For research use only. Not for therapeutic Use.
<span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">5-Hydroxy Vioxx (CAS 185147-17-5)<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;"> is a metabolite of Vioxx. The biotransformation of Rofecoxib (Vioxx) is highly dependent on the subcellular fraction and the redox system used.</span></span></span></span>
CAS Number | 185147-17-5 |
Synonyms | 5-Hydroxy-4-[4-(methylsulfonyl)phenyl]-3-phenyl-2(5H)-furanone; 5-Hydroxyrofecoxib; |
Molecular Formula | C17H14O5S |
Purity | ≥95% |
Storage | Store at RT |
IUPAC Name | 2-hydroxy-3-(4-methylsulfonylphenyl)-4-phenyl-2H-furan-5-one |
InChI | InChI=1S/C17H14O5S/c1-23(20,21)13-9-7-12(8-10-13)15-14(16(18)22-17(15)19)11-5-3-2-4-6-11/h2-10,17,19H,1H3 |
InChIKey | NCBVUSNBLYMFPP-UHFFFAOYSA-N |
SMILES | CS(=O)(=O)C1=CC=C(C=C1)C2=C(C(=O)OC2O)C3=CC=CC=C3 |
Reference | <span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">1.<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Funaki, T., et al. "In vivo oxidative cleavage of a pyridinecarboxylic acid ester metabolite of nifedipine." </span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Biochemical pharmacology</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;"> 38.23 (1989): 4213-4216.<br /> |