| Field | Specification |
|---|---|
| Alternative names | Meclofenamate sodium |
| CAS no. | |
| Applications | |
| Source | Endogenous metabolite |
| Molecular weight | |
| Molecular formula | C14H10Cl2NNaO2 |
| Purity | |
| SMILES | |
| Form | Solid |
| Storage | |
| Shipping | |
| Catalog no. (Mfr.) | |
| Main SKU |
Compound Overview
Meclofenamic acid sodium, also known as Meclofenamate sodium, is a non-steroidal anti-inflammatory agent (NSAID). It is a non-selective gap-junction blocker and a highly selective inhibitor of the fat- and obesity-related enzyme (FTO). It has anti-inflammatory and antitumor activities[1][2][3]. It is supplied as a white to off-white solid (C14H10Cl2NNaO2, MW 318.13) at 99.89% purity.
Physical & Chemical Properties
| CAS Number | 6385-02-0 |
|---|---|
| Molecular Formula | C14H10Cl2NNaO2 |
| Molecular Weight | 318.13 g/mol |
| Purity | 99.89% |
| Appearance | Solid |
| Color | White to off-white |
| Structure Classification | Ketones, Aldehydes, Acids |
| SMILES | O=C(O[Na])C1=CC=CC=C1NC2=C(Cl)C=CC(C)=C2Cl |
| Signaling Pathway | Cytoskeleton; Metabolic Enzyme/Protease |
| Initial Source | Endogenous metabolite |
| Solubility | In Vitro: H2O: 100 mg/mL (314.34 mM; Requires sonication) DMSO: 100 mg/mL (314.34 mM; Requires sonication; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO) |
| Storage | 4°C, sealed storage, away from moisture and light. In solvent: -80°C, 1 year; -20°C, 6 months (sealed storage, away from moisture and light). |
| Shipping | Room temperature in continental US; may vary elsewhere. |
Literature Cited
Sources cited in this description and in the In Vitro & In Vivo Data tab. Peer-reviewed publications that used this product are listed under References.
Safety
For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with the Safety Data Sheet and your institution's chemical hygiene plan.
In Vitro
| Solvent | Solubility | Notes |
|---|---|---|
| H2O | 100 mg/mL (314.34 mM) | requires sonication |
| DMSO | 100 mg/mL (314.34 mM) | requires sonication; use freshly opened DMSO (absorbed moisture lowers solubility) |
Aliquot the stock solution and store it at -80°C (up to 1 year) or -20°C (up to 6 months); sealed storage, away from moisture and light; avoid repeated freeze-thaw cycles.
If water is used as the stock solvent, dilute to the working solution and sterilize it through a 0.22 μm filter before use.
In Vivo
Choose the formulation that suits the animal model and route of administration; percentages are volume ratios of the final working solution. Start from a clear DMSO stock (see In Vitro above), add the co-solvents one at a time in the order listed, mixing after each addition, and prepare the working solution fresh on the day of dosing. If precipitation or phase separation occurs, gentle warming or sonication can help.
Protocol 1
| Composition | 10% DMSO + 40% PEG300 + 5% Tween-80 + 45% saline |
|---|---|
| Result | ≥ 2.08 mg/mL (6.54 mM); clear solution |
| How to prepare | Gives a clear solution at ≥ 2.08 mg/mL (saturation not determined). For 1 mL of working solution: add 100 μL DMSO stock (20.8 mg/mL) to 400 μL PEG300; then 50 μL Tween-80; then 450 μL saline to bring the volume to 1 mL. Saline: dissolve 0.9 g sodium chloride in ddH2O and make up to 100 mL. |
Protocol 2
| Composition | 10% DMSO + 90% (20% SBE-β-CD in saline) |
|---|---|
| Result | ≥ 2.08 mg/mL (6.54 mM); clear solution |
| How to prepare | Gives a clear solution at ≥ 2.08 mg/mL (saturation not determined). For 1 mL of working solution: add 100 μL DMSO stock (20.8 mg/mL) to 900 μL 20% SBE-β-CD in saline. 20% SBE-β-CD in saline: dissolve 2 g SBE-β-CD powder in 10 mL saline until clear (4°C, store up to one week). |
Protocol 3
| Composition | 10% DMSO + 90% Corn Oil |
|---|---|
| Result | ≥ 2.08 mg/mL (6.54 mM); clear solution |
| How to prepare | Gives a clear solution at ≥ 2.08 mg/mL (saturation not determined). Use with caution if continuous dosing will exceed two weeks. For 1 mL of working solution: add 100 μL DMSO stock (20.8 mg/mL) to 900 μL corn oil. |
Data provided by the manufacturer.
In Vitro
Meclofenamic acid sodium (10, 100, 200 mM, 4 days) suppresses haSMC proliferation and migration[1]. In combination with gefitinib, Meclofenamic acid sodium (4, 6 μM, 48 h) induces caspase-related apoptosis in resistant NSCLC cells[2].
Cell Cycle Analysis[1]
| Cell Line | haSMCs |
|---|---|
| Concentration | 10, 100, 200 mM |
| Incubation Time | 4 days |
| Result | Caused a G2/M-phase block |
Western Blot Analysis[1]
| Cell Line | haSMCs |
|---|---|
| Concentration | 10, 100, 200 mM |
| Incubation Time | 4 days |
| Result | Decreased the expression of p44/42 MAPK. |
In Vivo
In a mouse prostate tumor model, Meclofenamic acid sodium (10 mg/kg/day, injected intraperitoneally for 20 days) displays antitumor activity[2].
| Animal Model | Prostate tumor model in mice[2] |
|---|---|
| Dosage | 10 mg/kg |
| Administration | i.p. |
| Result | Decreased tumor aggression, increased fibrosis, cellular proliferation and vascularity reduction. |
Data provided by the manufacturer. Numbered citations refer to the Literature Cited list in the product description.
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