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Overview
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Erythromycin Thiocyanate is the thiocyanate form of the broad-spectrum macrolide antibiotic Erythromycin. It was discovered in 1952 from Saccharopolyspora erythraea (formerly Streptomyces erythraeus). Erythromycin acts by inhibiting bacterial protein synthesis.
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Background
Macrolide antibiotics inhibit bacterial growth by targeting the 50S ribosomal subunit preventing peptide bond formation and translocation during protein synthesis. Resistance to erythromycin is commonly attributed to mutations in 50S rRNA preventing erythromycin binding allowing the cell to synthesize proteins free of error. Erythromycin is also a splicing inhibitor of eukaryotic nuclear pre-mRNA, almost completely inhibiting the formation of the splicing-active C complex.
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Overview