.44 kcal/mol, against 4 bacterial targets and -9.45 to -12.49 kcal/mol against 2 fungal targets. Thus, from and studies, thymol derivatives had control of MRSA, ESBL-producing bacteria and antifungal resistant fungi.

摘要

合成了 12 种取代芳基偶氮噻吨酮衍生物(to),并通过傅里叶变换红外光谱(FTIR)、紫外可见光谱(UV-vis)、质子核磁共振(1H NMR)、质谱(MS)和元素分析等多种光谱技术对其进行了表征。采用琼脂孔扩散法对分离出的耐甲氧西林金黄色葡萄球菌(MRSA)、产超广谱β-内酰胺酶(ESBL)的病原菌和抗真菌耐药真菌进行了抗菌活性评价。此外,还通过 PASS 预测、分子对接和 Lipinski 五规则等生物信息学工具,以及毒性和 LD 值的测定,评估了衍生物的类药性。在 12 种衍生物中,化合物 、 、 、 和 对 4 种细菌和 2 种真菌具有显著的抗菌和抗真菌活性,最小抑菌浓度值为 40 至 80μg/ml。此外,衍生物的对接评分对 4 种细菌靶标为-8.27 至-11.44kcal/mol,对 2 种真菌靶标为-9.45 至-12.49kcal/mol。因此,从 和 研究来看,百里香酚衍生物可以控制 MRSA、产 ESBL 的细菌和抗真菌耐药真菌。

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