| Size | Price | Stock | Qty |
|---|---|---|---|
| 1mg |
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| Other Sizes |
| Targets |
Meloxicam D4 targets the same enzymes as its unlabeled parent drug. Meloxicam is a non-steroidal anti-inflammatory agent that inhibits COX activity, with IC50s of 0.49 µM and 36.6 µM for COX-2 and COX-1, respectively. By selectively inhibiting COX-2, it reduces the production of prostaglandins while minimizing gastrointestinal side effects.
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|---|---|
| ln Vitro |
Meloxicam D4 is primarily used as an analytical internal standard rather than for its pharmacological activity. Meloxicam is a non-steroidal anti-inflammatory agent (NSAID). The compound is used in LC-MS/MS methods for the quantification of Meloxicam in biological matrices. The deuterium labeling provides a mass shift for accurate quantification.
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| ln Vivo |
Meloxicam D4 is used in pharmacokinetic studies as an internal standard for the quantification of Meloxicam. Meloxicam is an NSAID used for its analgesic and anti-inflammatory effects. The deuterium-labeled compound can be co-administered with unlabeled Meloxicam to study absorption, distribution, metabolism, and excretion.
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| Enzyme Assay |
In vitro assays for Meloxicam D4 are typically performed as part of analytical method validation. The compound is used as an internal standard in LC-MS/MS assays for the quantification of Meloxicam. It is dissolved in an appropriate solvent and spiked into biological matrices at known concentrations. Calibration curves are generated by plotting the peak area ratio of Meloxicam to Meloxicam D4 against the concentration of Meloxicam.
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| Cell Assay |
For in vitro cell-based assays, Meloxicam D4 can be used in studies investigating Meloxicam's cellular effects, though its primary use is as an analytical internal standard. Cells are treated with the compound, and its effects on prostaglandin production are measured. However, due to its role as an internal standard, it is more frequently used in the analytical quantification of the parent drug.
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| Animal Protocol |
In vivo animal studies with Meloxicam D4 are primarily pharmacokinetic. The compound is administered orally to rodents, and blood samples are collected at predetermined time points. Plasma concentrations of both labeled and unlabeled Meloxicam are analyzed by LC-MS/MS using Meloxicam D4 as the internal standard. Pharmacodynamic effects can be evaluated in models of inflammation and pain.
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| ADME/Pharmacokinetics |
Meloxicam D4 (CAS: 942047-63-4) has a molecular weight of 354.42 g/mol and a molecular formula of C14H13N3O4S2. Appearance: solid powder. Purity: ≥98%. Storage: powder -20°C for 3 years, in solvent -80°C for 1 year. The compound is a deuterium-labeled internal standard for Meloxicam.
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| Toxicity/Toxicokinetics |
Meloxicam D4 is used in very small quantities as an analytical internal standard and does not pose significant toxicity risks under normal handling. As a deuterium-labeled analog of an approved NSAID, it is expected to have a similar pharmacological profile, but toxicology studies are typically not performed on the labeled compound. Meloxicam is generally well-tolerated.
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| References | |
| Additional Infomation |
Meloxicam D4 is a deuterium-labeled form of Meloxicam, a non-steroidal anti-inflammatory agent (NSAID). It has the CAS number 942047-63-4 and a molecular weight of 354.42 g/mol. It is intended for use as an internal standard for the quantification of Meloxicam. It is not intended for therapeutic use and is for research and analytical use only.
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| Molecular Formula |
C14H13N3O4S2
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|---|---|
| Molecular Weight |
354.41920542717
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| Exact Mass |
351.035
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| CAS # |
942047-63-4
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| Related CAS # |
Meloxicam;71125-38-7;Meloxicam sodium;71125-39-8
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| PubChem CID |
54682543
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| Appearance |
Light yellow to yellow solid powder
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| Melting Point |
249-251°C
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| LogP |
3.619
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| Hydrogen Bond Donor Count |
2
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| Hydrogen Bond Acceptor Count |
7
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| Rotatable Bond Count |
2
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| Heavy Atom Count |
23
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| Complexity |
628
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| Defined Atom Stereocenter Count |
0
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| SMILES |
[2H]C([2H])([2H])N1C(=C(C2=CC=CC=C2S1(=O)=O)O)C(=O)NC3=NC=C(S3)C
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| InChi Key |
ZRVUJXDFFKFLMG-BMSJAHLVSA-N
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| InChi Code |
InChI=1S/C14H13N3O4S2/c1-8-7-15-14(22-8)16-13(19)11-12(18)9-5-3-4-6-10(9)23(20,21)17(11)2/h3-7,18H,1-2H3,(H,15,16,19)/i2D3
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| Chemical Name |
4-hydroxy-N-(5-methyl-1,3-thiazol-2-yl)-1,1-dioxo-2-(trideuteriomethyl)-1λ6,2-benzothiazine-3-carboxamide
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| HS Tariff Code |
2934.99.9001
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| Storage |
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
| Shipping Condition |
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
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| Solubility (In Vitro) |
May dissolve in DMSO (in most cases), if not, try other solvents such as H2O, Ethanol, or DMF with a minute amount of products to avoid loss of samples
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|---|---|
| Solubility (In Vivo) |
Note: Listed below are some common formulations that may be used to formulate products with low water solubility (e.g. < 1 mg/mL), you may test these formulations using a minute amount of products to avoid loss of samples.
Injection Formulations
Injection Formulation 1: DMSO : Tween 80： Saline = 10 : 5 : 85 (i.e. 100 μL DMSO stock solution → 50 μL Tween 80 → 850 μL Saline)(e.g. IP/IV/IM/SC) *Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH ₂ O to obtain a clear solution. Injection Formulation 2: DMSO : PEG300 ：Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL DMSO → 400 μLPEG300 → 50 μL Tween 80 → 450 μL Saline) Injection Formulation 3: DMSO : Corn oil = 10 : 90 (i.e. 100 μL DMSO → 900 μL Corn oil) Example: Take the Injection Formulation 3 (DMSO : Corn oil = 10 : 90) as an example, if 1 mL of 2.5 mg/mL working solution is to be prepared, you can take 100 μL 25 mg/mL DMSO stock solution and add to 900 μL corn oil, mix well to obtain a clear or suspension solution (2.5 mg/mL, ready for use in animals). View More
Injection Formulation 4: DMSO : 20% SBE-β-CD in saline = 10 : 90 [i.e. 100 μL DMSO → 900 μL (20% SBE-β-CD in saline)] Oral Formulations
Oral Formulation 1: Suspend in 0.5% CMC Na (carboxymethylcellulose sodium) Oral Formulation 2: Suspend in 0.5% Carboxymethyl cellulose Example: Take the Oral Formulation 1 (Suspend in 0.5% CMC Na) as an example, if 100 mL of 2.5 mg/mL working solution is to be prepared, you can first prepare 0.5% CMC Na solution by measuring 0.5 g CMC Na and dissolve it in 100 mL ddH2O to obtain a clear solution; then add 250 mg of the product to 100 mL 0.5% CMC Na solution, to make the suspension solution (2.5 mg/mL, ready for use in animals). View More
Oral Formulation 3: Dissolved in PEG400 (Please use freshly prepared in vivo formulations for optimal results.) |
| Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
| 1 mM | 2.8215 mL | 14.1076 mL | 28.2151 mL | |
| 5 mM | 0.5643 mL | 2.8215 mL | 5.6430 mL | |
| 10 mM | 0.2822 mL | 1.4108 mL | 2.8215 mL |
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.
Calculation results
Working concentration： mg/mL；
Method for preparing DMSO stock solution： mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation:：Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O，mix and clarify.
(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
(2) Be sure to add the solvent(s) in order.
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