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INHIBITOR FOR CARBAPENEM HYDROLYSIS CLASS D BETA-LACTAMASE (CHDL) AND PREPARATION METHOD THEREOF

机译:碳烯烃水解级Dβ-内酰胺酶(CHDL)的抑制剂及其制备方法

摘要

The present invention relates to an inhibitor for carbapenem hydrolysis class D beta-lactamase and a preparation method thereof and, more particularly, to [3-(2-phenylethoxy)phenyl]boronic acid or a pharmaceutically acceptable salt thereof for inhibiting CHDL, and a preparation method thereof. [3-(2-phenylethoxy)phenyl]boronic acid or a pharmaceutically acceptable salt thereof according to the present invention inhibits all six clinically important subgroups of CHDL and four newly emerging CHDL subgroups. Accordingly, the compound according to the present invention inhibits a wide variety of CHDLs such that when used together with beta-lactam antibiotics, the compound is effective for treatment of infections caused by bacteria that develop antibiotic resistance due to various CHDLs.
机译:本发明涉及碳烯烃水解级别Dβ-内酰胺酶的抑制剂及其制备方法,更具体地,涉及[3-(2-苯基乙氧基)苯基]硼酸或其药学上可接受的盐,用于抑制CHDL,以及其制备方法。 [3-(2-苯乙氧氧基)苯基]硼酸或其药学上可接受的盐根据本发明抑制了CHDL和四个新出现的CHDL亚组的所有六个临床上重要的亚组。因此,根据本发明的化合物抑制各种CHDL,使得当与β-内酰胺抗生素一起使用时,该化合物对于治疗由各种CHDL产生抗生素抗性引起的感染是有效的。

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