Mupirocine, > = 92% ( HPLC), poudre

Name: Mupirocine, > = 92% ( HPLC), poudre
Brand: SIGMA-ALDRICH
SKU: m7694-100mg
Price: 883.11 USD

Code: m7694-100mg D2-231

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Mupirocin has been used:for kinetic assayto assess its resistance by performing turbidity assayto determine its antimicrobial susceptibility

Biochem...

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$883.11 100MG

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Non disponible en dehors du Royaume-Uni et de l'Irlande
Application
Mupirocin has been used:for kinetic assayto assess its resistance by performing turbidity assayto determine its antimicrobial susceptibility
Biochem/physiol Actions
Antibiotic; inhibits isoleucyl-tRNA synthetase (IRS).
Features and Benefits
This compound was developed by GlaxoSmithKline. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.
General description
Mupirocin is produced by Pseudomonas fluorescens. It exhibits bacteriostatic action. Mupirocin is used to treat impetigo and skin infections.
Packaging
50, 100 mg in glass bottle

antibiotic activity spectrum fungi
assay ≥92% (HPLC)
color white to tan
form powder
InChI key MINDHVHHQZYEEK-HBBNESRFSA-N
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
mode of action protein synthesis | interferes, enzyme | inhibits
optical activity [α]/D -15.7 to -20°, c = 1 in methanol
originator GlaxoSmithKline
Quality Level 100
SMILES string [H][C@@]1(CO[C@@H](CC(C)=CC(=O)OCCCCCCCCC(O)=O)[C@H](O)[C@@H]1O)C[C@@H]2O[C@@]2([H])[C@@H](C)[C@H](C)O
solubility DMSO: ≥10 mg/mL
storage temp. room temp

Fiche de données de sécurité
Safety Data Sheet for M7694-100MG
Certificat d'analyse
Certificat d'analyse Sigma

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Cas Number 12650-69-0

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Mupirocine, > = 92% ( HPLC), poudre

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antibiotic activity spectrum	fungi
assay	≥92% (HPLC)
color	white to tan
form	powder
InChI key	MINDHVHHQZYEEK-HBBNESRFSA-N
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
mode of action	protein synthesis \| interferes, enzyme \| inhibits
optical activity	[α]/D -15.7 to -20°, c = 1 in methanol
originator	GlaxoSmithKline
Quality Level	100
SMILES string	[H][C@@]1(CO[C@@H](CC(C)=CC(=O)OCCCCCCCCC(O)=O)[C@H](O)[C@@H]1O)C[C@@H]2O[C@@]2([H])[C@@H](C)[C@H](C)O
solubility	DMSO: ≥10 mg/mL
storage temp.	room temp