FtsZ-IN-1
FtsZ-IN-1 is a potent FtsZ inhibitor with quinolinium ring. FtsZ-IN-1 has stronger antibacterial activity against Gram-positive bacteria with MICs of 0.5-8 μg/mL. FtsZ-IN-1 significantly causes cell elongation of B. subtilis by enhancing FtsZ polymerization. FtsZ-IN-1 exhibits low hemolytic toxicity and low tendency to induce agent resistance. FtsZ-IN-1 has against drug-resistant bacteria activity.
For research use only. We do not sell to patients.
- CAS No.: 2516246-24-3
- Formula: C26H32IN3
- Molecular Weight:513.46
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
FtsZ[1]
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| HK-2 | IC50 |
9.42 μg/mL
Compound: A3
|
Cytotoxicity against human HK-2 cells incubated for 48 hrs by MTT assay
Cytotoxicity against human HK-2 cells incubated for 48 hrs by MTT assay
|
[PMID: 35421657] |
| L929 | IC50 |
12.77 μg/mL
Compound: A3
|
Cytotoxicity against mouse L929 cells incubated for 48 hrs by MTT assay
Cytotoxicity against mouse L929 cells incubated for 48 hrs by MTT assay
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[PMID: 35421657] |
FtsZ-IN-1 (compound A3) inhibits effectively the growth of S. aureus with MICs of 0.5-1 μg/mL, and generally displays less antibacterial potency against most Gram-negative bacteria tested such as E. coli ATCC 8739 (MIC = 64 μg/mL) and P. Aeruginosa ATCC 27853 (MIC >64 μg/mL)[1].
FtsZ-IN-1 exhibits MBCs of 4-8 μg/mL and MICs of 1-4 μg/mL against S. aureus, B. subtilis and E. faecium[1].
FtsZ-IN-1 (0-24 μg/mL; 24 hours) inhibits the growth of S. aureus in a bacteriostatic mode at 1×, 2×, 4× MIC concentrations, and kills S. aureus at 8× MIC concentration[1].
FtsZ-IN-1 can restore the antibacterial activity of methicillin against MRSA in a synergistic manner, with MIC of 2 μg/mL[1].
FtsZ-IN-1 (2 μg/mL; 4 hours) can enlarge cell size of B. subtilis and inhibits bacterial cell division[1].
FtsZ-IN-1 (0-15 μg/mL; 48 hours) exhibits IC50s of 12.77 and 9.42 μg/mL in L929 and HK-2 cells[1].
FtsZ-IN-1 (2 μg/mL) can effectively delay the induction of drug resistance[1].
In a Hemolytic activity assay, FtsZ-IN-1 (1-64 μg/mL; 1 hour) exhibits low hemolytic toxicity in mice erythrocytes (from Kunming mice) with IC5 of 64 μg/mL[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:L929 and HK-2 cells[1]
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Concentration:0-15 μg/mL
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Incubation Time:48 hours
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Result:Exhibited IC50s of 12.77 and 9.42 μg/mL in L929 and HK-2 cells.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 2516246-24-3
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Molecular Weight 513.46
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Formula C26H32IN3
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SMILES
CC1CCN(C2=C3C=CC=CC3=[N+](C)C(/C=C/C4=CC=C(N(C)C)C=C4)=C2)CC1.[I-]
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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)