Streptomycin hydrochloride

A thiazole-containing peptide antibiotic that inhibits protein synthesis by preventing binding of GTP to 50S ribosomal subunit. Inhibits the function of elongation factor G (EF-G) and the dissociation of EF-G from the ribosome.

A thiazole-containing peptide antibiotic that inhibits protein synthesis by preventing binding of GTP to 50S ribosomal subunit. Inhibits the function of elongation factor G (EF-G) and the dissociation of EF-G from the ribosome.

General DescriptionChemical structure: glycopeptideApplicationVancomycin has been used to study transcriptional induction of the penicillin-binding protein 2 gene in Staphylococcus aureus , the correlation of vancomycin and daptomycin susceptibility

General DescriptionChemical structure: glycopeptideApplicationVancomycin has been used to study transcriptional induction of the penicillin-binding protein 2 gene in Staphylococcus aureus , the correlation of vancomycin and daptomycin susceptibility

General DescriptionChemical structure: glycopeptideApplicationVancomycin has been used to study transcriptional induction of the penicillin-binding protein 2 gene in Staphylococcus aureus , the correlation of vancomycin and daptomycin susceptibility

General DescriptionVancomycin is a heptapeptide. Chemical structure: glycopeptideApplicationVancomycin hydrochloride from Streptomyces orientalis has been used as: an antibiotic in screening: minimal inhibitory concentrations (MICs) Streptomyces

General DescriptionVancomycin is a heptapeptide. Chemical structure: glycopeptideApplicationVancomycin hydrochloride from Streptomyces orientalis has been used as: an antibiotic in screening: minimal inhibitory concentrations (MICs) Streptomyces