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Colistin Methanesulfonate (sodium salt)

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    Colistin Methane<wbr/>sulfonate (sodium salt)
  • Colistin Methane<wbr/>sulfonate (sodium salt)
Cat No: 17180
Cayman

Colistin methanesulfonate is a prodrug for colistin (also known as polymyxin E), an antibiotic that is effective against most Gram-negative bacteria but suffers from nephro- and neurotoxicity.{28077,22080} Colistin methanesulfonate is used against inf...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • colistimethate, pentasodium salt
Correlated keywords:
  • 1867-68-1 2680-63-9 8068-37-9 11033-40-2 11048-71-8 12676-33-4 12768-67-1 21362-08-3 37196-55-7 155704-91-9 3061-80-1 27010-23-7 biochemical infectious disease colistinemthanesulfonic acid colimycin M colistimethate sulfomethate methyl sulfate sodium salt colistinat coly-mycin coly mycin injectable promixin E W-1929 prodrug gram negative bacteria W1929 antibiotic multidrug resistant drug
Product Overview:
Colistin methanesulfonate is a prodrug for colistin (also known as polymyxin E), an antibiotic that is effective against most Gram-negative bacteria but suffers from nephro- and neurotoxicity.{28077,22080} Colistin methanesulfonate is used against infections caused by multidrug resistant Gram-negative bacteria, alone or in combination with other antibiotics.{28077}
Size 1 g
Shipping wet ice
CAS Number 8068-28-8
Molecular Formula C58H105N16O28S5 • 5Na (for Colistin A)
SMILES CC[C@H](CCCCC(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H]1CCNC([C@H]([C@H](O)C)NC([C@@H](NC([C@@H](NC([C@@H](NC([C@H](NC([C@@H](NC1=O)CCNCS([O-])(=O)=O)=O)CC(C)C)=O)CC(C)C)=O)CCNCS([O-])(=O)=O)=O)CCNCS([O-])(=O)=O)=O)=O)=O)CCNCS([O-])(=O)=O)=O)[C@H](O)C)=O)CCNCS([O
Molecular Weight 1749,8
Formulation A crystalline solid
Custom Code 2922.19
UNSPSC code 12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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