Drug intelligence / Profile preview

norvancomycin

Development stage
Unknown
Lead developer
North China Pharmaceutical
Modality
Antimicrobial Peptides → Native Peptides → Peptides, Cyclic Peptides → Modified Peptides → Peptides, Small Molecules
Administration
Intravenous
01

Overview

Norvancomycin is a glycopeptide antibiotic closely related to vancomycin, differing by a single methyl group. It was first isolated from Amycolatopsis orientalis and has been used clinically in China since the late 1960s. Norvancomycin acts by inhibiting bacterial cell wall synthesis, making it effective against resistant Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA). Its primary indications include severe infections such as endocarditis, osteomyelitis, pneumonia, sepsis, and soft tissue infections caused by susceptible organisms. Norvancomycin is typically administered intravenously[1][2][5][7].

Brand names
norvancomycin
Other names
desmethylvancomycin56-demethylvancomycin
02

Targets

D-Ala-D-Ala (D-Ala-D-Ala terminus)

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