摘要：For the purpose of screening of inhibitors that are effective for wide range of metallo-β-lactamases, the inhibitory effect of two series of compounds, 2-ω-phenylalkyl-3-mercaptopropionic acid (PhenylC n SH ( n =1—4)) and N -[(7-chloro-quinolin-4-ylamino)-alkyl]-3-mercapto-propionamide (QuinolineC n SH ( n =2—6)), where n denotes the alkyl chain length, on metallo-β-lactamases IMP-1 and VIM-2 was examined. These inhibitors contain a thiol group and a hydrophobic group linked by variable-length methylene chain. PhenylC n SH ( n =1—4) was found to be a potent inhibitor of both IMP-1 and VIM-2. PhenylC4SH was the potent inhibitor of both IMP-1 (IC50=1.2 μ M ) and VIM-2 (IC50=1.1 μ M ) among this study. When the number of methylene units was varied, QuinolineC4SH showed the maximum inhibitory activity against IMP-1 and VIM-2 (IC50=2.5 μ M and IC50=2.4 μ M ). The relationship between the inhibitory effect of the alkyl chain length was different for both series of inhibitors, suggesting that IMP-1 has a tighter binding site than VIM-2. QuinolineCnSH did not serve as a fluorescence reagent for metallo-β-lactamases.
