Oxonic Acid (potassium salt)
CAS No. 2207-75-2
Oxonic Acid (potassium salt)( Potassium azaorotate | Potassium otastat | Potassium oxonate )
Catalog No. M20562 CAS No. 2207-75-2
Oxonic Acid (potassium salt) is a uricase inhibitor that prevents metabolism and excretion of uric acid and induces embryotoxicity and nephrotoxicity in rats.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product NameOxonic Acid (potassium salt)
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NoteResearch use only, not for human use.
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Brief DescriptionOxonic Acid (potassium salt) is a uricase inhibitor that prevents metabolism and excretion of uric acid and induces embryotoxicity and nephrotoxicity in rats.
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DescriptionOxonic Acid (potassium salt) is a uricase inhibitor that prevents metabolism and excretion of uric acid and induces embryotoxicity and nephrotoxicity in rats.
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In Vitro——
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In Vivo——
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SynonymsPotassium azaorotate | Potassium otastat | Potassium oxonate
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PathwayOthers
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TargetOther Targets
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Recptoruricase
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Research Area——
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Indication——
Chemical Information
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CAS Number2207-75-2
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Formula Weight195.17
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Molecular FormulaC4H2KN3O4
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Purity>98% (HPLC)
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SolubilityH2O:9.09 mg/mL (46.57 mM; Need ultrasonic)
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SMILES[K+].[O-]C(=O)c1nc(=O)[nH]c(=O)[nH]1
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Chemical NamePotassium 1456-tetrahydro-46-dioxo-135-triazine-2-carboxylate
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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CALP1
Cell-permeable calmodulin (CaM) agonist that binds to the EF-hand/Ca2+-binding site; produces CaM-dependent activation of phosphodiesterase. Also binds to cytoplasmic sites on other Ca2+ channels, including NMDA and HIV-1 gp120-activated channels, inhibiting Ca2+-mediated cytotoxicity and apoptosis (IC50 = 52 μM). Shown to protect pancreatic acinar cells from gossypol induced necrosis. Inhibits VLA-5-mediated adhesion of mast cells to fibronectin in vitro and attenuates inflammatory cell influx in guinea pig lung in vivo.
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Propargyl-PEG13-brom...
Propargyl-PEG13-bromide is a PEG derivative containing a propargyl group.
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δ-Valerolactone
δ-Valerolactone is a compound commonly used to synthesize copolyesters by means of lipase-catalyzed ring-opening polymerization.
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