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Antibiofilm agent-17

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Catalog No. T211776

Antibiofilm agent-17 is a dual-action biofilm inhibitor (IC50 = 0.33 μM) targeting Pseudomonas aeruginosa. It inhibits biofilm growth by reducing virulence production regulated by the quorum sensing system and decreasing iron acquisition capability. In a mouse wound infection model, Antibiofilm agent-17 shows synergistic antibacterial activity. This compound is useful for research on combating Pseudomonas aeruginosa infections.

Antibiofilm agent-17

Antibiofilm agent-17

😃Good
Catalog No. T211776
Antibiofilm agent-17 is a dual-action biofilm inhibitor (IC50 = 0.33 μM) targeting Pseudomonas aeruginosa. It inhibits biofilm growth by reducing virulence production regulated by the quorum sensing system and decreasing iron acquisition capability. In a mouse wound infection model, Antibiofilm agent-17 shows synergistic antibacterial activity. This compound is useful for research on combating Pseudomonas aeruginosa infections.
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All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Product Introduction

Bioactivity
Description
Antibiofilm agent-17 is a dual-action biofilm inhibitor (IC50 = 0.33 μM) targeting Pseudomonas aeruginosa. It inhibits biofilm growth by reducing virulence production regulated by the quorum sensing system and decreasing iron acquisition capability. In a mouse wound infection model, Antibiofilm agent-17 shows synergistic antibacterial activity. This compound is useful for research on combating Pseudomonas aeruginosa infections.
In vitro
Antibiofilm agent-17 (Compound 19I) (0.0625-1 μM, 24 hours) acts against biofilm formation in Pseudomonas aeruginosa PAO1 by inhibiting the las and pqs systems, achieving up to 69.49% inhibition at 1 μM without affecting bacterial growth. It suppresses biofilm formation in PA0617, PA1065, PA1121, and PA1167 strains. By impeding the quorum sensing (QS) system, as well as clustering and swimming motility, it interferes with biofilm formation. Additionally, Antibiofilm agent-17 (0.0625-1 μM) enhances Pvd and Pch production, causing iron scarcity in bacteria, thereby inhibiting biofilm development. However, it does not affect biofilm formation in ΔpvdS and fpvA overexpressing strains. At 2.5-200 μM for 24 hours, it demonstrates no toxicity to mouse and rabbit erythrocytes, RAW264.7 cells, HepG2 cells, and Galleria mellonella larvae.
In vivo
Antibiofilm agent-17 (Compound 19I) at concentrations of 12.5-200 μM over a period of 0-120 hours does not affect the survival rate of zebrafish larvae. At a concentration of 1 μM, it enhances the survival rate of wax moth larvae infected with Pseudomonas aeruginosa PAO1 when treated with Tobramycin, Ciprofloxacin, Meropenem, and Polymyxin B (Polymyxin B). When applied to wound infections in mice at 1 μM, daily for 3 days, it accelerates wound healing when used in combination with Tobramycin and Ciprofloxacin.
Chemical Properties
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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