Drug intelligence / Profile preview

isepamicin

Development stage
Unknown
Lead developer
Merck
Modality
Small Molecules
Administration
Intravenous, Intramuscular
01

Overview

Isepamicin is a broad-spectrum, semisynthetic aminoglycoside antibiotic structurally related to gentamicin and amikacin. It exhibits bactericidal activity by inhibiting bacterial protein synthesis through binding to the 30S and 50S ribosomal subunits in susceptible bacteria, leading to faulty or absent proteins. Isepamicin has similar activity to amikacin but demonstrates improved efficacy against certain resistant strains, particularly those producing type I 6'-N-acetyltransferase. Its antibacterial spectrum includes Enterobacteriaceae and staphylococci; it is ineffective against anaerobes, Neisseriaceae, and streptococci. The drug displays a strong concentration-dependent bactericidal effect with a long post-antibiotic effect that allows for once-daily dosing. It is not metabolized and is excreted via the kidneys[1][5][6][7]. Primary indications include treatment of serious bacterial infections such as lower respiratory tract infections, intra-abdominal infections, urinary tract infections, skin and soft tissue infections, and septicemia[5].

Brand names
IsepacinAsepacin
Other names
isepamicine58152-03-7
02

Targets

Bacterial Ribosome

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