Shopping Cart
Remove All
  • TargetMol
    Your shopping cart is currently empty

TP0427736

Copy Product Info
😃Good
Catalog No. T24897Cas No. 864374-00-5
Alias TP-427736, TP427736, TP-0427736

TP0427736 is a potent and selective inhibitor of ALK5 with an IC50 of 2.72 nM, 300-fold higher than the inhibitory effect on ALK3. TP0427736 reduces TGF-β-induced growth inhibition in human outer root sheath cells and elongates the anagen phase in mouse hair follicles.

TP0427736

TP0427736

Copy Product Info
😃Good
Purity: 97.26%
Catalog No. T24897Alias TP-427736, TP427736, TP-0427736Cas No. 864374-00-5
TP0427736 is a potent and selective inhibitor of ALK5 with an IC50 of 2.72 nM, 300-fold higher than the inhibitory effect on ALK3. TP0427736 reduces TGF-β-induced growth inhibition in human outer root sheath cells and elongates the anagen phase in mouse hair follicles.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$97In StockIn Stock
5 mg$238In StockIn Stock
10 mg$389In StockIn Stock
25 mg$663In StockIn Stock
50 mg$945-In Stock
1 mL x 10 mM (in DMSO)$269In StockIn Stock
Add to Cart
Add to Quotation
In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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.
Questions
TargetMol
View More

Batch Information

Select Batch
Purity:97.26%
Contact us for more batch information

Resource Download

Product Introduction

TP0427736 AI Summary
TP0427736 has demonstrated significant bioactivity, including a high solubility of 14,900.0 µg/mL. It acts as an inhibitor in various assays with notable potency: it inhibits ALK5-mediated TNFalpha-induced Smad2/3 phosphorylation with an IC50 of 8.7 nM, and it inhibits human ALK5 using GST-tagged Smad3 as a substrate with an IC50 of 2.7 nM. Additionally, it inhibits human GST-tagged TGFbeta 1 using 3,3',5,5'-tetramethylbenzidine as a substrate, with an IC50 of 2.72 nM when incubated for 30 minutes in the presence of ATP. Moreover, it shows inhibitory activity against human GST-tagged ALK3 with an IC50 value of 836.0 nM, also following a 30-minute incubation with ATP by the QSSA Kit method..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
TP0427736 is a potent and selective inhibitor of ALK5 with an IC50 of 2.72 nM, 300-fold higher than the inhibitory effect on ALK3. TP0427736 reduces TGF-β-induced growth inhibition in human outer root sheath cells and elongates the anagen phase in mouse hair follicles.
Targets&IC50
ALK5:2.72 nM
SynonymsTP-427736, TP427736, TP-0427736
Chemical Properties
Molecular Weight298.39
FormulaC14H10N4S2
Cas No.864374-00-5
SmilesCC=1N=C(C2=C(NC=N2)C=3C=C4C(=CC3)N=CS4)SC1
Relative Density.1.439 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: 65 mg/mL (217.84 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.3513 mL16.7566 mL33.5132 mL167.5659 mL
5 mM0.6703 mL3.3513 mL6.7026 mL33.5132 mL
10 mM0.3351 mL1.6757 mL3.3513 mL16.7566 mL
20 mM0.1676 mL0.8378 mL1.6757 mL8.3783 mL
50 mM0.0670 mL0.3351 mL0.6703 mL3.3513 mL
100 mM0.0335 mL0.1676 mL0.3351 mL1.6757 mL

Calculator

  • Molarity Calculator
  • Dilution Calculator
  • Reconstitution Calculator
  • Molecular Weight Calculator

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:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

You can also refer to dose conversion for different animals. More Dose Conversion

Tech Support

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

Keywords

Related Tags: buy TP0427736 | purchase TP0427736 | TP0427736 cost | order TP0427736 | TP0427736 chemical structure | TP0427736 formula | TP0427736 molecular weight