| Literature DB >> 27139465 |
Tsukasa Ito-Horiyama1, Yoshikazu Ishii2, Akinobu Ito1, Takafumi Sato3, Rio Nakamura1, Norio Fukuhara4, Masakatsu Tsuji1, Yoshinori Yamano1, Keizo Yamaguchi2, Kazuhiro Tateda2.
Abstract
To better understand the antibacterial activity of S-649266 against carbapenemase producers, its stability against clinically relevant carbapenemases was investigated. The catalytic efficiencies (kcat/Km) of IMP-1, VIM-2, and L1 for S-649266 were 0.0048, 0.0050, and 0.024 μM(-1) s(-1), respectively, which were more than 260-fold lower than that for meropenem. Only slight hydrolysis of S-649266 against KPC-3 was observed. NDM-1 hydrolyzed meropenem 3-fold faster than S-649266 at 200 μM.Entities:
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Year: 2016 PMID: 27139465 PMCID: PMC4914688 DOI: 10.1128/AAC.03098-15
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191