CHEBI:73041 - tilmacoxib

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name tilmacoxib ChEBI ID CHEBI:73041 Definition A member of the class of 1,3-oxazoles that is that is 1,3-oxazole which is substituted at positions 2, 4 and 5 by methyl, cyclohexyl, and 3-fluoro-4-sulfamoylphenyl groups, respectively. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Wikipedia License Read full article at Wikipedia Formula C16H19FN2O3S Net Charge 0 Average Mass 338.39700 Monoisotopic Mass 338.11004 InChI InChI=1S/C16H19FN2O3S/c1-10-19-15(11-5-3-2-4-6-11)16(22-10)12-7-8-14(13(17)9-12)23(18,20)21/h7-9,11H,2-6H2,1H3,(H2,18,20,21) InChIKey MIMJSJSRRDZIPW-UHFFFAOYSA-N SMILES Cc1nc(C2CCCCC2)c(o1)-c1ccc(c(F)c1)S(N)(=O)=O Roles Classification Biological Role(s): cyclooxygenase 2 inhibitor A cyclooxygenase inhibitor that interferes with the action of cyclooxygenase 2. View more via ChEBI Ontology ChEBI Ontology Outgoing tilmacoxib (CHEBI:73041) has role cyclooxygenase 2 inhibitor (CHEBI:50629) tilmacoxib (CHEBI:73041) is a 1,3-oxazoles (CHEBI:46812) tilmacoxib (CHEBI:73041) is a organofluorine compound (CHEBI:37143) tilmacoxib (CHEBI:73041) is a sulfonamide (CHEBI:35358) IUPAC Name 4-(4-cyclohexyl-2-methyl-1,3-oxazol-5-yl)-2-fluorobenzenesulfonamide INNs Sources tilmacoxib WHO MedNet tilmacoxib WHO MedNet tilmacoxib WHO MedNet tilmacoxibum WHO MedNet Synonyms Sources 4-(4-cyclohexyl-2-methyloxazol-5-yl)-2-fluorobenzenesulfonamide ChemIDplus 5-ethoxymethyl-7-fluoro-3-oxo-1,2,3,5-tetrahydrobenzo(4,5)imidazo(1,2a)pyridine-4-N-(2-fluorophenyl)carboxamide ChemIDplus JTE-522 ChemIDplus JTP-19605 ChemIDplus RWJ-57504 ChemIDplus Manual Xrefs Databases D01974 KEGG DRUG Tilmacoxib Wikipedia View more database links Registry Numbers Types Sources 180200-68-4 CAS Registry Number KEGG DRUG 180200-68-4 CAS Registry Number ChemIDplus 9005354 Reaxys Registry Number Reaxys Citations Types Sources 10807499 PubMed citation Europe PMC 11092987 PubMed citation Europe PMC 12445023 PubMed citation Europe PMC 12891558 PubMed citation Europe PMC 16622748 PubMed citation Europe PMC 17914586 PubMed citation Europe PMC 20389170 PubMed citation Europe PMC 20434301 PubMed citation Europe PMC 9427067 PubMed citation Europe PMC 9869271 PubMed citation Europe PMC Last Modified 27 March 2013