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MDL 19301

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Catalog No. T11981Cas No. 89388-38-5

MDL 19301 is a nonsteroidal anti-inflammatory agent.

MDL 19301

MDL 19301

Copy Product Info
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Catalog No. T11981Cas No. 89388-38-5
MDL 19301 is a nonsteroidal anti-inflammatory agent.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mgInquiry3-6 months3-6 months
50 mgInquiry3-6 months3-6 months
100 mgInquiry3-6 months3-6 months
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction

Bioactivity
Description
MDL 19301 is a nonsteroidal anti-inflammatory agent.
In vivo
MDL 19301 exhibits additional anti-inflammatory effects by inhibiting carrageenan pleurisy, adjuvant arthritis, and HOAc-induced writhing. Pharmacologically, it suppresses prostaglandin synthesis, blocks arachidonic acid-induced diarrhea (excluding prostaglandin-E2-caused), and prevents arachidonic-acid-stimulated rat platelet aggregation (excluding ADP-induced). Contrary to expectations, both MDL 19301 and MDL 16,861 show minimal antipyretic effects in rats. Remarkably, oral MDL 19301 administration reduces rat paw edema significantly, induced either by carrageenan (ED30=4.8 mg/kg) or an Arthus reaction (ED30=8.2 mg/kg p.o.), and does not cause gastric ulceration in fasted rats at doses up to 1,000 mg/kg, indicating a better therapeutic index than traditional non-steroidal anti-inflammatory drugs (NSAIDs). The anti-inflammatory effect of MDL 19301 (unlike MDL 16,861) diminishes with SKF525A co-administration, suggesting MDL 19301's prodrug status for MDL 16,861 and its lower ulcerogenic potential.
Chemical Properties
Molecular Weight279.46
FormulaC15H21NS2
Cas No.89388-38-5
SmilesN(=C1SCCS1)C2=CC=C(C=C2)CCCCCC
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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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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