Literature DB >> 24239389

Potent and broad-spectrum antibacterial activity of indole-based bisamidine antibiotics: synthesis and SAR of novel analogs of MBX 1066 and MBX 1090.

John D Williams1, Son T Nguyen, Shen Gu, Xiaoyuan Ding, Michelle M Butler, Tommy F Tashjian, Timothy J Opperman, Rekha G Panchal, Sina Bavari, Norton P Peet, Donald T Moir, Terry L Bowlin.   

Abstract

The prevalence of drug-resistant bacteria in the clinic has propelled a concerted effort to find new classes of antibiotics that will circumvent current modes of resistance. We have previously described a set of bisamidine antibiotics that contains a core composed of two indoles and a central linker. The first compounds of the series, MBX 1066 and MBX 1090, have potent antibacterial properties against a wide range of Gram-positive and Gram-negative bacteria. We have conducted a systematic exploration of the amidine functionalities, the central linker, and substituents at the indole 3-position to determine the factors involved in potent antibacterial activity. Some of the newly synthesized compounds have even more potent and broad-spectrum activity than MBX 1066 and MBX 1090.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Amidine; Antibacterial; Antibiotic; Broad-spectrum; Cadogan–Sundberg reaction; Imidazoline; Indole; McMurry reductive homocoupling reaction; Reissert indole synthesis; Tetrahydropyrimidine

Mesh:

Substances:

Year:  2013        PMID: 24239389      PMCID: PMC3906850          DOI: 10.1016/j.bmc.2013.10.014

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


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