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Polymyxin B sulfate

SIAL/P0972 - meets USP testing specifications

Synonym: Polymyxin B sulfate salt

CAS Number: 1405-20-5
Empirical Formula (Hill Notation): C55H96N16O13 · 2H2SO4
Molecular Weight: 1385.61
EC Number: 215-774-7
MDL Number: MFCD00131991
Linear Formula: C55H96N16O13 · 2H2SO4
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-P0972-1MU 1000000 units
$83.10
1/EA
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45-P0972-10MU 10000000 units
$412.00
1/EA
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45-P0972-50MU 50000000 units
$1460.00
1/EA
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agency meets USP testing specifications
  USP/NF
antibiotic activity spectrum fungi
  Gram-negative bacteria
  Gram-positive bacteria
application(s) pharmaceutical (small molecule)
form powder
InChI 1S/C48H82N16O13.H2O4S/c1-27(2)24-37-47(76)59-32(11-19-52)41(70)56-31(10-18-51)43(72)61-35(14-22-65)39(68)54-21-13-34(45(74)57-33(12-20-53)44(73)64-38(48(77)63-37)25-28-6-4-3-5-7-28)60-42(71)30(9-17-50)58-46(75)36(15-23-66)62-40(69)29(8-16-49)55-26-67;1-5(2,3)4/h3-7,26-27,29-38,65-66H,8-25,49-53H2,1-2H3,(H,54,68)(H,55,67)(H,56,70)(H,57,74)(H,58,75)(H,59,76)(H,60,71)(H,61,72)(H,62,69)(H,63,77)(H,64,73);(H2,1,2,3,4)
InChI key HNDFYNOVSOOGDU-UHFFFAOYSA-N
mode of action cell membrane | interferes
Quality Level 200 
SMILES string O=C(C(NC(C(CCN)NC(CCCCC(C)CC)=O)=O)C(C)O)NC(CCN)C(NC(CCNC(C(NC(C(NC(C(CCN)N1)=O)CCN)=O)C(O)C)=O)C(NC(CCN)C(NC(CC2=CC=CC=C2)C(NC(CC(C)C)C1=O)=O)=O)=O)=O.O=S(O)(O)=O
storage temp. 2-8°C
Application: Polymyxin B sulfate is a strongly cationic cyclic polypeptide antibiotic that is derived from fermentation of Bacilus polymyxa. It is a mixture of B1 and B2 sulfate. The product has been used clinically to treat infections of the urinary tract, meninges and blood stream caused by susceptible strains of Pseudomonas aeruginosa. It also has uses studying multidrug-resistant pathogens, as an immobilized agent for removal of endotoxins, and to induce pore formation in the membranes of cortex cells from excised sorghum roots.
Biochem/physiol Actions: Mode of Action: Polymyxin B Sulfate binds to the lipid A portion of bacterial lipopolysaccharides†, disrupting the cytoplasmic membrane by inducing pores large enough to permit nucleotide leakage in bacterial walls. This disrupts the permeability of the cytoplasmic membrane.

Antimicrobial spectrum: Has bactericidal action on most gram-negative bacilli††, including E. Coli and on most fungi and gram-positive bacteria.
Caution: As supplied, the product should be stored at 2-8°C in the dark. No change was observed in retained samples after three years′ of storage in these conditions. Stock solutions should be sterile filtered and stored at 2-8°C. They are stable at 37°C for 5 days.
General description: Chemical structure: peptide
Packaging: This product is packaged in a bottomless glass bottle, with its contents inside an inserted fused cone.
Symbol GHS07  GHS07
Signal word Warning
Hazard statements H302
Precautionary statements P264 - P270 - P301 + P312 - P501
Hazard Codes Xn
Risk Statements 22
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Storage Temp. 2-8°C
UNSPSC 12352209

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