Clindamycin hydrochloride monohydrate

16 Cited Publications
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Based on 16 publication(s) in Google Scholar

Clindamycin hydrochloride monohydrate is an oral protein synthesis inhibitory agent that has the ability to suppress the expression of virulence factors in Staphylococcus aureus at sub-inhibitory concentrations (sub-MICs). Clindamycin hydrochloride monohydrate resistance results from enzymatic methylation of the antibiotic binding site in the 50S ribosomal subunit (23S rRNA). Clindamycin hydrochloride monohydrate decreases the production of Panton-Valentine leucocidin (PVL), toxic-shock-staphylococcal toxin (TSST-1) or alpha-haemolysin (Hla).

For research use only. We do not sell to patients.

  • Purity : 98.42%
  • CAS No.: 58207-19-5
  • Formula: C18H36Cl2N2O6S
  • Molecular Weight:479.46
  • Storage:

    RT, protect from light.

    In solvent   -80°C, 1 year , -20°C, 6 months
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