| Literature DB >> 26460684 |
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.Entities:
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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