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name9-[(E)-4-[(2S,3R,4R,5S)-3,4-dihydroxy-5-[ [(2S,3S)-3-[(2S,3S)-3-hydroxybutan-2-yl]oxiran-2-yl]methyl]oxan-2-yl]-3-methylbut-2-enoyl]oxynonanoic acidIdentifiersCAS number 12650-69-0ATC code D06AX09 R01AX06PubChem 446596Chemical dataFormula C26H44O9Mol. mass 500.622 g/molPharmacokinetic dataBioavailability ?Protein bactroban side effects 97%Metabolism.
in the bactroban side effects of methicillin-resistant Staphyolococcus aureus (MRSA), which is simply called Mupirocin Ointment.[2] MupirocinFrom Wikipedia, the free encyclopedia(Redirected from Bactroban)Jump to: navigation, searchMupirocinSystematic (IUPAC) name9-[(E)-4-[(2S,3R,4R,5S)-3,4-dihydroxy-5-[ [(2S,3S)-3-[(2S,3S)-3-hydroxybutan-2-yl]oxiran-2-yl]methyl]oxan-2-yl]-3-methylbut-2-enoyl]oxynonanoic bactroban side effects number 12650-69-0ATC code D06AX09 R01AX06PubChem 446596Chemical dataFormula C26H44O9Mol. mass bactroban side effects g/molPharmacokinetic dataBioavailability ?Protein binding 97%Metabolism ?Half life bactroban side effects to 40 minutesExcretion ?Therapeutic considerationsPregnancy cat. ?Legal statusRoutes ?Mupirocin (pseudomonic acid A, or Bactroban or Centany) is an bactroban side effects originally isolated from Pseudomonas fluorescens. It is used topically, and is primarily effective against Gram-positive bacteria. Mupirocin is bacteriostatic at low concentrations and bactericidal at high concentrations.[1]Contents.
is bacteriostatic at low concentrations and bactericidal at high concentrations.[1]Contents [hide]1 Mechanism2 Uses3 Sources4.
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