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Corrector C4

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Catalog No. T31014Cas No. 421580-53-2
Alias Corrector C-4, Corrector C 4, Corr-4a, Corr4a, Corr 4a

Corrector C4, a corrector commonly used to study cystic fibrosis mutants, works by alleviating the interaction between CFTR transmembrane domain mutants and protein homeostasis.

Corrector C4

Corrector C4

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Purity: 99.98%
Catalog No. T31014Alias Corrector C-4, Corrector C 4, Corr-4a, Corr4a, Corr 4aCas No. 421580-53-2
Corrector C4, a corrector commonly used to study cystic fibrosis mutants, works by alleviating the interaction between CFTR transmembrane domain mutants and protein homeostasis.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$195In StockIn Stock
5 mg$483In StockIn Stock
10 mg$692In StockIn Stock
25 mg$1,080In StockIn Stock
50 mg$1,490In StockIn Stock
100 mg$1,970In StockIn Stock
500 mg$3,930-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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Purity:99.98%
Appearance:Solid
Color:Yellow
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Product Introduction

Corrector C4 AI Summary
Corrector C4 exhibits corrector activity on the human CFTR deltaF508 mutant expressed in FRT cells, evidenced by increases in iodide influx and YFP-based fluorescence analysis, with an EC50 value ranging from 1096.48 nM to 2300.0 nM. The compound shows a Vmax value of 122.0 microM/s and a Kd value of 900.0 nM, along with an IC50 value of 6000.0 nM for iodide influx assessed by fluorescence assay. Beyond its role as a CFTR corrector, Corrector C4 demonstrates a broad spectrum of bioactivities including modulation of Lamin A splicing, SMN2 splice variant expression, and inhibition of tau fibril formation, AMP beta-lactamase, ALDH1A1, Jumonji Domain Containing 2E, Cruzain, Menin-MLL interaction, HPGD, Eya2, Histone Lysine Methyltransferase G9a, BAZ2B, and TCP-1 ring complex. It exhibits anti-tumor efficacy in certain human colon tumor cells and shows potential against malarial parasite plastids with potencies ranging from 707.9 nM to 199526.2 nM across different assays. Its physicochemical properties include a Log P value of 5.96, a solubility of 20.0 nM, an apparent permeability of 8.1 x 10^-6 cm/s, and membrane retention of 37.9%. The compound maintains metabolic stability, with approximately 55% remaining after 1-hour incubation with CYP3A4 and a human plasma half-life of 86.6 hours. Additionally, it has a binding affinity to human serum albumin with a dissociation constant of 11680.0 nM and a Bmax of 88.82%. Corrector C4 is soluble in 50 mM ammonium acetate buffer at 250 μM and demonstrates efficacy in correcting defective trafficking of the CFTR protein with demonstrated activities in various cell lines upon pre-incubation and forskolin/genistein stimulation..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Corrector C4, a corrector commonly used to study cystic fibrosis mutants, works by alleviating the interaction between CFTR transmembrane domain mutants and protein homeostasis.
SynonymsCorrector C-4, Corrector C 4, Corr-4a, Corr4a, Corr 4a
Chemical Properties
Molecular Weight456.97
FormulaC21H17ClN4O2S2
Cas No.421580-53-2
SmilesCC1=C(C=2N=C(NC3=C(OC)C=CC(Cl)=C3)SC2)SC(NC(=O)C4=CC=CC=C4)=N1
Relative Density.1.440 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: 60 mg/mL (131.3 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.1883 mL10.9416 mL21.8833 mL109.4164 mL
5 mM0.4377 mL2.1883 mL4.3767 mL21.8833 mL
10 mM0.2188 mL1.0942 mL2.1883 mL10.9416 mL
20 mM0.1094 mL0.5471 mL1.0942 mL5.4708 mL
50 mM0.0438 mL0.2188 mL0.4377 mL2.1883 mL
100 mM0.0219 mL0.1094 mL0.2188 mL1.0942 mL

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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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