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Antimicrobial N-(2-chlorobenzyl)-substituted hydroxamate is an inhibitor of 1-deoxy-D-xylulose 5-phosphate synthase.
Chemical Communications ( IF 4.3 ) Pub Date : 2013 Jun 21 , DOI: 10.1039/c3cc40758f Daisuke Hayashi , Nobuo Kato , Tomohisa Kuzuyama , Yasuo Sato , Junko Ohkanda
Chemical Communications ( IF 4.3 ) Pub Date : 2013 Jun 21 , DOI: 10.1039/c3cc40758f Daisuke Hayashi , Nobuo Kato , Tomohisa Kuzuyama , Yasuo Sato , Junko Ohkanda
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 IC50 value of 1.0 muM. The compound inhibited the growth of Haemophilus influenzae. A convenient spectroscopic method for assaying DXS using NADPH-lactate dehydrogenase (LDH) is also reported.
中文翻译:
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。
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而产生,被鉴定为1-脱氧-D-木酮糖5-磷酸合酶(DXS)的抑制剂,IC50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。
更新日期:2017-01-31
中文翻译:
![](https://scdn.x-mol.com/jcss/images/paperTranslation.png)
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。
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而产生,被鉴定为1-脱氧-D-木酮糖5-磷酸合酶(DXS)的抑制剂,IC50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。