Anhydrolide macrolides. 2. Synthesis and antibacterial activity of 2,3- anhydro-6-O-methyl 11,12-carbazate erythromycin A analogues

Journal of Medicinal Chemistry

Volumn 41, Issue 10, 1998, Pages 1660-1670

  Griesgraber, George ^a,b   Kramer, Mark J ^a   Elliott, Richard L ^a   Nilius, Angela M ^a   Ewing, Patty J ^a   Raney, Patti M ^a   Bui, Mai Ha ^a   Flamm, Robert K ^a   Chu, Daniel T W ^a   Plattner, Jacob J ^a   Or, Yat Sun ^a  

^a ABBOTT LABORATORIES   (United States)

^b Dept 47N ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

2,3 ANHYDRO 6 O METHYL 11,12 CARBAMATE ERYTHROMYCIN A; ERYTHROMYCIN DERIVATIVE; MACROLIDE; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ANTIBIOTIC SENSITIVITY; ARTICLE; DRUG DEGRADATION; DRUG POTENCY; DRUG SAFETY; DRUG SYNTHESIS; GENE REARRANGEMENT; INTESTINE MOTILITY; METHYLATION; NONHUMAN; PEPTIC ULCER;

ANIMALS; ANTI-BACTERIAL AGENTS; CLARITHROMYCIN; DRUG EVALUATION, PRECLINICAL; DRUG RESISTANCE, MICROBIAL; DRUG RESISTANCE, MULTIPLE; ERYTHROMYCIN; MACROLIDES; MICE; PNEUMOCOCCAL INFECTIONS; STAPHYLOCOCCAL INFECTIONS; STAPHYLOCOCCUS AUREUS; STREPTOCOCCUS PNEUMONIAE; STREPTOCOCCUS PYOGENES; STRUCTURE-ACTIVITY RELATIONSHIP; VIRGINIAMYCIN;

EID: 15144341622     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm970548p     Document Type: Article

References (22)

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