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TP-064

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Catalog No. T28996Cas No. 2080306-20-1
Alias TP 064

TP-064 is a potent and selective PRMT4 inhibitor, featuring an IC50 < 10nM for methylation of H3 (1-25) and over 100-fold selectivity compared to other histone methyltransferases and non-epigenetic targets. It inhibits the methylation of MED12 in cells with an IC50 of 43 nM.

TP-064

TP-064

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Purity: 97.85%
Catalog No. T28996Alias TP 064Cas No. 2080306-20-1
TP-064 is a potent and selective PRMT4 inhibitor, featuring an IC50 < 10nM for methylation of H3 (1-25) and over 100-fold selectivity compared to other histone methyltransferases and non-epigenetic targets. It inhibits the methylation of MED12 in cells with an IC50 of 43 nM.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$32In StockIn Stock
2 mg$45In StockIn Stock
5 mg$72In StockIn Stock
10 mg$122In StockIn Stock
25 mg$257In StockIn Stock
50 mg$513In StockIn Stock
100 mg$748-In Stock
1 mL x 10 mM (in DMSO)$73In StockIn Stock
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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.
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Purity:97.85%
Appearance:Solid
Color:Yellow
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Product Introduction

TP-064 AI Summary
TP-064 exhibits varying effects on cell viability across different cell types, including U2OS, human fibroblast, and HEK293T, showing both increases and decreases in growth rates. Its bioactivity may involve modulation of cellular functions related to viability and proliferation. Thermal Shift Assay results indicate that TP-064 affects the thermal stability of various protein domains, with decreases in stability noted in domains N44-E168, M626-G740, and M26-R383, and increases in stability observed in domains S229-K512, M1-L298, M1-K294, P449-E759, M1-S360, and G861-E979. Additionally, TP-064 potently inhibits FLAG-tagged CARM1 with an IC50 value of less than 10.0 nM, likely by disrupting the enzymatic activity through interaction with the substrate or necessary cofactors. This suggests TP-064's role in modulating both cellular viability mechanisms and protein stability..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
TP-064 is a potent and selective PRMT4 inhibitor, featuring an IC50 < 10nM for methylation of H3 (1-25) and over 100-fold selectivity compared to other histone methyltransferases and non-epigenetic targets. It inhibits the methylation of MED12 in cells with an IC50 of 43 nM.
Targets&IC50
MED12:43 nM(IC50), BAF155:340 nM(IC50), PRMT6:1300 μM, PRMT4:<10 nM
SynonymsTP 064
Chemical Properties
Molecular Weight458.6
FormulaC28H34N4O2
Cas No.2080306-20-1
SmilesCNCCN1CCC(CC1)c1cc(CN(C)C(=O)c2cccc(Oc3ccccc3)c2)ccn1
Relative Density.1.134 g/cm3 (Predicted)
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 50 mg/mL (109.03 mM), Sonication and heating to 60℃ are recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 4 mg/mL (8.72 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 mM2.1805 mL10.9027 mL21.8055 mL109.0275 mL
5 mM0.4361 mL2.1805 mL4.3611 mL21.8055 mL
10 mM0.2181 mL1.0903 mL2.1805 mL10.9027 mL
20 mM0.1090 mL0.5451 mL1.0903 mL5.4514 mL
50 mM0.0436 mL0.2181 mL0.4361 mL2.1805 mL
100 mM0.0218 mL0.1090 mL0.2181 mL1.0903 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

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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