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Oxonic Acid-13C2,15N3 (potassium salt hydrate)

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    Oxonic Acid-<sup>13</sup>C<sub>2</sub>,<sup>15</sup>N<sub>3</sub> (potassium salt hydrate)
  • Oxonic Acid-<sup>13</sup>C<sub>2</sub>,<sup>15</sup>N<sub>3</sub> (potassium salt hydrate)
Cat No: 33282
Biochemicals - Isotopically Labeled Standards
Cayman

Oxonic acid-13C2,15N3 is intended for use as an internal standard for the quantification of oxonic acid (potassium salt) (Item No. 22586) by GC- or LC-MS. Oxonic acid is a uricase inhibitor (IC50 = 0.8 µM) that prevents metabolism and excretion of uri...

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: 1 mg

This product can only be bought through Cayman Chemical. Please contact us.

Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 4,6-dioxo-1,4,5,6-tetrahydro-1,3,5-triazine-2-carboxylate-4,6-13C2-1,3,5-15N3
Correlated keywords:
  • deuterated deuterium GCMS LCMS OPRTmediated 5fluorouracil 5FU
Product Overview:
Oxonic acid-13C2,15N3 is intended for use as an internal standard for the quantification of oxonic acid (potassium salt) (Item No. 22586) by GC- or LC-MS. Oxonic acid is a uricase inhibitor (IC50 = 0.8 µM) that prevents metabolism and excretion of uric acid.{58362,40118} It also inhibits orotate phosphoribosyltransferase (ORPT), reducing OPRT-mediated phosphorylation of 5-fluorouracil (5-FU; Item No. 14416) in Yoshida sarcoma cell extracts with an IC50 value of 3.7 µM.{58363} Oxonic acid (10-50 mg/kg) decreases the severity of gastrointestinal tract injury and the incidence of diarrhea induced by the 5-FU prodrug tegafur (Item No. 26076) and uracil (Item No. 26088) without loss of antitumor activity in a rat Yoshida sarcoma model. It has also been used to induce hyperuricemia in rodents.{58364} Formulations containing oxonic acid have been used in the treatment of head, neck, lung, pancreatic, gastric, and breast carcinomas.
Size 1 mg
Shipping dry ice
Molecular Formula C2[13C]2H2[15N]3O4 • K [XH2O]
SMILES O=[13C]([15N]=C(C([O-])=O)[15NH]1)[15NH][13C]1=O.[K+].O
Molecular Weight 200,1
Formulation A solid
Purity ≥95%
Custom Code 3822.19
UNSPSC code 12352100

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Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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ISO Guide 34:2009

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