期刊
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 24, 期 19, 页码 4689-4693出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2014.08.030
关键词
Antibiotics; Bioisosteres; Inhibitors; Ligases; Drug design
资金
- National Health and Medical Research Council (NHMRC) [APP1011806, APP1068885]
Inhibitors of Staphylococcus aureus biotin protein ligase (SaBPL) are generated by replacing the acyl phosphate group of biotinyl-5'-AMP with either a 1,2,3-triazole (see 5/10a/10b) or a 1,2,4-oxadiazole (see 7) bioisostere. Importantly, the inhibitors are inactive against the human BPL. The nature of the 5-substituent in the component benzoxazolone of the optimum 1,2,3-triazole series is critical to activity, where this group binds in the ATP binding pocket of the enzyme. (C) 2014 Elsevier Ltd. All rights reserved.
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