GLPBio

Oxonic acid potassium salt

Catalog No.: GC17025Purity:>98.00%Synonyms: Allantoxanic Acid, Potassium oxonate
Oxonic acid potassium salt selectively and competitively inhibits the activity of uricase, effectively elevating uric acid levels in vivo. Oxonic acid potassium salt inhibits the phosphorylation of 5-fluorouracil (5-FU) to 5-fluorouridine-5'-monophosphate.

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Oxonic acid potassium salt
Cas No.: 2207-75-2
10mM (in 1mL Water)In Stock
$45.00
1
500mgIn Stock
$36.00
1
5gIn Stock
$45.00
1

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Description

Oxonic acid potassium salt selectively and competitively inhibits the activity of uricase, effectively elevating uric acid levels in vivo. Oxonic acid potassium salt inhibits the phosphorylation of 5-fluorouracil (5-FU) to 5-fluorouridine-5'-monophosphate[1-2]. Oxonic acid potassium salt can be used to establish animal models of hyperuricemia and serves as an auxiliary tool in cancer research[3-4].

In vivo, treatment of Kunming mice with Oxonic acid potassium salt (350mg/kg/day) combined with Hypoxanthine (450mg/kg/day) via intraperitoneal injection and oral gavage for 8 consecutive weeks induced a chronic hyperuricemia model, Oxonic acid potassium salt significantly led to left ventricular anterior wall thickening, myocardial structural disorganization, increased cardiac mass, and was accompanied by complications such as renal enlargement and renal tubule dilation[5]. Treatment of Kunming mice with Oxonic acid potassium salt (350mg/kg/day) combined with Hypoxanthine (450mg/kg/day) via intraperitoneal injection and oral gavage for 1 consecutive week induced a hyperuricemia model, Oxonic acid potassium salt significantly decrease in polyamine levels in cardiomyocytes and upregulation of the protein expression of the key polyamine synthesis enzyme ODC1 and the metabolic enzyme SAT1, leading to cardiomyocyte injury[6].

References:
[1] Zhang N, Zhang B, Chen X, et al. Effects and mechanisms of Polygonati Rhizoma polysaccharide on potassium oxonate and hypoxanthine-induced hyperuricemia in mice. Int J Biol Macromol. 2024 Sep 13;280(Pt 1):135550.
[2] Yamashita T, Ueda Y, Fuji N, et al. Potassium oxonate, an enzyme inhibitor compounded in S-1, reduces the suppression of antitumor immunity induced by 5-fluorouracil. Cancer Chemother Pharmacol. 2006 Aug;58(2):183-8.
[3] Tian J, Wang B, Xie B, et al. Pyroptosis inhibition alleviates potassium oxonate- and monosodium urate-induced gouty arthritis in mice. Mod Rheumatol. 2022 Jan 5;32(1):221-230.
[4] Yoshisue K, Hironaga K, Yamaguchi S, et al. Reduction of 5-fluorouracil (5-FU) gastrointestinal (GI) toxicity resulting from the protection of thymidylate synthase (TS) in GI tissue by repeated simultaneous administration of potassium oxonate (Oxo) in rats. Cancer Chemother Pharmacol. 2000;46(1):51-6.
[5] Lin C, Zheng Q, Li Y, et al. Assessment of the influence on left ventricle by potassium oxonate and hypoxanthine-induced chronic hyperuricemia. Exp Biol Med (Maywood). 2023 Jan;248(2):165-174.
[6] Lin C, Zheng Q, Yu H, et al. Uric acid-induced cardiomyocytic polyamines' insufficience: a potential mechanism mediates cardiomyocytic injury. Front Endocrinol (Lausanne). 2025 Apr 7;16:1504614.

Protocol

Animal experiment [1]:

Animal models

Kunming (KM) mice

Preparation Method

Mice were intraperitoneally administered Oxonic acid potassium salt (350mg/kg/day) combined with oral hypoxanthine (450mg/kg/day) for 8 weeks. Cardiac function and histopathology were assessed post-treatment.

Dosage form

350mg/kg/day; i.p; Daily administration for 8 weeks.

Applications

Oxonic acid potassium salt and hypoxanthine co-administration induced chronic hyperuricemia, leading to left ventricular remodeling characterized by anterior wall thickening, myocardial disorganization, inflammatory infiltration, and collagen fibrosis.

References:
[1] Lin C, Zheng Q, Li Y, et al. Assessment of the influence on left ventricle by potassium oxonate and hypoxanthine-induced chronic hyperuricemia. Exp Biol Med (Maywood). 2023 Jan;248(2):165-174.

Product Documents

Purity:>98.00%Appearance:A solid

Chemical Properties

CAS No.
2207-75-2
Synonyms
Allantoxanic Acid, Potassium oxonate
Chemical Name
potassium;4,6-dioxo-1H-1,3,5-triazine-2-carboxylate
SMILES
C1(=NC(=O)NC(=O)N1)C(=O)[O-].[K+]
Molecular Formula
C4H2KN3O4
Molecular Weight
195.17
Solubility
≥ 19.5mg/mL in Water with gentle warming
Storage
Store at -20°C
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

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