CAS RN 530-78-9
CAS RN 530-78-9
Thermo Scientific Chemicals Ácido flufenámico, 97 %
CAS: 530-78-9 Fórmula molecular: C14H10F3NO2 Peso molecular (g/mol): 281.22 Número MDL: MFCD00002422 Clave InChI: LPEPZBJOKDYZAD-UHFFFAOYSA-N Sinónimo: flufenamic acid,fluphenamic acid,nichisedan,achless,arlef,flufacid,fullsafe,lanceat,paraflu,plostene PubChem CID: 3371 ChEBI: CHEBI:42638 Nombre IUPAC: ácido 2-[3-(trifluorometil)anilino]benzoico SMILES: C1=CC=C(C(=C1)C(=O)O)NC2=CC=CC(=C2)C(F)(F)F
Ácido flufenámico, Mikromol™
Descubrir Mikromol - su fuente confiable de estándares de referencia farmacéuticos de alta calidad. Apoyando un análisis preciso y conforme con las normas ISO Materiales acreditados 17034 diseñados para brindar confianza en cada resultado.
Ácido flufenámico, LoGiCal
Materiales de referencia certificados de LoGiCal en forma de soluciones nativas, netas y soluciones marcadas con isótopos estables, con documentación y soporte de expertos. Desde laboratorios forenses hasta laboratorios clínicos, elija LoGiCal para obtener confianza, cumplimiento y excelencia analítica.
Flufenamic Acid, TRC
CAS: 530-78-9 Fórmula molecular: C14 H10 F3 N O2 Peso molecular (g/mol): 281.23 Sinónimo: Flufenamic Acid,Etofenamate Imp. A (EP),2-[3-(Trifluoromethyl)anilino]benzoic acid,2-[[3-(Trifluoromethyl)phenyl]amino]benzoic acid,3'-Trifluoromethyl-N-phenylanthranilic acid,3'-Trifluoromethyldiphenylamine-2-carboxylic acid,ANT-1,Achless,Ansatin,Arlef,CI 440,CN 27544,Flufenamic acid,Fluphenamic acid,Fullsafe,INF 1837,Meralen,Movilizin,N-(α,α,α-Trifluoro-m-tolyl)anthranilic acid,N-(m-Trifluoromethylphenyl)-2-aminobenzoic acid,N-[3-(Trifluoromethyl)phenyl]anthranilic acid,NSC 219007,NSC 82699,Paraflu,Parlef,Parlif,Pinox,Plostene,Ristogen,Sastridex,Surika,Tecramine Nombre IUPAC: 2-[3-(trifluoromethyl)anilino]benzoic acid SMILES: OC(=O)c1ccccc1Nc2cccc(c2)C(F)(F)F
Flufenamic acid, MedChemExpress
MedChemExpress Flufenamic acid is a non-steroidal anti-inflammatory agent, inhibits cyclooxygenase (COX), activates AMPK, and also modulates ion channels, blocking chloride channels and L-type Ca2+ channels, modulating non-selective cation channels (NSC), activating K+ channels. Flufenamic acid binds to the central pocket of TEAD2 YBD and inhibits both TEAD function and TEAD-YAP-dependent processes, such as cell migration and proliferation.
