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SIRT6-IN-5

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Catalog No. T24793Cas No. 891002-11-2
Alias SIRT6 inhibitor-5, SIRT6 inhibitor5, SIRT6 inhibitor 5, SIRT6 IN 5

SIRT6-IN-5(SIRT6 inhibitor 5) is a potent and selective SIRT6 inhibitor with an IC50 value of 34 μM.SIRT6-IN-5 is immunosuppressive and chemo-sensitizing, increases H3K9 acetylation and glucose uptake in cultured cells, and reduces T-cell proliferation.

SIRT6-IN-5

SIRT6-IN-5

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Purity: 98.77%
Catalog No. T24793Alias SIRT6 inhibitor-5, SIRT6 inhibitor5, SIRT6 inhibitor 5, SIRT6 IN 5Cas No. 891002-11-2
SIRT6-IN-5(SIRT6 inhibitor 5) is a potent and selective SIRT6 inhibitor with an IC50 value of 34 μM.SIRT6-IN-5 is immunosuppressive and chemo-sensitizing, increases H3K9 acetylation and glucose uptake in cultured cells, and reduces T-cell proliferation.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$51In StockIn Stock
5 mg$122In StockIn Stock
10 mg$197In StockIn Stock
25 mg$397In StockIn Stock
50 mg$788In StockIn Stock
100 mg$1,070In StockIn Stock
500 mg$2,130-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:98.77%
Appearance:Solid
Color:White
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Product Introduction

SIRT6-IN-5 AI Summary
SIRT6-IN-5 shows potent inhibition of SIRT6 with 100% inhibition at 200µM and an IC50 value of 34000nM. It also inhibits SIRT1 and SIRT2 with IC50 values of 783000nM and 453000nM, respectively, giving selectivity indices of 23.02 and 13.32 for SIRT1 and SIRT2 relative to SIRT6. In human BxPC3 cells, SIRT6-IN-5 increases H3K9 acetylation, enhances glucose uptake, and inhibits TNFalpha production. The compound has a pKa of 2.58, a logP of 2.6, and moderate aqueous solubility. It has low fractions unbound in human and mouse plasma. The pharmacokinetic parameters in ICR mice include AUC, MRT, half-life, Tmax, and Cmax..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
SIRT6-IN-5(SIRT6 inhibitor 5) is a potent and selective SIRT6 inhibitor with an IC50 value of 34 μM.SIRT6-IN-5 is immunosuppressive and chemo-sensitizing, increases H3K9 acetylation and glucose uptake in cultured cells, and reduces T-cell proliferation.
Targets&IC50
SIRT6:34 μM
SynonymsSIRT6 inhibitor-5, SIRT6 inhibitor5, SIRT6 inhibitor 5, SIRT6 IN 5
Chemical Properties
Molecular Weight366.32
FormulaC19H14N2O6
Cas No.891002-11-2
SmilesN(C(=O)C1=CC=C(NC(=O)C2=CC=CO2)C=C1)C3=CC(C(O)=O)=C(O)C=C3
Relative Density.1.520 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: 55 mg/mL (150.14 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.7299 mL13.6493 mL27.2985 mL136.4927 mL
5 mM0.5460 mL2.7299 mL5.4597 mL27.2985 mL
10 mM0.2730 mL1.3649 mL2.7299 mL13.6493 mL
20 mM0.1365 mL0.6825 mL1.3649 mL6.8246 mL
50 mM0.0546 mL0.2730 mL0.5460 mL2.7299 mL
100 mM0.0273 mL0.1365 mL0.2730 mL1.3649 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:
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