| Literature DB >> 31882301 |
Wu-Bin Shao1, Yu-Tao Zheng1, Jia-Min Liu2, Yi-Hong Fu2, Pu-Ying Qi1, Xiang Zhou1, Zhi-Bing Wu1, Pei-Yi Wang3, Song Yang4.
Abstract
In this letter, a variety of simple 6-chloro-4-(4-substituted piperazinyl)quinazoline derivatives was prepared. Preliminary bioassays revealed that these compounds showed good antibacterial activities toward phytopathogens Ralstonia solanacearum and Xanthomonas oryzae pv. oryzae (Xoo). Among these derivatives, compounds 5a, 5d, 5e, 5f, 5p, 5q, 6b, and 6d exhibited potent inhibition effects against R. solanacearum with EC50 within 4.60-9.94 µg/mL, especially, compound 5g exerted the strongest activity with EC50 of 2.72 µg/mL; compound 6b possessed the best inhibitory activity toward Xoo with EC50 of 8.46 µg/mL. Subsequently, a good predictive three-dimensional quantitative structure-activity relationship (3D-QSAR) model was constructed via CoMFA to direct the future structural modification and optimization. Furthermore, the pathogens' topological studies were performed to explore the possible antibacterial mechanism. Given their simple frameworks and facile synthesis, title compounds can serve as the potential antibacterial leads.Entities:
Keywords: 3D-QSAR; Antibacterial; Morphological studies; Quinazoline; Synthesis
Year: 2019 PMID: 31882301 DOI: 10.1016/j.bmcl.2019.126912
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823