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Meloxicam

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Catalog No. T0826Cas No. 71125-38-7
Alias Movalis, Mobic, Metacam

Meloxicam (Metacam) is a Nonsteroidal Anti-inflammatory Drug. The mechanism of action of meloxicam is as a Cyclooxygenase Inhibitor. The chemical classification of meloxicam is Nonsteroidal Anti-inflammatory Compounds.

Meloxicam

Meloxicam

😃Good
Purity: 99.60%
Catalog No. T0826Alias Movalis, Mobic, MetacamCas No. 71125-38-7
Meloxicam (Metacam) is a Nonsteroidal Anti-inflammatory Drug. The mechanism of action of meloxicam is as a Cyclooxygenase Inhibitor. The chemical classification of meloxicam is Nonsteroidal Anti-inflammatory Compounds.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
100 mg$33In StockIn Stock
200 mg$45In StockIn Stock
500 mg$83-In Stock
1 mL x 10 mM (in DMSO)$37In 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:99.60%
Appearance:Solid
Color:White to Yellow
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Product Introduction

Bioactivity
Description
Meloxicam (Metacam) is a Nonsteroidal Anti-inflammatory Drug. The mechanism of action of meloxicam is as a Cyclooxygenase Inhibitor. The chemical classification of meloxicam is Nonsteroidal Anti-inflammatory Compounds.
Targets&IC50
COX-2:0.49 µM, COX-1:36.6 µM
In vitro
In horses, administration of Meloxicam significantly reduced lameness at both 8 and 24 hours post-injection and showed a tendency to decrease exudation. Compared to placebo, Meloxicam markedly inhibited the release of prostaglandin E2 and substance P in the synovial fluid 8 hours post-injection and reduced bradykinin release at 24 hours. Additionally, Meloxicam decreased average matrix metalloproteinase activity in the equine system at both 8 and 24 hours post-administration. Horses treated with Meloxicam or phenylbutazone showed improved postoperative pain and clinical outcomes compared to those treated with saline solution (SS). Meloxicam also induced a substantial infiltration of neutrophils in ischemic lesion tissues in horses. In dogs, Meloxicam significantly reduced concentrations of prostaglandin E2 in the blood and synovial fluid on days 7 and 21 post-administration, with no significant effect on thromboxane B2 (TXB2) levels in the blood or prostaglandin E2 (PGE2) concentrations in the gastric mucosa. Furthermore, Meloxicam inhibited tumor growth and pulmonary metastasis of LM-8 cells in mice.
In vivo
Meloxicam induces apoptosis in MG-63 cell cultures, concurrently upregulating both Bax mRNA and protein levels. It significantly reduces colony size in HCA-7 and Moser-S cells. While it markedly inhibits colony formation and tumor growth in HCA-7 cells, Meloxicam shows no effect on the growth of COX-2 negative HCT-116 cells. Furthermore, Meloxicam suppresses PGE(2) production, proliferation, and invasiveness, particularly in MG-63 cells expressing relatively higher levels of COX-2.
SynonymsMovalis, Mobic, Metacam
Chemical Properties
Molecular Weight351.40
FormulaC14H13N3O4S2
Cas No.71125-38-7
SmilesCN1C(C(=O)NC2=NC=C(C)S2)=C(O)C2=CC=CC=C2S1(=O)=O
Relative Density.1.613 g/cm3 (Predicted)
Storage & Solubility Information
Storagestore at low temperature | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
Ethanol: < 1 mg/mL (insoluble or slightly soluble)
DMSO: 10.64 mg/mL (30.28 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 1 mg/mL (2.85 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 mM2.8458 mL14.2288 mL28.4576 mL142.2880 mL
5 mM0.5692 mL2.8458 mL5.6915 mL28.4576 mL
10 mM0.2846 mL1.4229 mL2.8458 mL14.2288 mL
20 mM0.1423 mL0.7114 mL1.4229 mL7.1144 mL

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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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