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JG26

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Catalog No. T27654Cas No. 1464910-32-4
Alias JG-26, JG 26

JG26 is a potent inhibitor of ADAM17, which can inhibit ADAM8, ADAM17, ADAM10 and MMP-12, with IC50 values of 12 nM, 1.9 nM, 150 nM and 9.4 nM, respectively, and can be used to study the immune system of the body.

JG26

JG26

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Purity: 99.08%
Catalog No. T27654Alias JG-26, JG 26Cas No. 1464910-32-4
JG26 is a potent inhibitor of ADAM17, which can inhibit ADAM8, ADAM17, ADAM10 and MMP-12, with IC50 values of 12 nM, 1.9 nM, 150 nM and 9.4 nM, respectively, and can be used to study the immune system of the body.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$83-In Stock
5 mg$198-In Stock
10 mg$297-In Stock
25 mg$523-In Stock
50 mgPreferential-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:99.08%
Appearance:Solid
Color:White
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Product Introduction

JG26 AI Summary
JG26 exhibits bioactivity as a potent inhibitor of ADAM-17, with IC50 values ranging from 1.9 nM to 4272.0 nM across different cell lines and induction methods. It demonstrates high selectivity for ADAM-17 over other metalloproteinases like MMP-14, MMP-9, and MMP-2, with selectivity ratios in IC50 values ranging from 126.0 to 10000.0. The compound also shows inhibitory activity against recombinant ADAM-10 (IC50 of 150.0 nM) and recombinant ADAM-8 (IC50 of 12.0 nM), and it inhibits the shedding of CD23 by ADAM-8 with an IC50 of 120.0 nM. Additionally, it inhibits MMP-1 in human rheumatoid synovial fibroblasts with an IC50 greater than 500000.0 nM, as well as MMP-2 (IC50 of 240.0 nM), MMP-9 (IC50 of 1630.0 nM), MMP-12 (IC50 of 9.4 nM), and MMP-14 catalytic domain (IC50 of 19500.0 nM). Furthermore, the compound exhibits a 59.87% activity in inhibiting cell invasion in human MDA-MB-231 cells as assessed using DAPI staining based confocal microscopy..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
JG26 is a potent inhibitor of ADAM17, which can inhibit ADAM8, ADAM17, ADAM10 and MMP-12, with IC50 values of 12 nM, 1.9 nM, 150 nM and 9.4 nM, respectively, and can be used to study the immune system of the body.
Targets&IC50
ADAM17:1.9 nM (IC50), MMP8:240 nM (IC50), MMP14:19500 nM (IC50), MMP12:9.4 nM (IC50), ADAM10:150 nM (IC50), MMP9:>500000 nM (IC50), MMP9:1630 nM (IC50), ADAM8:12 nM (IC50)
SynonymsJG-26, JG 26
Chemical Properties
Molecular Weight594.27
FormulaC19H22Br2N4O6S
Cas No.1464910-32-4
SmilesS(N[C@H](CCCNC(N)=O)C(NO)=O)(=O)(=O)C1=CC=C(OCC2=CC(Br)=CC(Br)=C2)C=C1
Relative Density.1.683 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: 50 mg/mL (84.14 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (3.37 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 mM1.6827 mL8.4137 mL16.8274 mL84.1368 mL
5 mM0.3365 mL1.6827 mL3.3655 mL16.8274 mL
10 mM0.1683 mL0.8414 mL1.6827 mL8.4137 mL
20 mM0.0841 mL0.4207 mL0.8414 mL4.2068 mL
50 mM0.0337 mL0.1683 mL0.3365 mL1.6827 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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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

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