Issue 19, 2019

Antibacterial activity and mechanism of action of a thiophenyl substituted pyrimidine derivative

Abstract

The issue of multidrug resistant bacteria is a worldwide health threat. To develop new antibacterial agents with new mechanisms of action is thus an urgent request to address this antibiotic resistance crisis. In the present study, a new thiophenyl-pyrimidine derivative was prepared and utilized as an effective antibacterial agent against Gram-positive strains. In the tests against MRSA and VREs, the compound showed higher antibacterial potency than that of vancomycin and methicillin. The mode of action is probably attributed to the effective inhibition of FtsZ polymerization, GTPase activity, and bacterial cell division, which cause bactericidal effects. The compound could be a potential candidate for further development as an effective antibiotic to combat drug-resistant bacteria.

Graphical abstract: Antibacterial activity and mechanism of action of a thiophenyl substituted pyrimidine derivative

Supplementary files

Article information

Article type
Paper
Submitted
07 Feb 2019
Accepted
02 Apr 2019
First published
05 Apr 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 10739-10744

Antibacterial activity and mechanism of action of a thiophenyl substituted pyrimidine derivative

Z. Fang, Y. Li, Y. Zheng, X. Li, Y. Lu, S. Yan, W. Wong, K. Chan, K. Wong and N. Sun, RSC Adv., 2019, 9, 10739 DOI: 10.1039/C9RA01001G

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements