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Polymyxin B sulfate salt

SIAL/P1004

Synonym: Polymixin; Polymixin B; Polymixin B sulfate

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-P1004-1MU 1000000 units
$55.90
1/EA
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45-P1004-5MU 5000000 units
$153.00
1/EA
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45-P1004-10MU 10000000 units
$237.00
1/EA
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45-P1004-25MU 25000000 units
$475.00
1/EA
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45-P1004-50MU 50000000 units
$817.00
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.

This image depicts SKU: P1004-50MU

 

antibiotic activity spectrum fungi
  Gram-negative bacteria
biological source Pseudomonas aeruginosa
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
solubility water: 50 mg/mL
storage condition (Tightly closed. Dry. )
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.
Application: Polymyxin B sulfate salt has been used:
•  in human aortic endothelial cells (HAEC) cell culture to exclude potential endotoxin contamination in recombinant adiponectin
•  in the analysis of the isolates
•  in endotoxin-neutralizing activity of α-amylase (AmyI-1)-18 (LAL assay)

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.
Biochem/physiol Actions: Polymyxin B is one of the most important antibiotics used to treat gram-negative bacterial infections, including infections caused by carbapenem-resistant non-fermenters and carbapenem-resistant Enterobacteriaceae.
Features and Benefits: High quality antibiotic suitable for mulitple research applications
General description: 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.
Other Notes: For additional information on our range of Biochemicals , please complete this form .
Other Notes: Keep container tightly closed in a dry and well-ventilated place. Keep in a dry place.
Packaging: 1000000, 5000000, 10000000, 25000000, 50000000 units in poly bottle
Preparation Note: Polymyxin B sulfate is soluble in water at 50 mg/mL, producing a very slightly hazy, colorless to yellow solution. It has only minimal solubility in any organic solvent. For example, it has a solubility of 0.115 mg/mL in ethanol.

Stock solutions should be sterile filtered and stored at 2-8°C. They are stable at 37°C for 5 days.
Storage and Stability: 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.
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 51101500

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