Bacitracin, potency min. 60 Units/mg
Bacitracin, potency min. 60 Units/mg
Bacitracin, potency min. 60 Units/mg
Bacitracin, potency min. 60 Units/mg
Thermo Scientific Chemicals

Bacitracin, potency min. 60 Units/mg

Bacitracin, CAS # 1405-87-4, is cyclic polypeptide-based antibiotic which exhibits activity against microbes causing pneumonia, skin, and eye infections.
製品番号(カタログ番号)数量パッケージ
2261000505 gGlass Bottle
22610025025 gGlass Bottle
製品番号(カタログ番号) 226100050
価格(JPY)
-
見積もりを依頼する
数量:
5 g
パッケージ:
Glass Bottle
一括またはカスタム形式をリクエストする
化学物質識別子
CAS1405-87-4
IUPAC Name4-(2-{[2-(1-amino-2-methylbutyl)-4,5-dihydro-1,3-thiazol-4-yl]formamido}-4-methylpentanamido)-4-[(1-{[18-(3-aminopropyl)-12-benzyl-15-(butan-2-yl)-3-(carbamoylmethyl)-6-(carboxymethyl)-9-[(4H-imidazol-4-yl)methyl]-2,5,8,11,14,17,20-heptaoxo-1,4,7,10,13,16,19-heptaazacyclopentacosan-21-yl]carbamoyl}-2-methylbutyl)carbamoyl]butanoic acid zinc
Molecular FormulaC66H103N17O16SZn
InChI KeyQSNOBVJFKSQBBD-UHFFFAOYNA-N
SMILES[Zn].CCC(C)C(N)C1=NC(CS1)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(C(C)CC)C(=O)NC1CCCCNC(=O)C(CC(N)=O)NC(=O)C(CC(O)=O)NC(=O)C(CC2C=NC=N2)NC(=O)C(CC2=CC=CC=C2)NC(=O)C(NC(=O)C(CCCN)NC1=O)C(C)CC
さらに表示
Sulfated ash=<1.0 %
Composition>=40 % (Bacitracin A)
Composition>=70 % (sum of Bacitracin A, B1, B2 and B3)
Appearance (Color)White to yellow to beige
Appearance (Form)Powder
さらに表示
This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

General Description

• Bacitracin is a mixture of at least nine different cyclic polypeptides, originally isolated from Bacillus bacteria in 1945

• Bacitracins work by binding divalent metal cations and preventing the hydrolysis of lipids into usable cell wall components

Applications

• Bacitracin has been paired with nanoparticles in some laboratory studies to increase its effectivity

• It is suitable for the laboratory study of bacterial resistance, infection, and cross-reactivity

RUO – Research Use Only

Literature References

Tay, W.M.; Epperson, J.D.; da Silva, G.F.; Ming, L.J. 1H NMR, mechanism, and mononuclear oxidative activity of the antibiotic metallopeptide bacitracin: the role of D-Glu-4, interaction with pyrophosphate moiety, DNA binding and cleavage, and bioactivity. J Am Chem Soc. 2010, 28, 132(16), 5652-61.

Karala, A.R.; Ruddock, L.W. Bacitracin is not a specific inhibitor of protein disulfide isomerase. FEBS J. 2010, 277(11), 2454-62.