Clindamycin-13C,d3 is a stable isotope-labeled form of the lincosamide antibiotic Clindamycin, which primarily targets bacterial protein synthesis. This compound exhibits broad-spectrum bacteriostatic activity, effectively suppressing virulence factors in Staphylococcus aureus at sub-inhibitory concentrations. It plays a significant role in research on antibiotic resistance mechanisms, particularly concerning enzymatic methylation impacting the 50S ribosomal subunit. Additionally, Clindamycin-13C,d3 can be utilized in studies investigating malaria.
Clindamycin-13C,d3 is a stable isotope-labeled form of the lincosamide antibiotic Clindamycin, which primarily targets bacterial protein synthesis. This compound exhibits broad-spectrum bacteriostatic activity, effectively suppressing virulence factors in Staphylococcus aureus at sub-inhibitory concentrations. It plays a significant role in research on antibiotic resistance mechanisms, particularly concerning enzymatic methylation impacting the 50S ribosomal subunit. Additionally, Clindamycin-13C,d3 can be utilized in studies investigating malaria.
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