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RET V804M-IN-1

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Catalog No. T8467Cas No. 2414909-94-5
Alias RETV804M kinase inhibitor, LUN09945

RET V804M-IN-1 (RETV804M kinase inhibitor) is a wt-RET -selective RETV804M kinase inhibitors(IC50 = 20 nM).

RET V804M-IN-1

RET V804M-IN-1

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Purity: 99.62%
Catalog No. T8467Alias RETV804M kinase inhibitor, LUN09945Cas No. 2414909-94-5
RET V804M-IN-1 (RETV804M kinase inhibitor) is a wt-RET -selective RETV804M kinase inhibitors(IC50 = 20 nM).
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$32In StockIn Stock
2 mg$45In StockIn Stock
5 mg$72In StockIn Stock
10 mg$97In StockIn Stock
25 mg$168In StockIn Stock
50 mg$263In StockIn Stock
100 mg$372In StockIn Stock
200 mg$549In StockIn Stock
1 mL x 10 mM (in DMSO)$79In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.62%
Appearance:Solid
Color:White
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Product Introduction

RET V804M-IN-1 AI Summary
RET V804M-IN-1 exhibits bioactivities related to the inhibition of the recombinant human RET V804M mutant, with an IC50 value of 51.0 nM in a TR-FRET assay. It demonstrates significant selectivity towards the RET V804M mutant over other targets, indicated by selectivity index ratios of 13.0 against human RET and 19.0 against human KDR, both in expression systems. Additionally, the compound shows efficacy in inhibiting the RET V804M mutant expressed in human BaF3 cells, with an IC50 value of 3900.0 nM in a cell viability assay. The selectivity towards RET V804M over wild-type RET and KDR in these cells is highlighted by selectivity index ratios of 0.85 and 1.9, respectively..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
RET V804M-IN-1 (RETV804M kinase inhibitor) is a wt-RET -selective RETV804M kinase inhibitors(IC50 = 20 nM).
Targets&IC50
RET (V804M):20 nM
SynonymsRETV804M kinase inhibitor, LUN09945
Chemical Properties
Molecular Weight344.37
FormulaC19H16N6O
Cas No.2414909-94-5
SmilesNC(=O)c1ccc(cc1)-c1cnn2ccc(NCc3cccnc3)nc12
Relative Density.1.38 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: 120 mg/mL (348.46 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 4 mg/mL (11.62 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 mM2.9039 mL14.5193 mL29.0385 mL145.1927 mL
5 mM0.5808 mL2.9039 mL5.8077 mL29.0385 mL
10 mM0.2904 mL1.4519 mL2.9039 mL14.5193 mL
20 mM0.1452 mL0.7260 mL1.4519 mL7.2596 mL
50 mM0.0581 mL0.2904 mL0.5808 mL2.9039 mL
100 mM0.0290 mL0.1452 mL0.2904 mL1.4519 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
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Dose Conversion

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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

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