Recent advances in the chemistry of β-lactam compounds as selected active-site serine β-lactamase inhibitors

Current Pharmaceutical Design

Volumn 5, Issue 11, 1999, Pages 939-953

  Mascaretti, Oreste A ^a   Danelon, Gerardo O ^a   Setti, Eduardo L ^a,b   Laborde, María ^a   Mata, Ernesto G ^a  

^a Universidad Nacional de Rosario   (Argentina)

^b Axys Pharmaceuticals Inc   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BETA LACTAMASE INHIBITOR;

ANTIBACTERIAL ACTIVITY; ANTIBODY DIRECTED ENZYME PRODRUG THERAPY; CRYSTAL STRUCTURE; DRUG EFFECT; DRUG STABILITY; ENZYME ACTIVE SITE; ENZYME ACTIVITY; ENZYME INHIBITOR COMPLEX; ENZYME MECHANISM; HYDROLYSIS; MEMBRANE BINDING; PRIORITY JOURNAL; REVIEW;

ANTI-BACTERIAL AGENTS; BETA-LACTAMASES; BETA-LACTAMS; BINDING SITES; ENZYME INHIBITORS; GRAM-NEGATIVE BACTERIA; HYDROLYSIS; SERINE; STEREOISOMERISM;

EID: 0032719252     PISSN: 13816128     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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