Drug intelligence / Profile preview

oleandomycin

Development stage
Discontinued
Lead developer
Pfizer
Modality
Small Molecules
Administration
Oral, Intravenous, Intramuscular, Topical
01

Overview

Oleandomycin is a macrolide antibiotic originally isolated from Streptomyces antibioticus. It is structurally related to erythromycin but is less effective due to the absence of a 12-hydroxyl group and a 3-methoxy group. Mechanistically, oleandomycin acts as a bacteriostatic agent by binding to the 50S subunit of bacterial ribosomes, inhibiting protein synthesis necessary for bacterial survival and replication. Its spectrum of activity includes most gram-positive bacteria (such as Staphylococci and Streptococci), with limited effect on gram-negative bacteria and rickettsiae. Clinically, it has been used for infections like pyoderma, sepsis, meningitis, respiratory tract infections, urinary tract infections, and other conditions caused by susceptible organisms. Currently in the United States it is approved only for veterinary use in swine and poultry production[1][3][4][8].

Brand names
MatromycinRomicilSigmamycin
Other names
Oleandomycin phosphateOleandomycin HClOleandomycin hydrochloride
02

Targets

Bacterial 50S ribosomal subunit

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