The synthesis and SAR of rhodanines as novel class C β-lactamase inhibitors

Bioorganic and Medicinal Chemistry Letters

Volumn 10, Issue 19, 2000, Pages 2179-2182

  Grant, Eugene B ^a   Guiadeen, Deodialsingh ^a   Baum, Ellen Z ^a   Foleno, Barbara D ^a   Jin, Haiyong ^a   Montenegro, Deborah A ^a   Nelson, Erin A ^a   Bush, Karen ^a   Hlasta, Dennis J ^a  

^a R W JOHNSON PHARMACEUTICAL RES I   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BETA LACTAMASE INHIBITOR; CEPHALOSPORIN DERIVATIVE; PENICILLIN DERIVATIVE; PIPERACILLIN; RHODANINE;

ANTIMICROBIAL ACTIVITY; ARTICLE; CONTROLLED STUDY; DRUG POTENCY; DRUG POTENTIATION; DRUG SCREENING; DRUG SELECTIVITY; DRUG SENSITIVITY; DRUG SYNTHESIS; HYDROLYSIS; MINIMUM INHIBITORY CONCENTRATION; NONHUMAN; STRUCTURE ACTIVITY RELATION;

BETA-LACTAMASES; DRUG EVALUATION, PRECLINICAL; ENZYME INHIBITORS; MOLECULAR STRUCTURE; PIPERACILLIN; RHODANINE; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 0034597074     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(00)00444-3     Document Type: Article

References (14)