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Classification | API >> Antibiotics >> Other antibiotics |
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Name | Polymyxin B sulfate |
Synonyms | Aerosporin; N-[3-Amino-1-[[1-[[3-amino-1-[[6,9,18-tris(2-aminoethyl)-15-benzyl-3-(1-hydroxyethyl)-12-(2-methylpropyl)-2,5,8,11,14,17,20-heptaoxo-1,4,7,10,13,16,19-heptazacyclotricos-21-yl]carbamoyl]propyl]carbamoyl]-2-hydroxy-propyl]carbamoyl]propyl]-6-methyl-octanamide sulfuric acid |
Molecular Structure | ![]() |
Molecular Formula | C56H98N16O13.H2SO4 |
Molecular Weight | 1301.56 |
CAS Registry Number | 1405-20-5 |
EC Number | 215-774-7 |
SMILES | CCC(C)CCCCC(=O)NC(CCN)C(=O)NC(C(C)O)C(=O)NC(CCN)C(=O)NC1CCNC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC1=O)CCN)CC2=CC=CC=C2)CC(C)C)CCN)CCN)C(C)O.OS(=O)(=O)O |
Hazard Symbols |
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Hazard Statements | H302 Details | ||||||||||||||||||||
Precautionary Statements | P264-P270-P301+P317-P330-P501 Details | ||||||||||||||||||||
Hazard Classification | |||||||||||||||||||||
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SDS | Available | ||||||||||||||||||||
Polymyxin B sulfate, a potent antibiotic, was discovered in the 1940s by researchers at the University of Michigan and subsequently developed for clinical use. It is derived from the bacterium Bacillus polymyxa, which produces a group of polypeptide antibiotics known as polymyxins. Polymyxin B was identified as one of the most effective members of this antibiotic group against gram-negative bacteria. Its discovery marked a significant advancement in the treatment of bacterial infections, particularly those caused by multidrug-resistant pathogens. Polymyxin B sulfate is primarily used for the treatment of infections caused by multidrug-resistant gram-negative bacteria, including Pseudomonas aeruginosa, Acinetobacter baumannii, and Klebsiella pneumoniae. These bacteria are notorious for their resistance to multiple antibiotics, making polymyxin B a crucial therapeutic option. Polymyxin B is often employed in the management of ventilator-associated pneumonia (VAP) caused by multidrug-resistant gram-negative pathogens. VAP is a serious complication in patients receiving mechanical ventilation, and polymyxin B's activity against these resistant bacteria makes it a valuable choice in the treatment of this life-threatening infection. In cases of complicated urinary tract infections (cUTI) and catheter-associated urinary tract infections (CAUTI) caused by multidrug-resistant gram-negative bacteria, polymyxin B sulfate is often considered as a last-line treatment option. Its ability to penetrate the urinary tract and exert bactericidal activity against these pathogens makes it an important therapeutic agent in urological infections. Polymyxin B sulfate is also available in topical formulations for the treatment of skin and soft tissue infections caused by susceptible gram-negative bacteria. It is often combined with other antibiotics, such as bacitracin and neomycin, in over-the-counter ointments and creams for the management of minor wounds, cuts, and abrasions. |
Market Analysis Reports |
List of Reports Available for Polymyxin B sulfate |