M7694
Mupirocin
≥92% (HPLC), powder
Synonym(s):
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
About This Item
Recommended Products
Quality Level
assay
≥92% (HPLC)
form
powder
optical activity
[α]/D -15.7 to -20°, c = 1 in methanol
color
white to tan
solubility
DMSO: ≥10 mg/mL
antibiotic activity spectrum
fungi
mode of action
enzyme | inhibits
protein synthesis | interferes
originator
GlaxoSmithKline
storage temp.
room temp
SMILES string
[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
InChI key
MINDHVHHQZYEEK-HBBNESRFSA-N
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General description
Application
- for kinetic assay
- to assess its resistance by performing turbidity assay
- to determine its antimicrobial susceptibility
Biochem/physiol Actions
Features and Benefits
Preparation Note
Storage Class
11 - Combustible Solids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Certificates of Analysis (COA)
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