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Discovery of Azaindole Ureas as a Novel Class of Bacterial Gyrase B Inhibitors.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2015 Nov 12; Vol. 58 (21), pp. 8503-12. Date of Electronic Publication: 2015 Oct 22. - Publication Year :
- 2015
-
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.
- Subjects :
- Bacterial Proteins metabolism
Crystallography, X-Ray
Gram-Positive Bacteria drug effects
Gram-Positive Bacteria enzymology
Gram-Positive Bacterial Infections drug therapy
Gram-Positive Bacterial Infections microbiology
Humans
Indoles chemistry
Methicillin-Resistant Staphylococcus aureus drug effects
Models, Molecular
Staphylococcal Infections drug therapy
Staphylococcal Infections microbiology
Topoisomerase II Inhibitors chemistry
Urea analogs & derivatives
Bacterial Proteins antagonists & inhibitors
DNA Gyrase metabolism
Indoles pharmacology
Methicillin-Resistant Staphylococcus aureus enzymology
Topoisomerase II Inhibitors pharmacology
Urea pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4804
- Volume :
- 58
- Issue :
- 21
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 26460684
- Full Text :
- https://doi.org/10.1021/acs.jmedchem.5b00961