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Biological Activity of Antibiotic G-418, a New Micromonospora-produced Aminoglycoside with Activity Against Protozoa and Helminths

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Specialty Pharmacology
Date 1974 Nov 1
PMID 15825308
Citations 5
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Abstract

On the basis of parallel in vitro studies with antibiotic G-418, gentamicin, neomycin, and kanamycin, antibiotic G-418 was found to be less potent than gentamicin but more active than either kanamycin or neomycin against most strains, with the exception of Pseudomonas, for which neomycin was more active than antibiotic G-418, and enterococci, for which antibiotic G-418 was more active than the other three antibiotics. Mouse protection tests indicated that antibiotic G-418 is approximately half as potent as gentamicin and its acute toxicity is one-half to one-third that of gentamicin.

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References
1.
Wagman G, Testa R, Marquez J, Weinstein M . Antibiotic G-418, a new Micromonospora-produced aminoglycoside with activity against protozoa and helminths: fermentation, isolation, and preliminary characterization. Antimicrob Agents Chemother. 1974; 6(2):144-9. PMC: 444619. DOI: 10.1128/AAC.6.2.144. View

2.
Waitz J, Moss Jr E, Drube C, Weinstein M . Comparative activity of sisomicin, gentamicin, kanamycin, and tobramycin. Antimicrob Agents Chemother. 1972; 2(6):431-7. PMC: 444335. DOI: 10.1128/AAC.2.6.431. View