Antibacterial agent 357
Antibacterial agent 357 is an Antibacterial agent. Antibacterial agent 357 disrupts bacterial cell membranes, induces ROS accumulation, and triggers metabolic disorders. Antibacterial agent 357 exhibits antibacterial activity against MRSA, Staphylococcus aureus, and Gram-negative bacteria. Antibacterial agent 357 can be used in research related to MRSA infections, S. aureus infections, and Gram-negative bacterial infections.
For research use only. We do not sell to patients.
- Formula: C36H80Cl4N6O4
- Molecular Weight:802.87
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Antibacterial agent 357 (Compound 7d) (18 h) potently inhibits the growth of Staphylococcus aureus ATCC 29213, Enterococcus faecalis ATCC 29212, Escherichia coli ATCC 25922, Stenotrophomonas maltophilia ATCC 17808, MRSA isolates and Gram-negative isolates, with MIC values ranging from 0.5 to 4 μg/mL. Meanwhile, this agent exhibits low hemolytic toxicity (HC50 > 320 μg/mL) and a selectivity index > 640[1].
Antibacterial agent 357 (1-16 μg/mL) dose-dependently inhibits biofilm formation of S. aureus ATCC 29213 and disrupts pre-formed mature biofilms; at a concentration of 16 μg/mL, it reduces the survival rate of bacteria within the biofilm to <0.04%[1].
Antibacterial agent 357 (0.125-16 μg/mL; 10 mM NAC) exerts bactericidal activity against Staphylococcus aureus ATCC 29213 by disrupting bacterial cell membranes (targeting phosphatidylglycerol), inducing ROS accumulation, and causing morphological damage[1].
Antibacterial agent 357 alters the gene expression of S. aureus ATCC 29213, upregulating stress response pathways associated with membrane modification while downregulating pathways involved in protein synthesis and energy metabolism, which confirms its mechanism of action involving membrane disruption, ROS accumulation and metabolic disorder[1].
Antibacterial agent 357 (0.5-8 μg/mL; 24 h) exhibits favorable in vitro safety against GES cells, with a CC50 of 18.3 μg/mL. The cell survival rate exceeds 80% at the concentration of 8 μg/mL, and no significant membrane damage is observed[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Kunming mice (female, ~25 g, SPF)[1]
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Dosage:5 mg/kg/d; 10 mg/kg/d
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Administration:s.c.; every 12 hours; 6 total doses
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Result:Reduced bacterial load in mouse wound tissues at 5 mg/kg/d.
Exhibited potent antibacterial effects comparable to vancomycin at 10 mg/kg/d.
Significantly reduced subcutaneous inflammatory cell infiltration relative to untreated mice at both doses.
Chemical Information
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Molecular Weight 802.87
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Formula C36H80Cl4N6O4
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SMILES
[NH3+]CCCC[C@H]([NH3+])C(N(CCCCCCCCC)CCOCCOCCN(CCCCCCCCC)C([C@@H]([NH3+])CCCC[NH3+])=O)=O.[Cl-].[Cl-].[Cl-].[Cl-]
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
- Antibacterial agent 357
- Antibacterial agent357
- Antibacterial agent-357
- Bacterial
- Reactive Oxygen Species (ROS)
- E. faecalis ATCC 29212
- S. maltophilia ATCC 17808
- E. coli ATCC 25922
- reactive oxygen species
- human GES cells
- MRSA
- murine subcutaneous infection model
- Staphylococcus aureus
- Gram-negative bacteria
- S. aureus ATCC 29213
- Inhibitor
- inhibitor
- inhibit