1. Anti-infection
  2. Bacterial
  3. Clindamycin hydrochloride monohydrate

Clindamycin hydrochloride monohydrate 

Cat. No.: HY-N7118
Handling Instructions

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.

Clindamycin hydrochloride monohydrate Chemical Structure

Clindamycin hydrochloride monohydrate Chemical Structure

CAS No. : 58207-19-5

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Description

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)[1].

Molecular Weight

479.46

Formula

C₁₈H₃₆Cl₂N₂O₆S

CAS No.

58207-19-5

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Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

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Clindamycin hydrochloride monohydrate
Cat. No.:
HY-N7118
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