Date published: 2026-4-28

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Retapamulin (CAS 224452-66-8)

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Alternate Names:
Rebapamulin; SB 275833
Application:
Retapamulin is a broad spectrum antibiotic with no cross resistance to existing classes
CAS Number:
224452-66-8
Molecular Weight:
517.76
Molecular Formula:
C30H47NO4S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Retapamulin, with the CAS number 224452-66-8, is a semisynthetic derivative of the pleuromutilin class of antibiotics, originally derived from the fungus Clitopilus passeckerianus. It is distinctively known for its unique mechanism of action, which involves binding to the peptidyl transferase center within the 50S subunit of bacterial ribosomes. This binding interferes with the synthesis of proteins by preventing the formation of peptide bonds between amino acids, which is a crucial step in the translation process. Unlike many other antibiotics that target the ribosome, retapamulin selectively inhibits the growth of bacterial cells by acting at a site that differs slightly from those affected by other antibiotics, reducing the cross-resistance with drugs targeting other parts of the ribosome. In research settings, retapamulin has been used as a tool to study protein synthesis and to explore the mechanistic underpinnings of ribosomal function and inhibition. It has also been instrumental in investigating how modifications at the peptidyl transferase center impact the efficacy and selectivity of ribosomal inhibitors. This research is crucial for understanding bacterial resistance mechanisms and for designing novel inhibitors that can bypass existing resistance pathways in pathogenic bacteria.


Retapamulin (CAS 224452-66-8) References

  1. In vitro activity of retapamulin against Staphylococcus aureus isolates resistant to fusidic acid and mupirocin.  |  Woodford, N., et al. 2008. J Antimicrob Chemother. 62: 766-8. PMID: 18567573
  2. In vitro activities of retapamulin and 16 other antimicrobial agents against recently obtained Streptococcus pyogenes isolates.  |  Pérez-Trallero, E., et al. 2011. Antimicrob Agents Chemother. 55: 2406-8. PMID: 21343452
  3. In vitro activity of retapamulin against linezolid and methicillin-resistant Staphylococcus aureus isolates.  |  Candel, FJ., et al. 2011. Rev Esp Quimioter. 24: 127-30. PMID: 21947094
  4. In Vitro Activity of Retapamulin against Staphylococcus aureus Resistant to Various Antimicrobial Agents.  |  Saravolatz, LD., et al. 2013. Antimicrob Agents Chemother. 57: 4547-4550. PMID: 23796931
  5. Efficacy of topical and systemic antibiotic treatment of meticillin-resistant Staphylococcus aureus in a murine superficial skin wound infection model.  |  Vingsbo Lundberg, C. and Frimodt-Møller, N. 2013. Int J Antimicrob Agents. 42: 272-5. PMID: 23837927
  6. In Vitro Antimicrobial Activities of Fusidic Acid and Retapamulin against Mupirocin- and Methicillin-Resistant Staphylococcus aureus.  |  Park, SH., et al. 2015. Ann Dermatol. 27: 551-6. PMID: 26512169
  7. In Vitro Activity of Retapamulin and Antimicrobial Susceptibility Patterns in a Longitudinal Collection of Methicillin-Resistant Staphylococcus aureus Isolates from a Veterans Affairs Medical Center.  |  Harrington, AT., et al. 2015. Antimicrob Agents Chemother. 60: 1298-303. PMID: 26666950
  8. Retapamulin-Assisted Ribosome Profiling Reveals the Alternative Bacterial Proteome.  |  Meydan, S., et al. 2019. Mol Cell. 74: 481-493.e6. PMID: 30904393
  9. In vitro synergistic effect of retapamulin with erythromycin and quinupristin against Enterococcus faecalis.  |  Park, B. and Min, YH. 2020. J Antibiot (Tokyo). 73: 630-635. PMID: 32346089
  10. Erythromycin, retapamulin, pyridoxine, folic acid, and ivermectin inhibit cytopathic effect, papain-like protease, and MPRO enzymes of SARS-CoV-2.  |  Bello, SO., et al. 2023. Front Cell Infect Microbiol. 13: 1273982. PMID: 38089816

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Retapamulin, 1 mg

sc-391696
1 mg
$170.00