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Overview
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Virginiamycin is a streptogramin, and a mixture of Virginiamycin M1 and Virginiamycin S1. The commercial mixture is 75% Virginiamycin M1 and 25 % Virginiamycin S1, along with less abundant S analogs. The two components of the mixture have differing solubilities, which can affect the binding to the 50S ribosome, which in turn influences the bacteriostatic effects. Virginiamycin is soluble in DMSO and DMF.
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Background
Virginiamycin inhibits protein synthesis, targeting to the 50S ribosome and inducing a conformational change at the peptidyl transferase center. Protein synthesis is inhibited in both actively growing and static bacterial cells.
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Overview