BMJ · 1960 · 40 citations · 4 references
PharmacyChemistryMicrobiologyDrug DiscoveryOrganic ChemistryStructure-activity RelationshipsAntibacterial PharmacologyAntibiotic ProductionStructure-activity Relationship AnalysisAntibacterial Drug DevelopmentAntibiotic DiscoveryNovel Antibacterial Drug Discovery
A report in 1959 by Batchelor et al. on the isolation of 6-aminopenicillanic acid drew attention to the possibility of synthesizing new forms of penicillin by the introduction of side-chains. Derivatives prepared in this way may or may not possess antibacterial activity, but we were particularly impressed by the range and mode of action of one derivative, supplied to us in 1959 as BRL 1241 (" celbenin "). The compound-sodium 6- (2,6 dimethoxybenzamido)penicillanate monohydrate- may be represented by the following structural formula: OCH3 s /CH3
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Synthesis of Penicillin: 6-Aminopenicillanic Acid in Penicillin Fermentations
F. R. Batchelor, F. P. Doyle, J. H. C. Nayler et al. · Nature · 1959 · 389 citations
A New Penicillin (BRL 1241) Active Against Penicillin-resistant Staphylococci
Robert Knox · BMJ · 1960 · 67 citations · Full text
Report on Clinical Use of BRL 1241 in Children with Staphylococcal and Streptococcal Infections
Gordon T. Stewart, H.H. Nixon, Hannah Coles et al. · BMJ · 1960 · 37 citations · Full text