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VRT-325

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Catalog No. T35074Cas No. 815592-21-3
Alias VRT-534, VRT325, VRT 325, CFcor-325, CFcor325, CFcor 325, CF-106951

VRT-325 can repair folding defects by promoting dimerization of the two NBDs or by promoting folding of the TMD.VRT-325 accelerates the healing rate of CF cell monolayers.

VRT-325

VRT-325

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Purity: 99.58%
Catalog No. T35074Alias VRT-534, VRT325, VRT 325, CFcor-325, CFcor325, CFcor 325, CF-106951Cas No. 815592-21-3
VRT-325 can repair folding defects by promoting dimerization of the two NBDs or by promoting folding of the TMD.VRT-325 accelerates the healing rate of CF cell monolayers.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$350In StockIn Stock
5 mg$970In StockIn Stock
10 mg$1,200In StockIn Stock
25 mg$1,590In StockIn Stock
50 mg$1,980-In Stock
100 mg$2,500-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
This molecule is a custom-made product. TargetMol has an excellent synthesis team with the experience and capability to provide you with cost-effective products.If you have any questions, please feel free to contact us. We are committed to serving you wholeheartedly.
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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Batch Information

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Purity:99.58%
Appearance:Solid
Color:White
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Product Introduction

VRT-325 AI Summary
VRT-325 exhibits corrector activity on the CFTR F508 deletion mutant expressed in various cell models, including human FRT cells, human CFBE41o cells, and mouse NIH/3T3 cells. In human FRT cells, it shows an Emax of 92.9% and an EC50 of 2200.0 nM after 25 minutes of incubation with forskolin, assessed by YFP-based fluorescence. In human CFBE41o cells, the compound demonstrates an EC50 of 2187.76 nM after preincubation for 24 hours followed by 30 minutes of stimulation with forskolin and genistein, evaluated using a fluorescence assay. In mouse NIH/3T3 cells, it has an EC50 of 3300.0 nM in a DiSBAC2 dye-based FRET assay, which includes preincubation for 16 hours before forskolin and genistein addition. Additionally, VRT-325 has a solubility of 1000.0 nM in a 50 mM ammonium acetate buffer at pH 7.4 after 24 hours and demonstrates a metabolic stability of 13.0%, as assessed by recombinant human CYP3A4-mediated drug degradation..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
VRT-325 can repair folding defects by promoting dimerization of the two NBDs or by promoting folding of the TMD.VRT-325 accelerates the healing rate of CF cell monolayers.
SynonymsVRT-534, VRT325, VRT 325, CFcor-325, CFcor325, CFcor 325, CF-106951
Chemical Properties
Molecular Weight510.65
FormulaC27H34N4O4S
Cas No.815592-21-3
SmilesO(C=1C2=C(N=C(C(C)N3CCN(S(=O)(=O)C4=CC=C(OC)C=C4)CC3)N1)C=CC=C2)C5CCCCC5
Relative Density.1.268 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 45 mg/mL (88.12 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.9583 mL9.7914 mL19.5829 mL97.9144 mL
5 mM0.3917 mL1.9583 mL3.9166 mL19.5829 mL
10 mM0.1958 mL0.9791 mL1.9583 mL9.7914 mL
20 mM0.0979 mL0.4896 mL0.9791 mL4.8957 mL
50 mM0.0392 mL0.1958 mL0.3917 mL1.9583 mL

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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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