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Vanzacaftor

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Catalog No. T74417Cas No. 2374124-49-7
Alias VX-121, VX121

Vanzacaftor is a cystic fibrosis transmembrane conductance regulator (CFTR) modulator designed to improve CFTR protein processing and trafficking to the cell surface. Vanzacaftor enhances CFTR functionality, restoring chloride transport, and serves as a critical research tool for the development of therapies targeting cystic fibrosis.

Vanzacaftor

Vanzacaftor

😃Good
Purity: 99.14%
Catalog No. T74417Alias VX-121, VX121Cas No. 2374124-49-7
Vanzacaftor is a cystic fibrosis transmembrane conductance regulator (CFTR) modulator designed to improve CFTR protein processing and trafficking to the cell surface. Vanzacaftor enhances CFTR functionality, restoring chloride transport, and serves as a critical research tool for the development of therapies targeting cystic fibrosis.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$196In StockIn Stock
5 mg$359In StockIn Stock
10 mg$533In StockIn Stock
25 mg$786In StockIn Stock
50 mg$1,190In StockIn Stock
100 mg$1,830-In Stock
1 mL x 10 mM (in DMSO)$489In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
With extensive experience in compound synthesis, we can provide rapid custom synthesis services for this product according to your research needs.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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Purity:99.14%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Vanzacaftor is a cystic fibrosis transmembrane conductance regulator (CFTR) modulator designed to improve CFTR protein processing and trafficking to the cell surface. Vanzacaftor enhances CFTR functionality, restoring chloride transport, and serves as a critical research tool for the development of therapies targeting cystic fibrosis.
In vitro
When the concentration of Vanzacaftor was 0-10 μM, it stimulated K⁺ secretion in Homo sapiens bronchial epithelial cells (HBEs) at low micromolar concentrations, with an EC₅₀ value of 4.4 μM for this effect being inhibited by Paxilline [2].
Treatment with 1 μM, 5 μM, and 10 μM Vanzacaftor significantly enhanced the αBKCa current in HEK cells, and this current could be blocked by Paxilline [2].
When 5 μM Vanzacaftor acted on hippocampal primary neurons, it reduced their action potential discharge frequency and altered neuronal excitability [2].
SynonymsVX-121, VX121
Chemical Properties
Molecular Weight617.76
FormulaC32H39N7O4S
Cas No.2374124-49-7
SmilesC(COC1=NN(C=C1)C=2N=C3N4C(C)(C)C[C@@](C4)(CCCN=C5NC(S(=O)(=O)NC(=O)C3=CC2)=CC=C5)[H])C6C7(C68CC8)CC7
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: 80 mg/mL (129.5 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+90% Corn Oil: 3.3 mg/mL (5.34 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.6188 mL8.0938 mL16.1875 mL80.9376 mL
5 mM0.3238 mL1.6188 mL3.2375 mL16.1875 mL
10 mM0.1619 mL0.8094 mL1.6188 mL8.0938 mL
20 mM0.0809 mL0.4047 mL0.8094 mL4.0469 mL
50 mM0.0324 mL0.1619 mL0.3238 mL1.6188 mL
100 mM0.0162 mL0.0809 mL0.1619 mL0.8094 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:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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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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