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Vanzacaftor

🥰Excellent
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

🥰Excellent
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$1,320In StockIn Stock
5 mg$2,650In StockIn Stock
10 mg$3,580In StockIn Stock
25 mg$5,320In StockIn Stock
50 mg$7,180In 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%
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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
ColorWhite
AppearanceSolid
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 recommeded.
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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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
All types of co-solvents required for the protocol, such asDMSO, PEG300/ PEG400, Tween 80, SBE-β-CD, corn oil are available for purchase on the TargetMol website with a simple click.
1 Enter information below:
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2 Enter the in vivo formulation:
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