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Contents

   



(Top)
 


1 Indications  





2 Pharmacology  



2.1  Mechanism of action  





2.2  Pharmacokinetics  







3 Contraindications  





4 Adverse reactions  





5 References  














Retapamulin






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From Wikipedia, the free encyclopedia
 


Retapamulin
Clinical data
Trade namesAltabax, Altargo
AHFS/Drugs.comMonograph
MedlinePlusa607049
License data
  • US FDARetapamulin
  • Routes of
    administration
    Topical (ointment)
    ATC code
    Legal status
    Legal status
    • UK: POM (Prescription only)
  • US: ℞-only
  • Pharmacokinetic data
    BioavailabilityLow
    Protein binding94%
    MetabolismHepatic, CYP3A4-mediated
    Elimination half-lifeUndetermined
    ExcretionUndetermined
    Identifiers
    • (3aS,4R,5S,6S,8R,9R,9aR,10R)-6-ethenyl-5-hydroxy-4,6,9,10-tetramethyl-1-oxodecahydro-3a,9-propano-3aH-cyclopenta[8]annulen-8-yl{[(1R,3s,5S)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl]sulfanyl}acetate

    CAS Number
    PubChem CID
    DrugBank
    ChemSpider
    UNII
    KEGG
    ChEMBL
    CompTox Dashboard (EPA)
    ECHA InfoCard100.167.142 Edit this at Wikidata
    Chemical and physical data
    FormulaC30H47NO4S
    Molar mass517.77 g·mol−1
    3D model (JSmol)
    • C[C@@H]1CC[C@@]23CCC(=O)[C@H]2[C@@]1([C@@H](C[C@@]([C@H]([C@@H]3C)O)(C)C=C)OC(=O)CS[C@@H]4C[C@H]5CC[C@@H](C4)N5C)C

    • InChI=1S/C30H47NO4S/c1-7-28(4)16-24(35-25(33)17-36-22-14-20-8-9-21(15-22)31(20)6)29(5)18(2)10-12-30(19(3)27(28)34)13-11-23(32)26(29)30/h7,18-22,24,26-27,34H,1,8-17H2,2-6H3/t18-,19+,20-,21+,22-,24-,26+,27+,28-,29+,30+/m1/s1 ☒N

    • Key:STZYTFJPGGDRJD-NHUWBDDWSA-N ☒N

     ☒NcheckY (what is this?)  (verify)

    Retapamulin is a topical antibiotic developed by GlaxoSmithKline. It is the first drug in the new class of pleuromutilin antibiotics to be approved for human use. It is marketed as an ointment under the brand names Altabax and Altargo.

    Retapamulin was approved by the United States Food and Drug Administration in April 2007 for the treatment of bacterial skin infections such as impetigo. In May 2007, retapamulin received approval in the EU from the European Medicines Agency for the same indication.[citation needed]

    Clinical trials have demonstrated its efficacy against certain Gram-positive bacteria including MRSA.[1]

    Indications[edit]

    Retapamulin is indicated for the topical treatment of impetigo due to Staphylococcus aureus (methicillin-susceptible only) or Streptococcus pyogenes.[2]

    Pharmacology[edit]

    Mechanism of action[edit]

    Retapamulin is an antibacterial agent, specifically a protein synthesis inhibitor. The medication selectively inhibits bacterial protein synthesis by interacting at a site on the 50S subunit of the bacterial ribosome through an interaction that differs from other antibiotics.[2]

    Pharmacokinetics[edit]

    Systemic exposure following topical application through intact skin is low.[2]

    Contraindications[edit]

    None yet reported.[2]

    Adverse reactions[edit]

    The most common reported adverse reaction was irritation at the application site.[2]

    References[edit]

    1. ^ Jones R, Fritsche T, Sader H, Ross J (2006). "Activity of retapamulin (SB-275833), a novel pleuromutilin, against selected resistant gram-positive cocci". Antimicrob Agents Chemother. 50 (7): 2583–6. doi:10.1128/AAC.01432-05. PMC 1489758. PMID 16801451.
  • ^ a b c d e Borrza, S.; Philippi, E., eds. (2007). Physicians' Desk Reference (62nd ed.). pp. 1318–20. ISBN 978-1-56363-660-8.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Retapamulin&oldid=1190969834"

    Categories: 
    Pleuromutilin antibiotics
    Drugs developed by GSK plc
    Secondary alcohols
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    This page was last edited on 20 December 2023, at 21:41 (UTC).

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