Diclofenac Epolamine
CAS No. 119623-66-4
Diclofenac Epolamine( DHEP | DIEP | diclofenac hydroxyethylpyrrolidine )
Catalog No. M27544 CAS No. 119623-66-4
Diclofenac Epolamine is a non-steroidal anti-inflammatory agent (NSAID) with analgesic and antipyretic actions.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 36 | Get Quote |
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10MG | 51 | Get Quote |
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25MG | 85 | Get Quote |
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50MG | 124 | Get Quote |
|
100MG | 178 | Get Quote |
|
200MG | 267 | Get Quote |
|
500MG | Get Quote | Get Quote |
|
1G | Get Quote | Get Quote |
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Biological Information
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Product NameDiclofenac Epolamine
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NoteResearch use only, not for human use.
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Brief DescriptionDiclofenac Epolamine is a non-steroidal anti-inflammatory agent (NSAID) with analgesic and antipyretic actions.
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DescriptionDiclofenac Epolamine is a non-steroidal anti-inflammatory agent (NSAID) with analgesic and antipyretic actions.
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In VitroFlector Patch (Diclofenac epolamine) (1.3% w/w, 24 hours) increases diclofenac partitioning into the skin.Flector Patch (Diclofenac epolamine) (1.3% w/w) loaded by Microemulsion (ME) enhances the transport of drug through skin and sustains to 12 h after removal of ME.
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In VivoFlector Patch (Diclofenac epolamine) (1.3% w/w, exteral application) displays effective in treating inflammatory conditions. Animal Model:Rat paw edema inflammation model (induced with carrageenan)Dosage:1.3% w/w Administration:Exteral application Result:Inhibited edema and showed anti-inflammatory efficacy at 6 hours after application.
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SynonymsDHEP | DIEP | diclofenac hydroxyethylpyrrolidine
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PathwayOthers
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TargetOther Targets
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RecptorVoltage-gated sodium channel
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Research Area——
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Indication——
Chemical Information
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CAS Number119623-66-4
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Formula Weight411.32
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Molecular FormulaC20H24Cl2N2O3
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Purity>98% (HPLC)
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Solubility——
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SMILESOCCN1CCCC1.OC(=O)Cc1ccccc1Nc1c(Cl)cccc1Cl
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Chemical Name——
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.Ilyin VI, et al. V102862 (Co 102862): a potent, broad-spectrum state-dependent blocker of mammalian voltage-gated sodium channels. Br J Pharmacol. 2005 Mar;144(6):801-12.
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