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MG 149

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Catalog No. T6584Cas No. 1243583-85-8
Alias Tip60 HAT inhibitor, MG149

MG 149 (Tip60 HAT inhibitor) is a selective and potent Tip60 inhibitor with IC50 of 74 uM, similar potentcy for MOF(IC50= 47 uM).

MG 149

MG 149

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Purity: 99.86%
Catalog No. T6584Alias Tip60 HAT inhibitor, MG149Cas No. 1243583-85-8
MG 149 (Tip60 HAT inhibitor) is a selective and potent Tip60 inhibitor with IC50 of 74 uM, similar potentcy for MOF(IC50= 47 uM).
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$48In StockIn Stock
2 mg$68In StockIn Stock
5 mg$97In StockIn Stock
10 mg$179In StockIn Stock
25 mg$342In StockIn Stock
50 mg$546In StockIn Stock
100 mg$787-In Stock
1 mL x 10 mM (in DMSO)$116In 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:99.86%
Color:White
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Product Introduction

MG 149 AI Summary
MG 149 exhibits a broad range of bioactivities, prominently related to the inhibition of various histone acetyltransferases (HATs) including Tip60, PCAF, and p300 HAT domains. It competitively inhibits Tip60 with a Kis value of 54.0 µM and uncompetitively with a Kii value of 78.0 µM, effectively inhibiting Tip60-mediated histone acetylation in HeLa nuclear extracts, particularly impacting histone H3 and H4 acetylation with inhibition percentages exceeding 50.0%. Additionally, it inhibits the human His-tagged MOF enzyme with 100% inhibition at concentrations of 50 µM and 100 µM and shows IC50 values of 15000.0 nM and 27000.0 nM in respective radioactive acetylation and alphascreen assays. Beyond its activity in epigenetic regulation, MG 149 demonstrates potent bioactivity in various cell proliferation assays, cell lines including Plasmodium falciparum and ATL, as well as antagonism of the NFkB signaling pathway and cytotoxicity counterscreen, with potency in the nanomolar range. It also exhibits the ability to activate potato 5-lipoxygenase, evidenced by a fold change (FC) value of 3.0 at a 50 µM concentration. Moreover, it inhibits human COX2 with less than 50% inhibition using arachidonic acid as a substrate. Overall, MG 149 targets multiple biological pathways, suggesting potential as a versatile modulator of both epigenetic and cellular processes..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
MG 149 (Tip60 HAT inhibitor) is a selective and potent Tip60 inhibitor with IC50 of 74 uM, similar potentcy for MOF(IC50= 47 uM).
Targets&IC50
Tip60:74 μM, MOF:47 μM
SynonymsTip60 HAT inhibitor, MG149
Chemical Properties
Molecular Weight340.46
FormulaC22H28O3
Cas No.1243583-85-8
SmilesCCCCCCCc1ccc(CCc2cccc(O)c2C(O)=O)cc1
Relative Density.1.100 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
Ethanol: 63 mg/mL (185.04 mM), Sonication is recommended.
H2O: < 1 mg/mL (insoluble or slightly soluble)
DMSO: 255 mg/mL (748.99 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (5.87 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
Ethanol/DMSO
1mg5mg10mg50mg
1 mM2.9372 mL14.6860 mL29.3720 mL146.8601 mL
5 mM0.5874 mL2.9372 mL5.8744 mL29.3720 mL
10 mM0.2937 mL1.4686 mL2.9372 mL14.6860 mL
20 mM0.1469 mL0.7343 mL1.4686 mL7.3430 mL
50 mM0.0587 mL0.2937 mL0.5874 mL2.9372 mL
100 mM0.0294 mL0.1469 mL0.2937 mL1.4686 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:
mg/kg
g
μL
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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