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Amtolmetin guacil

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Catalog No. T19672Cas No. 87344-06-7
Alias ST-679, ST679, ST 679, MED-15, MED15, MED 15

Amtolmetin guacil (ST-679) inhibits prostaglandin synthesis and cyclooxygenase. Amtolmetin guacil has similar NSAID properties like tolmetin with additional analgesic, antipyretic, and gastroprotective properties.

Amtolmetin guacil

Amtolmetin guacil

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🥰Excellent
Purity: 99.85%
Catalog No. T19672Alias ST-679, ST679, ST 679, MED-15, MED15, MED 15Cas No. 87344-06-7
Amtolmetin guacil (ST-679) inhibits prostaglandin synthesis and cyclooxygenase. Amtolmetin guacil has similar NSAID properties like tolmetin with additional analgesic, antipyretic, and gastroprotective properties.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$31In StockIn Stock
25 mg$68In StockIn Stock
50 mg$100In StockIn Stock
100 mg$148In StockIn Stock
500 mg$329In StockIn Stock
1 mL x 10 mM (in DMSO)$29In StockIn 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.
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Purity:99.85%
Appearance:Solid
Color:White
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Product Introduction

Amtolmetin guacil AI Summary
Amtolmetin guacil inhibits the production of nitric oxide (NO) induced by LPS/IFNgamma in mouse RAW264.7 cells, with an IC50 value of 51300.0 nM determined by the Griess reagent method after 24 hours of treatment. It also exhibits antiviral activity, inhibiting SARS-CoV-2 induced cytotoxicity in various cell lines. Specifically, it inhibits cytotoxicity of Caco-2 cells at 10 µM after 48 hours with 0.41% inhibition, and VERO-6 cells at the same concentration and duration with -0.05% inhibition. Additionally, Amtolmetin guacil inhibits the SARS-CoV-2 3CL-Pro protease by 7.964% at 20 µM. This compound also shows inhibitory effects on human HDAC6 enzyme activity, with 27.41% inhibition using a commercial peptide substrate, but exhibits a -1.33% inhibition when a custom peptide substrate is used, suggesting variability in its efficacy depending on the assay conditions..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Amtolmetin guacil (ST-679) inhibits prostaglandin synthesis and cyclooxygenase. Amtolmetin guacil has similar NSAID properties like tolmetin with additional analgesic, antipyretic, and gastroprotective properties.
SynonymsST-679, ST679, ST 679, MED-15, MED15, MED 15
Chemical Properties
Molecular Weight420.46
FormulaC24H24N2O5
Cas No.87344-06-7
SmilesCOc1ccccc1OC(=O)CNC(=O)Cc1ccc(C(=O)c2ccc(C)cc2)n1C
Relative Density.1.19 g/cm3
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: 60 mg/mL (142.7 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+90% Corn Oil: 2.5 mg/mL (5.95 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 mM2.3783 mL11.8917 mL23.7835 mL118.9174 mL
5 mM0.4757 mL2.3783 mL4.7567 mL23.7835 mL
10 mM0.2378 mL1.1892 mL2.3783 mL11.8917 mL
20 mM0.1189 mL0.5946 mL1.1892 mL5.9459 mL
50 mM0.0476 mL0.2378 mL0.4757 mL2.3783 mL
100 mM0.0238 mL0.1189 mL0.2378 mL1.1892 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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