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Design,synthesis and biological evaluation of sulfenimine cephalosporin sulfoxides as β-lactamase inhibitors 被引量:1
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作者 Kai Zhang Huai-Wei Ding +4 位作者 Hao Ju Qi Huang Li-Juan Zhang Hong-Rui Song de-cai fu 《Chinese Chemical Letters》 SCIE CAS CSCD 2015年第6期801-803,共3页
A series of sulfenimine cephalosporin sulfoxide derivatives (Ta-v) were designed, synthesized and evaluated for their inhibitory activity against TEM-1 and cephalosporinase in cell-free systems. Some of the tested c... A series of sulfenimine cephalosporin sulfoxide derivatives (Ta-v) were designed, synthesized and evaluated for their inhibitory activity against TEM-1 and cephalosporinase in cell-free systems. Some of the tested compounds showed enhanced inhibitory activity against class C β-lactamase cephalospor- inase compared with the tazobactam. The most promising compounds 7c and 7n (IC50 ~ 7.6 and 8.6 μmol/L, respectively) were further investigated in combination with cefradine against a variety of clinical isolated fi-lactamase-producing bacterial strains. 展开更多
关键词 β-Lactamase inhibitor Sulfenimine Synthesis
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