N0630

Niflumic acid

synthetic (organic), ≥98% (HPLC), COX-2 inhibitor, GABAARs antagonist and CaCC inhibitor, powder

• Synonim(y): 2-(α,α,α-Trifluoro-m-toluidino)nicotinic acid, 2-[3-(Trifluoromethyl)anilino]nicotinic acid
• Wzór empiryczny (zapis Hilla): C₁₃H₉F₃N₂O₂
• Numer CAS: 4394-00-7
• Masa cząsteczkowa: 282.22
• NACRES: NA.77
• PubChem Substance ID: 24278582
• UNSPSC Code: 12352106
• EC Number: 224-516-2
• MDL number: MFCD00010569
• Assay: ≥98% (HPLC)
• Form: powder

Właściwości

• Nazwa produktu: Niflumic acid,
• biological source: synthetic (organic)
• Quality Segment: 100
• assay: ≥98% (HPLC)
• form: powder
• mp: 203-204 °C
• solubility: acetone: 50 mg/mL, clear to slightly hazy, yellow
• SMILES string: O=C(O)C1=CC=CN=C1NC2=CC(C(F)(F)F)=CC=C2
• InChI: 1S/C13H9F3N2O2/c14-13(15,16)8-3-1-4-9(7-8)18-11-10(12(19)20)5-2-6-17-11/h1-7H,(H,17,18)(H,19,20)
• InChI key: JZFPYUNJRRFVQU-UHFFFAOYSA-N
• Gene Information: human ... PTGS1(5742)

Opis

Application

Niflumic acid has been used:

• as a chloride channel blocker in mouse olfactory epithelium for odor-induced electroolfactograms (EOGs) measurements[1], to test its analgesic effect on rat dorsal root ganglion neurons post γ-aminobutyric acid induction[2]
• as a calcium-activated chloride channel (CaCC) inhibitor in C2C12 myoblasts and also to test its effect on volume-regulated anion channel (VRAC)[3]
• as an inhibitor of voltage-dependent potassium channel in human embryonic kidney (HEK 293) phoenix cells[4]

Biochem/physiol Actions

Niflumic acid (NFA), a γ-aminobutyric acid type A receptor (GABAARs) antagonist [2] is a non-steroidal anti-inflammatory drug (NSAID) and it belongs to the fenamate class.[4] It is also a blocker of chloride ion channel[2] and a calcium-activated chloride channel (CaCC) inhibitor.[3] NFA possesses anti-inflammatory property and is useful in treating rheumatic disorders.[4] It is also an inhibitor of N-methyl-D-aspartate receptor[4] and glycine receptor.[5] NFA also inhibits enzymes associated with the prostaglandins synthesis.[5]

Selective cyclooxygenase-2 (COX-2) inhibitor.

Features and Benefits

This compound is featured on the Chloride Channels and Potassium Channels pages of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

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Informacja o środkach bezpieczeństwa

• pictograms: GHS06
• signalword: Danger
• hcodes: H301,H413
• pcodes: P264 - P270 - P273 - P301 + P310 - P405 - P501
• Hazard Classifications: Acute Tox. 3 Oral - Aquatic Chronic 4
• Klasa składowania: 6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
• wgk: WGK 3
• ppe: dust mask type N95 (US), Eyeshields, Faceshields, Gloves