CAS RN 530-78-9
Thermo Scientific Chemicals Flufenaminsyre, 97%
CAS: 530-78-9 Molekylær formel: C14H10F3NO2 Molekylvægt (g/mol): 281.22 MDL nummer: MFCD00002422 InChI nøgle: LPEPZBJOKDYZAD-UHFFFAOYSA-N Synonym: flufenamic acid,fluphenamic acid,nichisedan,achless,arlef,flufacid,fullsafe,lanceat,paraflu,plostene PubChem CID: 3371 ChEBI: CHEBI:42638 IUPAC navn: 2-[3-(trifluormethyl)anilino]benzoesyre SMIL: C1=CC=C(C(=C1)C(=O)O)NC2=CC=CC(=C2)C(F)(F)F
Flufenaminsyre, Mikromol™
Discover Mikromol – din pålidelige kilde til farmaceutiske referencestandarder af høj kvalitet. Understøttelse af nøjagtig, overensstemmende analyser med ISO 17034-akkrediterede materialer, der er designet til at sikre tillid til hvert resultat.
Flufenaminsyre, LoGiCal
LoGiCals certificerede referencematerialer som smarte, native løsninger og stabile isotop-mærkede løsninger, med ekspertdokumentation og support. Fra retsmedicinske til kliniske laboratorier – vælg LoGiCal for selvtillid, overholdelse og analytisk ekspertise.
Flufenaminsyre, TRC
CAS: 530-78-9 Molekylær formel: C14 H10 F3 N O2 Molekylvægt (g/mol): 281.23 Synonym: 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 IUPAC navn: 2-[3-(trifluoromethyl)anilino]benzoesyre SMIL: 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.