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AB120354

Flufenamic acid, COX inhibitor

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(2 Publications)

MW 281.23 Da, Purity >98%. Non-steroidal anti-inflammatory. Potently inhibits human transthyretin amyloid fibril formation. Alters ion fluxes through the plasma membrane. Potent non-specific blocker of cation and anion channels, commonly used to block currents through TRP channels and receptor-operated channels.
2 Images
Functional Studies - Flufenamic acid, COX inhibitor (AB120354)
  • FuncS

Unknown

Functional Studies - Flufenamic acid, COX inhibitor (AB120354)

ab51110 staining AMPKα 1 + AMPKα 2 (phosphoT172) in HeLa cells treated with flufenamic acid (ab120354), by ICC/IF. Increase in AMPKα 1 + AMPKα 2 (phosphoT172) nuclear expression correlates with increased concentration of flufenamic acid, as described in literature.
The cells were incubated at 37°C for 30 minutes in media containing different concentrations of ab120354 (flufenamic acid) in DMSO, fixed with 4% formaldehyde for 10 minutes at room temperature and blocked with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% tween for 2h at room temperature. Staining of the treated cells with ab51110 (5 µg/ml) was performed overnight at 4°C in PBS containing 1% BSA and 0.1% tween. A DyLight® 488 goat anti-rabbit polyclonal antibody (ab96899) at 1/250 dilution was used as the secondary antibody.

Chemical Structure - Flufenamic acid, COX inhibitor (AB120354)
  • Chemical Structure

Lab

Chemical Structure - Flufenamic acid, COX inhibitor (AB120354)

2D chemical structure image of ab120354, Flufenamic acid, COX inhibitor

Key facts

CAS number

530-78-9

Purity

>98%

Form

Solid

form

Molecular weight

281.23 Da

Molecular formula

C<sub>1</sub><sub>4</sub>H<sub>1</sub><sub>0</sub>F<sub>3</sub>NO<sub>2</sub>

PubChem

3371

Nature

Synthetic

Solubility

Soluble in DMSO to 100 mM

Soluble in ethanol to 100 mM

Biochemical name

Flufenamic acid

Biological description

Non-steroidal anti-inflammatory. Potently inhibits human transthyretin amyloid fibril formation. Alters ion fluxes through the plasma membrane. Potent non-specific blocker of cation and anion channels, commonly used to block currents through TRP channels and receptor-operated channels.

Canonical smiles

C1=CC=C(C(=C1)C(=O)O)NC2=CC=CC(=C2)C(F)(F)F

InChi

InChI=1S/C14H10F3NO2/c15-14(16,17)9-4-3-5-10(8-9)18-12-7-2-1-6-11(12)13(19)20/h1-8,18H,(H,19,20)

InChiKey

LPEPZBJOKDYZAD-UHFFFAOYSA-N

IUPAC Name

2-[3-(trifluoromethyl)anilino]benzoic acid

Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
Ambient
Appropriate long-term storage conditions
Ambient
Storage information
The product can be stored for up to 12 months

Product protocols

Publications (2)

Recent publications for all applications. Explore the full list and refine your search

Investigative ophthalmology & visual science 62:28 PubMed34427623

2021

iPSC-Derived Trabecular Meshwork Cells Stimulate Endogenous TM Cell Division Through Gap Junction in a Mouse Model of Glaucoma.

Applications

Unspecified application

Species

Unspecified reactive species

Shangru Sui,Hongxia Yu,Xiangji Wang,Wenyan Wang,Xuejiao Yang,Xiaojing Pan,Qingjun Zhou,Chen Xin,Rong Du,Shen Wu,Jingxue Zhang,Qilong Cao,Ningli Wang,Markus H Kuehn,Wei Zhu

Journal of diabetes research 2016:7262680 PubMed26788521

2016

Connexin-Based Therapeutics and Tissue Engineering Approaches to the Amelioration of Chronic Pancreatitis and Type I Diabetes: Construction and Characterization of a Novel Prevascularized Bioartificial Pancreas.

Applications

Unspecified application

Species

Unspecified reactive species

J Matthew Rhett,Hongjun Wang,Heather Bainbridge,Lili Song,Michael J Yost
View all publications

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