Mefenamic acid
CAS No. 61-68-7
Mefenamic acid( C.I. 473 | NSC 94437 )
Catalog No. M15330 CAS No. 61-68-7
Mefenamic acid is a Nonsteroidal Anti-inflammatory Drug. The mechanism of action of mefenamic acid is as a Cyclooxygenase Inhibitor.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 200MG | 28 | In Stock |
|
| 500MG | 46 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameMefenamic acid
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NoteResearch use only, not for human use.
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Brief DescriptionMefenamic acid is a Nonsteroidal Anti-inflammatory Drug. The mechanism of action of mefenamic acid is as a Cyclooxygenase Inhibitor.
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DescriptionMefenamic acid is a Nonsteroidal Anti-inflammatory Drug. The mechanism of action of mefenamic acid is as a Cyclooxygenase Inhibitor. The chemical classification of mefenamic acid is Nonsteroidal Anti-inflammatory Compounds.(In Vitro):Mefenamic acid is a non-steroidal anti-inflammatory agent, acting as a competitive inhibitor of hCOX-1, with IC50s of 40 nM and 3 μM for hCOX-1 and hCOX-2, respectively. Mefenamic acid (0-100 μM) has cytotoxic effects on KB, Saos-2, and 1321N cells, however, U-87MG cells are resistant to Mefenamic acid.
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In VitroMefenamic acid is a non-steroidal anti-inflammatory agent, acting as a competitive inhibitor of hCOX-1, with IC50s of 40 nM and 3 μM for hCOX-1 and hCOX-2, respectively. Mefenamic acid (0-100 μM) has cytotoxic effects on KB, Saos-2, and 1321N cells, however, U-87MG cells are resistant to Mefenamic acid.
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In Vivo——
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SynonymsC.I. 473 | NSC 94437
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PathwayChromatin/Epigenetic
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TargetCOX
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RecptorCOX-1| COX-2
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Research AreaInflammation/Immunology
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Indication——
Chemical Information
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CAS Number61-68-7
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Formula Weight241.29
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Molecular FormulaC15H15NO2
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Purity>98% (HPLC)
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SolubilityDMSO: 48 mg/mL (198.93 mM)
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SMILESc1(c(cccc1)C(=O)O)Nc1c(c(ccc1)C)C
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Chemical Name2-(2,3-dimethylanilino)benzoic acid
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Bhat AS, et al. Eur J Pharmacol. 2007 Feb 5; 556(1-3):190-9.
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