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MilliporeSigma

M7694

Sigma-Aldrich

Mupirocin

≥92% (HPLC), powder

Sinónimos:

5,9-Anhydro-2,3,4,8-tetradeoxy-8-[[3-(2-hydroxy-1-methylpropyl)oxiranyl]methyl]-3-methyl-[2E,8[2S,3S(1S,2S)]]-L-talonon-2-enonic acid 8-carboxyoctyl ester, BRL 4910A, Pseudomonic acid

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50 MG
$411.35
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$780.00

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50 MG
$411.35
100 MG
$780.00

About This Item

Fórmula empírica (notación de Hill):
C26H44O9
Número de CAS:
Peso molecular:
500.62
Número MDL:
Código UNSPSC:
12352200
ID de la sustancia en PubChem:
NACRES:
NA.77

$411.35

Precio de catálogo$433.00

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Nivel de calidad

Ensayo

≥92% (HPLC)

Formulario

powder

actividad óptica

[α]/D -15.7 to -20°, c = 1 in methanol

color

white to tan

solubilidad

DMSO: ≥10 mg/mL

espectro de actividad antibiótica

fungi

Modo de acción

enzyme | inhibits
protein synthesis | interferes

emisor

GlaxoSmithKline

temp. de almacenamiento

room temp

cadena SMILES

[H][C@@]1(CO[C@@H](C\C(C)=C\C(=O)OCCCCCCCCC(O)=O)[C@H](O)[C@@H]1O)C[C@@H]2O[C@@]2([H])[C@@H](C)[C@H](C)O

InChI

1S/C26H44O9/c1-16(13-23(30)33-11-9-7-5-4-6-8-10-22(28)29)12-20-25(32)24(31)19(15-34-20)14-21-26(35-21)17(2)18(3)27/h13,17-21,24-27,31-32H,4-12,14-15H2,1-3H3,(H,28,29)/b16-13+/t17-,18-,19-,20-,21-,24+,25-,26-/m0/s1

Clave InChI

MINDHVHHQZYEEK-HBBNESRFSA-N

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Descripción general

Mupirocin is produced by Pseudomonas fluorescens. Mupirocin is used to treat impetigo and skin infections.[1]

Aplicación

Mupirocin has been used:
  • for kinetic assay[2]
  • to assess its resistance by performing turbidity assay[3][4]
  • to determine its antimicrobial susceptibility[5]

Acciones bioquímicas o fisiológicas

Antibiotic; inhibits isoleucyl-tRNA synthetase (IRS).

Características y beneficios

This compound was developed by GlaxoSmithKline. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Nota de preparación

Mupirocin is poorly soluble in water (26 mg/L), but highly soluble in DMSO (≥10 mg/mL). If sterilization is required, it is advisable to use filter sterilization with a 0.22 µm PTFE, Polypropylene, or Nylon filter membrane.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)


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Jacobsen F, et al.
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Evaluation of the pig-tailed macaque (Macaca nemestrina) as a model of human Staphylococcus aureus nasal carriage
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Infection and Immunity, 86(6), e00043-e00018 (2018)
Gaston H M Vondenhoff et al.
European journal of medicinal chemistry, 46(11), 5227-5236 (2011-10-05)
Increasing resistance to antibiotics is a major problem worldwide and provides the stimulus for development of new bacterial inhibitors with preferably different modes of action. In search for new leads, several new bacterial targets are being exploited beside the use

Artículos

Bifidobacteria-selective media detects beneficial bacteria, aiding quality control in microbiology labs.

Bioactive small molecules for immune system signaling target identification/validation and antibiotics, antivirals, and antifungals offered.

Questions

  1. Can this antibiotic be autoclaved?

    1 answer
    1. The heat stability of Mupirocin has not been tested. It is poorly soluble in water (26 mg/L), but highly soluble in DMSO (≥10 mg/mL). Should sterilization be necessary, filter sterilization using a 0.22 um PTFE, Polypropylene, or Nylon filter membrane is recommended. One publication does suggest that this compound may be autoclaved, however this has not been validated.

      See the link below for a publication that may be helpful:
      https://citeseerx.ist.psu.edu/document?repid=rep1&type=pdf&doi=04422266ee0024deeab81bd939305cbb1e2bc261

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