Literature DB >> 26460684

Discovery of Azaindole Ureas as a Novel Class of Bacterial Gyrase B Inhibitors.

Jing Zhang1, Qingyi Yang1, Jason B Cross1, Jan Antoinette C Romero1, Katherine M Poutsiaka1, Felix Epie1, Douglas Bevan1, Bin Wang1, Yanzhi Zhang1, Ajit Chavan1, Xin Zhang1, Terence Moy1, Anu Daniel1, Kien Nguyen1, Brian Chamberlain1, Nicole Carter1, Joseph Shotwell1, Jared Silverman1, Chester A Metcalf1, Dominic Ryan1, Blaise Lippa1, Roland E Dolle1.   

Abstract

The emergence and spread of multidrug resistant bacteria are widely believed to endanger human health. New drug targets and lead compounds exempt from cross-resistance with existing drugs are urgently needed. We report on the discovery of azaindole ureas as a novel class of bacterial gyrase B inhibitors and detail the story of their evolution from a de novo design hit based on structure-based drug design. These inhibitors show potent minimum inhibitory concentrations against fluoroquinolone resistant MRSA and other Gram-positive bacteria.

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Year:  2015        PMID: 26460684     DOI: 10.1021/acs.jmedchem.5b00961

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  2 in total

1.  Formal aromaticity transfer for palladium-catalyzed coupling between phenols and pyrrolidines/indolines.

Authors:  Zihang Qiu; Jiang-Sheng Li; Chao-Jun Li
Journal:  Chem Sci       Date:  2017-08-10       Impact factor: 9.825

2.  New N-phenylpyrrolamide DNA gyrase B inhibitors: Optimization of efficacy and antibacterial activity.

Authors:  Martina Durcik; Denise Lovison; Žiga Skok; Cristina Durante Cruz; Päivi Tammela; Tihomir Tomašič; Davide Benedetto Tiz; Gábor Draskovits; Ákos Nyerges; Csaba Pál; Janez Ilaš; Lucija Peterlin Mašič; Danijel Kikelj; Nace Zidar
Journal:  Eur J Med Chem       Date:  2018-05-10       Impact factor: 6.514

  2 in total

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