Description
Midecamycin is a macrolide antibiotic similar in structure to erythromycin. Midecamycin is soluble in methanol, ethanol, and acidic solutions.
Mechanism
Midecamycin inhibits bacterial growth by targeting the 50S ribosomal subunit preventing peptide bond formation and translocation during protein synthesis. Resistance to midecamycin is commonly attributed to mutations in 50S rRNA preventing midecamycin binding allowing the cell to synthesize proteins free of error.
Spectrum
Midecamycin is a broad spectrum antibiotic targeting a wide range of bacteria especially those which cause respiratory, ear, and skin infections.
Form
Powder
Purity Level
>900 μg/mg
Related Documents
References
Morikawa, K. "Immunomodulatory Effects of Three Macrolides, Midecamycin Acetate, Josamycin, and Clarithromycin, on Human T-lymphocyte Function in Vitro." Antimicrobial Agents and Chemotherapy 38.11 (1994): 2643-647. Ncbi.gov. Web. 18 Sept. 2012.
Lovmar, Martin, and Tanel Tenson. "The Mechanism of Action of Macrolides, Lincosamides and Streptogramin B Reveals the Nascent Peptide Exit Path in the Ribosome."Journal of Molecular Microbiology 330.5 (2003): 1005-014.