Clindamycin-d3 hydrochloride is a deuterium-labeled derivative of Clindamycin, a bacteriostatic lincosamide antibiotic that primarily targets bacterial protein synthesis. It is effective against a wide range of bacteria, including Staphylococcus aureus, and can suppress the expression of critical virulence factors at sub-inhibitory concentrations. Furthermore, it can be utilized in studies related to Clindamycin resistance and its effects on the production of Panton-Valentine leucocidin, toxic-shock-staphylococcal toxin, and alpha-haemolysin. Additionally, Clindamycin-d3 hydrochloride serves as a valuable tool in malaria research, facilitating investigations into antibiotic effects and resistance mechanisms.
Clindamycin-d3 hydrochloride is a deuterium-labeled derivative of Clindamycin, a bacteriostatic lincosamide antibiotic that primarily targets bacterial protein synthesis. It is effective against a wide range of bacteria, including Staphylococcus aureus, and can suppress the expression of critical virulence factors at sub-inhibitory concentrations. Furthermore, it can be utilized in studies related to Clindamycin resistance and its effects on the production of Panton-Valentine leucocidin, toxic-shock-staphylococcal toxin, and alpha-haemolysin. Additionally, Clindamycin-d3 hydrochloride serves as a valuable tool in malaria research, facilitating investigations into antibiotic effects and resistance mechanisms.
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