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Nifenazone
CAS No. 2139-47-1
Nifenazone( N-Antipyrinylnicotinamide, Niapyrin, Nicazane, Nicodon, Nicodone, Nicofesone )
Catalog No. M13417 CAS No. 2139-47-1
Nifenazone is a drug that has been used as an analgesic for a number of rheumatic conditions.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 28 | In Stock |
|
| 100MG | 27 | In Stock |
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| 200MG | 36 | In Stock |
|
| 500MG | 60 | In Stock |
|
| 1G | 87 | In Stock |
|
Biological Information
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Product NameNifenazone
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NoteResearch use only, not for human use.
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Brief DescriptionNifenazone is a drug that has been used as an analgesic for a number of rheumatic conditions.
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DescriptionNifenazone is a drug that has been used as an analgesic for a number of rheumatic conditions.
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In Vitro——
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In Vivo——
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SynonymsN-Antipyrinylnicotinamide, Niapyrin, Nicazane, Nicodon, Nicodone, Nicofesone
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PathwayChromatin/Epigenetic
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TargetCOX
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RecptorCOX
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Research Area——
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Indication——
Chemical Information
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CAS Number2139-47-1
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Formula Weight308.34
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Molecular FormulaC17H16N4O2
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Purity>98% (HPLC)
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SolubilitySoluble in DMSO
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SMILESCc1c(c(=O)n(n1C)c2ccccc2)NC(=O)c3cccnc3
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Chemical NameNicotinamide, N-(2,3-dimethyl-5-oxo-1-phenyl-3-pyrazolin-4-yl)-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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COX-2-IN-6
COX-2-IN-6 is a potent, selective, and orally available cyclooxygenase-2 (COX-2) inhibitor with an IC50 of 0.84 μM and a Ki of 69 nM.COX-2-IN-6 inhibits COX-2-driven PGE2 synthesis with an IC50 of 0.60 μM.COX-2-IN-6 is used to prevent colorectal cancer.
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Dexketoprofen tromet...
Dexketoprofen trometamol is a modified non-selective COX inhibitor with a rapid onset of action that is available as both oral and parenteral formulations.
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Hamaudol
Hamaudol is a chromone isolated from Saposhnikovia divaricata,has analgesic and anti-inflammary activities, it showed inhibitory activity on COX-1 and COX-2 activities with values of 0.30, 0.57 mM, respectively.The CHCl3 extract of the root of Angelica japonica showed high inhibitory activity against human gastric adenocarcinoma (MK-1) cell growth.
