SKU: C036  / 
    CAS Number: 24729-96-2

    Clindamycin Phosphate

    $121.00 - $220.50
    • Detailed Description

      CAS Number: 24729-96-2

      Molecular Formula: C18H34ClN2O8PS

      Molecular Weight: 504.96

      Mechanism of Action: Lincosamides inhibit bacterial protein synthesis by binding the 50S ribosomal subunit and interfering with tRNA activity during translation.

      Storage Conditions: Store at room temperature in an airtight container

      Tariff Code: 2941.90.5000

    • Applications

      Spectrum: Clindamycin is a broad-spectrum antibiotic targeting primarily Gram-positive and Gram-negative bacteria such as Clostridium and Bacteroides species. It is also effective against protozoa.

      Microbiology Applications: Clindamycin is commonly used in clinical in vitro microbiological antimicrobial susceptibility tests (panels, discs, and MIC strips) against Gram-positive and Gram-negative anaerobes.  Medical microbiologists use AST results to recommend antibiotic treatment options.  Representative concentration ranges include:

      • Bacteroides fragilis 0.25 µg/mL - 4 µg/ml
      • Clostridium difficile 0.25 µg/mL - 32 µg/mL
      For representative MIC data, click here.

      Eukaryotic Cell Culture Applications: HIV-infected cells (MOLT3 cells) were incubated with increasing concentrations of Clindamycin with no impact on cell death (Wijsman et al, 2013).

      The effects of Clindamycin and its metabolites on mammalian cell lines (mouse leukemia L1210, human oral carcinoma KB, human acute myelogenous leukemia RPMI 6410, and human lymphocyte RPMI 1788) were evaluated. Metabolites clindamycin sulfoxide and clindamycose were nontoxic, whereas N-demethyl clindamycin showed cytotoxic effects in culture (Li et al, 1977).

    • Specifications

      Form: powder

      Appearance: White or almost white crystalline powder

      Source: Semi-synthetic

      Water Content (Karl Fischer): ≤6.0%

      pH: 3.5-4.5

      Assay: ≥758 µg/mg

    • Technical Data

      Solubility: freely soluble in aqueous solution.

    • References

      References:

      Dhawan VK and Thadepalli H (1982)  Clindamycin: A review of fifteen years of experience. Clin. Infect. Dis. 4(6):1133-1153  PMID 6818656

      Li LH, Kuentzel K L, Shugars KD and Bhuyan BK (1977)  Cytotoxicity of several marketed antibiotics on mammalian cells in culture. J. Antibiot (Tokyo) 30(6):506-512  PMID 560364

      Lovmar M and Tanel T (2003)  The mechanism of action of macrolides, lincosamides and streptogramin B reveals the nascent peptide exit path in the ribosome. J. Molec. Microbiol.  330(5 ): 1005-014  PMID 12860123

      Magerlein BJ et al (1966)  Chemical modification of lincomycin. Antimicrob Agents Chemother. 6:727 PMID 5985307

      Wijsman JA, Dekaban GA and Rieder MJ (2013)  Differential toxicity of reactive metabolites of Clindamycin and sulfonamides in HIV-infected cells: Influence of HIV infection on clindamycin toxicity in vitro. J. Clin. Pharmacol. 45(3):346-351  PMID 15703369 

    Clindamycin Phosphate (Clindamycin-2-phosphate) is a broad-spectrum antibiotic and antiparasitic agent.  It is a semi-synthetic derivative of Lincomycin, a natural lincosamide from Streptomyces lincolnensis.  Clindamycin Phosphate is freely soluble in water.

     We also offer:

    • Clindamycin (C233)
    • Clindamycin Hydrochloride (C035)

    CAS Number: 24729-96-2

    Molecular Formula: C18H34ClN2O8PS

    Molecular Weight: 504.96

    Mechanism of Action: Lincosamides inhibit bacterial protein synthesis by binding the 50S ribosomal subunit and interfering with tRNA activity during translation.

    Storage Conditions: Store at room temperature in an airtight container

    Tariff Code: 2941.90.5000

    Spectrum: Clindamycin is a broad-spectrum antibiotic targeting primarily Gram-positive and Gram-negative bacteria such as Clostridium and Bacteroides species. It is also effective against protozoa.

    Microbiology Applications: Clindamycin is commonly used in clinical in vitro microbiological antimicrobial susceptibility tests (panels, discs, and MIC strips) against Gram-positive and Gram-negative anaerobes.  Medical microbiologists use AST results to recommend antibiotic treatment options.  Representative concentration ranges include:

    • Bacteroides fragilis 0.25 µg/mL - 4 µg/ml
    • Clostridium difficile 0.25 µg/mL - 32 µg/mL
    For representative MIC data, click here.

    Eukaryotic Cell Culture Applications: HIV-infected cells (MOLT3 cells) were incubated with increasing concentrations of Clindamycin with no impact on cell death (Wijsman et al, 2013).

    The effects of Clindamycin and its metabolites on mammalian cell lines (mouse leukemia L1210, human oral carcinoma KB, human acute myelogenous leukemia RPMI 6410, and human lymphocyte RPMI 1788) were evaluated. Metabolites clindamycin sulfoxide and clindamycose were nontoxic, whereas N-demethyl clindamycin showed cytotoxic effects in culture (Li et al, 1977).

    Form: powder

    Appearance: White or almost white crystalline powder

    Source: Semi-synthetic

    Water Content (Karl Fischer): ≤6.0%

    pH: 3.5-4.5

    Assay: ≥758 µg/mg

    Solubility: freely soluble in aqueous solution.

    References:

    Dhawan VK and Thadepalli H (1982)  Clindamycin: A review of fifteen years of experience. Clin. Infect. Dis. 4(6):1133-1153  PMID 6818656

    Li LH, Kuentzel K L, Shugars KD and Bhuyan BK (1977)  Cytotoxicity of several marketed antibiotics on mammalian cells in culture. J. Antibiot (Tokyo) 30(6):506-512  PMID 560364

    Lovmar M and Tanel T (2003)  The mechanism of action of macrolides, lincosamides and streptogramin B reveals the nascent peptide exit path in the ribosome. J. Molec. Microbiol.  330(5 ): 1005-014  PMID 12860123

    Magerlein BJ et al (1966)  Chemical modification of lincomycin. Antimicrob Agents Chemother. 6:727 PMID 5985307

    Wijsman JA, Dekaban GA and Rieder MJ (2013)  Differential toxicity of reactive metabolites of Clindamycin and sulfonamides in HIV-infected cells: Influence of HIV infection on clindamycin toxicity in vitro. J. Clin. Pharmacol. 45(3):346-351  PMID 15703369