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Antimicrobial N-(2-chlorobenzyl)-substituted hydroxamate is an inhibitor of 1-deoxy-D-xylulose 5-phosphate synthase

机译:抗菌N-(2-氯苄基)取代的异羟肟酸酯是1-脱氧-D-木酮糖5-磷酸合酶的抑制剂

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摘要

N-(2-Chlorobenzyl)-substituted hydroxamate, readily produced by hydrolysis of ketoclomazone, was identified as an inhibitor of 1-deoxy-D-xylulose 5-phosphate synthase (DXS), with an IC_(50) value of 1.0 μM. The compound inhibited the growth of Haemophilus influenzae. A convenient spectroscopic method for assaying DXS using NADPH-lactate dehydrogenase (LDH) is also reported.
机译:N-(2-氯苄基)取代的异羟肟酸酯很容易通过酮康唑酮的水解产生,被鉴定为1-脱氧-D-木酮糖5-磷酸合酶(DXS)的抑制剂,IC_(50)值为1.0μM。该化合物抑制流感嗜血杆菌的生长。还报道了使用NADPH-乳酸脱氢酶(LDH)测定DXS的简便光谱方法。

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  • 来源
    《Chemical Communications》 |2013年第49期|5535-5537|共3页
  • 作者单位

    The Institute of Scientific and Industrial Research (ISIR), Osaka University,8-1 Mihogaoka, Ibaraki, Osaka 567-0047, Japan;

    The Institute of Scientific and Industrial Research (ISIR), Osaka University,8-1 Mihogaoka, Ibaraki, Osaka 567-0047, Japan;

    Biotechnology Research Center, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku,Tokyo 113-8657, Japan;

    R&D Administration, Pharmaceuticals, Meiji Seiko. Kaisha, 2-4-16, Kyobashi,Chuo-ku, Tokyo 104-8002, Japan;

    The Institute of Scientific and Industrial Research (ISIR), Osaka University,8-1 Mihogaoka, Ibaraki, Osaka 567-0047, Japan;

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  • 入库时间 2022-08-17 13:18:26

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