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Targeting metallo-β-lactamase enzymes in antibiotic resistance.
- Source :
-
Future medicinal chemistry [Future Med Chem] 2013 Jul; Vol. 5 (11), pp. 1243-63. - Publication Year :
- 2013
-
Abstract
- The β-lactam antibiotics are essential for the treatment of a wide range of human bacterial diseases. However, a class of zinc-dependent hydrolases known as the metallo-β-lactamase (MBL) can confer bacteria with extended spectrum β-lactam resistance. To date, there are no clinically approved MBL inhibitors, making these enzymes a serious threat to human health. In this review, a structural approach is taken to outline some of the more promising MBL inhibitors and shed light on how the resistance conferred by this emerging class of enzymes may be circumvented in the future.
- Subjects :
- Aptamers, Nucleotide chemistry
Aptamers, Nucleotide pharmacology
Bacteria enzymology
Carbapenems chemistry
Carbapenems pharmacology
Catalytic Domain
Cephalosporins chemistry
Cephalosporins pharmacology
Cyclobutanes chemistry
Cyclobutanes pharmacology
Enzyme Inhibitors chemistry
Enzyme Inhibitors pharmacology
Humans
Penicillins chemistry
Penicillins pharmacology
Sulfhydryl Compounds chemistry
Sulfhydryl Compounds pharmacology
beta-Lactam Resistance drug effects
beta-Lactamases metabolism
beta-Lactamase Inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1756-8927
- Volume :
- 5
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Future medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 23859206
- Full Text :
- https://doi.org/10.4155/fmc.13.55