Literature DB >> 31882301

Antibacterial activities against Ralstonia solanacearum and Xanthomonas oryzae pv. oryzae of 6-chloro-4-(4-substituted piperazinyl)quinazoline derivatives.

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.
Copyright © 2019 Elsevier Ltd. All rights reserved.

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


  1 in total

1.  Synthesis, X-ray Structure, Hirshfeld, DFT and Biological Studies on a Quinazolinone-Nitrate Complex.

Authors:  Eman M Fathalla; Mezna Saleh Altowyan; Jörg H Albering; Assem Barakat; Morsy A M Abu-Youssef; Saied M Soliman; Ahmed M A Badr
Journal:  Molecules       Date:  2022-02-06       Impact factor: 4.411

  1 in total

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