5-Hydroxy Vioxx

For research use only. Not for therapeutic Use.

  • CAT Number: R013109
  • CAS Number: 185147-17-5
  • Molecular Formula: C17H14O5S
  • Molecular Weight: 330.354
  • Purity: ≥95%
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<span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">5-Hydroxy Vioxx (CAS&nbsp;185147-17-5)<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;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. &quot;In vivo oxidative cleavage of a pyridinecarboxylic acid ester metabolite of nifedipine.&quot;&nbsp;</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;">&nbsp;38.23 (1989): 4213-4216.<br />
2.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">John, B. A., et al. &quot;Metabolism of the anti-psoriatic agent 5-methoxypsoralen in humans: comparison with rat and dog.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Xenobiotica</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;22.11 (1992): 1339-1351.<br />
3.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Jouzeau, Jean-Yves, et al. &quot;Cyclo-oxygenase isoenzymes.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Drugs</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;53.4 (1997): 563-582.<br />
4.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Baillie, Thomas A., et al. &quot;Mechanistic studies on the reversible metabolism of rofecoxib to 5-hydroxyrofecoxib in the rat: evidence for transient ring opening of a substituted 2-furanone derivative using stable isotope-labeling techniques.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Drug metabolism and disposition</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;29.12 (2001): 1614-1628.</span></span></span></span>

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