Optimization and structure–activity relationships of a series of potent inhibitors of methicillin-resistant Staphylococcus aureus (MRSA) pyruvate kinase as novel antimicrobial agents
| Autor: | Emily Amandoron, B. Brett Finlay, Liam J. Worrall, Nag S. Kumar, Sukhbir Kaur, Lisa Thorson, Huansheng Gong, Roya Zoraghi, Neil E. Reiner, Edwin W. Y. Wong, Raymond H. See, Christophe Labriere, Artem Cherkasov, Anne Moreau, Natalie C. J. Strynadka, Robert N. Young, Linda A. Jackson, Tian Lian |
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| Rok vydání: | 2012 |
| Předmět: |
Methicillin-Resistant Staphylococcus aureus
Models Molecular Enzyme complex medicine.drug_class Pyruvate Kinase Clinical Biochemistry Antibiotics Pharmaceutical Science medicine.disease_cause Biochemistry Microbiology Structure-Activity Relationship Anti-Infective Agents Drug Discovery medicine Humans Structure–activity relationship Protein Kinase Inhibitors Molecular Biology chemistry.chemical_classification biology Organic Chemistry Antimicrobial Enzyme assay Enzyme chemistry Staphylococcus aureus biology.protein Molecular Medicine Pyruvate kinase |
| Zdroj: | Bioorganic & Medicinal Chemistry. 20:7069-7082 |
| ISSN: | 0968-0896 |
| DOI: | 10.1016/j.bmc.2012.10.002 |
| Popis: | A novel series of hydrazones were synthesized and evaluated as inhibitors of methicillin-resistant Staphylococcus aureus (MRSA) pyruvate kinase (PK). PK has been identified as one of the most highly connected 'hub proteins' in MRSA. PK has been shown to be critical for bacterial survival which makes it a potential target for development of novel antibiotics and the high degree of connectivity implies it should be very sensitive to mutations and thus less able to develop resistance. PK is not unique to bacteria and thus a critical requirement for such a PK inhibitor would be that it does not inhibit the homologous human enzyme(s) at therapeutic concentrations. Several MRSA PK inhibitors (including 8d) were identified using in silico screening combined with enzyme assays and were found to be selective for bacterial enzyme compared to four human PK isoforms (M1, M2, R and L). However these lead compounds did not show significant inhibitory activity for MRSA growth presumably due to poor bacterial cell penetration. Structure-activity relationship (SAR) studies were carried out on 8d and led us to discover more potent compounds with enzyme inhibiting activities in the low nanomolar range and some were found to effectively inhibit bacteria growth in culture with minimum inhibitory concentrations (MIC) as low as 1 μg/mL. These inhibitors bind in two elongated flat clefts found at the minor interfaces in the homo-tetrameric enzyme complex and the observed SAR is in keeping with the size and electronic constraints of these binding sites. Access to the corresponding sites in the human enzyme is blocked. |
| Databáze: | OpenAIRE |
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