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Description
A benzamide ether derivative that exhibits potent bactericidal activity against Staphylococcus aureus and Bacillus subtilis (minimum inhibitory concentration = 0.5 to 1mg/ml), but does not affect E. coli , yeast, or human hepatocytes. Shown to reduce GTPase activity and induce FtsZ (a prokaryotic homologue of tubulin) polymerization in S. aureus in a dose-dependent manner. Reported to directly inhibit the GTPase activity of FtsZ in a concentration dependent manner (IC50 = 55 ng/ml). Shown to bind between the C-ternimal domain and helix 7 in a region analogous to the Taxol binding site of tubulin. Increases the survival rate to 100% in mice subjected to a lethal dose of S. aureus .
Specifications
Specifications
| Color | Tan |
| Description | 97% by HPLC |
| Target Proteins | FtsZ |
| Molecular Formula | C14H8ClF2N3O2S |
| Formula Weight | 355.8g/mol |
| Solubility | DMSO |
| Content And Storage | Protect from light |
| Form | Powder |
| Quantity | 5 mg |
Product Title
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