Literature DB >> 26522949

Structure-activity relationship of indoloquinoline analogs anti-MRSA.

Min Zhao1, Tomonori Kamada1, Aya Takeuchi1, Hiromi Nishioka1, Teruo Kuroda1, Yasuo Takeuchi2.   

Abstract

Indolo[3,2-b]quinoline analogs (3a-3s), 4-(acridin-9-ylamino) phenol hydrochloride (4), benzofuro[3,2-b]quinoline (3t), indeno[1,2-b]quinolines (3u and 3v) have been synthesized. Those compounds were found to exhibit anti-bacterial activity towards Methicillin-resistant Staphylococcus aureus (anti-MRSA activity). Structure-activity relationship studies were conducted that indoloquinoline ring, benzofuroquinoline ring and 4-aminophenol group are essential structure for anti-MRSA activity.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Anti-MRSA; Benzofuroquinoline; Indenoquinoline; Indoloquinoline; Structure–activity

Mesh:

Substances:

Year:  2015        PMID: 26522949     DOI: 10.1016/j.bmcl.2015.10.058

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

1.  Synthesis and antimicrobial studies of novel derivatives of 4-(4-formyl-3-phenyl-1H-pyrazol-1-yl)benzoic acid as potent anti-Acinetobacter baumannii agents.

Authors:  Devin Allison; Evan Delancey; Hunter Ramey; Conrad Williams; Zakeyah Ali Alsharif; Hessa Al-Khattabi; Allyn Ontko; David Gilmore; Mohammad A Alam
Journal:  Bioorg Med Chem Lett       Date:  2016-12-29       Impact factor: 2.823

Review 2.  A review on quinoline derivatives as anti-methicillin resistant Staphylococcus aureus (MRSA) agents.

Authors:  Pradeep Kumar
Journal:  BMC Chem       Date:  2020-03-13
  2 in total

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