Drug intelligence / Profile preview

dibekacin

Development stage
Phase 4
Lead developer
Meiji Seika Pharma
Modality
Small Molecules
Administration
Intramuscular, Intravenous
01

Overview

Dibekacin is a semisynthetic aminoglycoside antibiotic derived from kanamycin B. It acts by binding to the 30S and 50S subunits of bacterial ribosomes, inhibiting protein synthesis and causing errors in genetic code transcription that lead to bacterial cell death. Dibekacin is effective against gram-negative aerobes and some strains of Staphylococci, including those resistant to kanamycin. It is primarily used for severe infections caused by susceptible bacteria and has been marketed mainly in Japan. The drug is administered parenterally (intramuscularly or intravenously) for systemic infections[1][2][3][4].

Brand names
PanamicinDibekacin Meiji
Other names
dibekacinadibekacinedibekacinum
02

Targets

Bacterial RibosomeBacterial 50S ribosomal subunit

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