Colistin sodium methanesulfonate

SIGMA/27655 - from Bacillus colistinus

Synonym: Colimycin sodium methanesulfonate; Methanesulfonic acid derivative of Polymyxin E; Polymyxin E sodium methanesulfonate

CAS Number: 8068-28-8
Empirical Formula (Hill Notation): C₅₈H₁₁₅N₁₆Na₅O₂₈S₅
Molecular Weight: 1759.90
EC Number: 232-516-9
MDL Number: MFCD00130824
Linear Formula: C₅₈H₁₁₅N₁₆Na₅O₂₈S₅
Product Type: Chemical

Catalog Number	PKG Qty.	Price


45-27655-1G	1 g	$182.00 1/EAAdd To Favorites	Add To Favorites
45-27655-5G	5 g	$768.00 1/EAAdd To Favorites	Add To Favorites

antibiotic activity spectrum	Gram-negative bacteria
biological source	Bacillus colistinus
color	white to off-white
form	powder or crystals
ign. residue	~20%
InChI	1S/C53H100N16O13.5CH4O3S.5Na/c1-9-30(6)12-10-11-13-41(72)60-33(14-20-54)48(77)69-43(32(8)71)53(82)65-36(17-23-57)45(74)64-38-19-25-59-52(81)42(31(7)70)68-49(78)37(18-24-58)62-44(73)34(15-21-55)63-50(79)39(26-28(2)3)67-51(80)40(27-29(4)5)66-46(75)35(16-22-56)61-47(38)76;51-5(2,3)4;;;;;/h28-40,42-43,70-71H,9-27,54-58H2,1-8H3,(H,59,81)(H,60,72)(H,61,76)(H,62,73)(H,63,79)(H,64,74)(H,65,82)(H,66,75)(H,67,80)(H,68,78)(H,69,77);51H3,(H,2,3,4);;;;;/q;;;;;;5*+1/p-5/t30?,31-,32-,33+,34-,35+,36+,37+,38+,39+,40-,42+,43+;;;;;;;;;;/m1........../s1
InChI key	WSDSONZFNWDYGZ-BKFDUBCBSA-I
loss	≤5.0% loss on drying
mode of action	cell membrane \| interferes
pH	6.5-8.5
Quality Level	200
SMILES string	[Na+].[Na+].[Na+].[Na+].[Na+].CS([O-])(=O)=O.CS([O-])(=O)=O.CS([O-])(=O)=O.CS([O-])(=O)=O.CS([O-])(=O)=O.CCC(C)CCCCC(=O)N[C@@H](CCN)C(=O)N[C@@H](C(C)O)C(=O)N[C@@H](CCN)C(=O)N[C@H]1CCNC(=O)[C@@H](NC(=O)[C@H](CCN)NC(=O)[C@@H](CCN)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](CCN)NC1=O)C(C)O
storage temp.	2-8°C

Application:	Colistin sodium methanesulfate is used to permeabilize bacterial cell membranes and to study mannose-resistant haemagglutination.
Biochem/physiol Actions:	Colistin sodium methanesulfate is a cyclopolypeptide antibiotic with endotoxin-binding capacity Colistin′s activity stems from the hydrophobic and hydrophillic regions. They solubilze the cytoplasmic membrane which contributes to the bactericidal effect .
Biochem/physiol Actions:	Mode of Action: Binds to lipids on the cell cytoplasmic membrane of Gram-negative bacteria and disrupts the cell wall integrity. Antimicrobial spectrum: Gram-negative bacteria.
General description:	Chemical structure: peptide
Other Notes:	Keep container tightly closed in a dry and well-ventilated place. Keep in a dry place. Keep in a dry place.
Packaging:	1g, 5g

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	51102829