Bufexamac
CAS No. 2438-72-4
Bufexamac( Bufexamac | CP-1044-J-3 | CP 1044 J 3 | CP1044J3 | Droxaryl | Parfenac )
Catalog No. M13704 CAS No. 2438-72-4
Bufexamac is a COX inhibitor for IFN-α release.
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 |
|
| 200MG | 35 | In Stock |
|
| 500MG | 48 | In Stock |
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| 1G | 70 | In Stock |
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Biological Information
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Product NameBufexamac
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NoteResearch use only, not for human use.
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Brief DescriptionBufexamac is a COX inhibitor for IFN-α release.
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DescriptionBufexamac is a COX inhibitor for IFN-α release.
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In VitroCell Viability Assay Cell Line:BE(2)-C cells Concentration:30 μM Incubation Time:6 days Result:Enhanced cell death of tumor cells.Cell Migration Assay Cell Line:mouse neutrophils Concentration:50-100 μM Incubation Time:30 min Result:Reduced fMLP (5μM) induced neutrophil migration.Western Blot Analysis Cell Line:Hela cells (ATCC: CCL-2)Concentration:1 mM Incubation Time:4-16 hResult:Induced HIF1-α protein and increased HIF1-α levels.ImmunofluorescenceCell Line:Hela cells (ATCC: CCL-2)Concentration:50-250 μM Incubation Time:4 h Result:Stabilized HIF1-α and accumulated in the nucleus.
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In VivoAnimal Model:Six-to-eight weeks old female C57BL/6 miceDosage:50-100 mg/kg Administration:Oral gavage (p.o.), seven days Result:Ameliorated the infiltration of lung inflammatory cells and injury to the lung in a dose-dependent manner.Relieved LPS-induced lung injury.Reduced LTB4 level and MPO activity.Reduced cytokine mRNA expressions in lung tissue and cytokine levels in BALF in LPS-induced ALI in mice.Animal Model:horses aged 2 to 7 years old and weighing 302 to 522 kg Dosage:20-100 mg Administration:Intraarticular (IA) injection, weekly, 6 times Result:Didn't effect on general health, hematological or serum biochemical variables, or organs.
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SynonymsBufexamac | CP-1044-J-3 | CP 1044 J 3 | CP1044J3 | Droxaryl | Parfenac
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PathwayChromatin/Epigenetic
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TargetCOX
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RecptorIFN-α
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Research AreaInflammation/Immunology
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Indication——
Chemical Information
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CAS Number2438-72-4
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Formula Weight223.27
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Molecular FormulaC12H17NO3
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Purity>98% (HPLC)
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SolubilityEthanol: 3 mg/mL (13.43 mM); DMSO: 45 mg/mL (201.54 mM)
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SMILESO=C(NO)CC1=CC=C(OCCCC)C=C1
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Chemical Name2-(4-butoxyphenyl)-N-hydroxyacetamide
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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Indomethacin sodium ...
Indomethacin sodium hydrate (Indometacin sodium hydrate) is an orally active, competitive and reversible COX1/2 inhibitor with potential anti-inflammatory activity in induced migraines.
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Thonzylamine
Thonzylamine is an antihistamine and anticholinergic drug. It is available as combination products with Clofedanol or Phenylephrine for temporary relief of symptoms of common cold, hay fever (allergic rhinitis) or other upper respiratory allergies.
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4',7-Dihydroxyflavon...
4',7-Dihydroxyflavone can induce transcription of nodulation (nod) genes in Rhizobium meliloti. It has inhibitory activities against COX-2.Root exudate from 3-day-old alfalfa seedlings was purified and then assayed for biological activity with a nodABC-lacZ fusion in R. meliloti.
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