Uridine

CAT:
804-HY-B1449-01
Size:
100 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Uridine - image 1

Uridine

  • Description :

    Uridine (β-Uridine) is a nucleoside compound composed of uracil and a ribose ring, which are connected by a β-N1-glycosidic bond[1].
  • CAS Number :

    [58-96-8]
  • Product Name Alternative :

    β-Uridine
  • UNSPSC :

    12352005
  • Hazard Statement :

    H302, H315, H319, H335
  • Target :

    Endogenous Metabolite; NF-κB; Nucleoside Antimetabolite/Analog
  • Type :

    Natural Products
  • Related Pathways :

    Cell Cycle/DNA Damage; Metabolic Enzyme/Protease; NF-κB
  • Applications :

    Metabolism-protein/nucleotide metabolism
  • Field of Research :

    Cancer
  • Assay Protocol :

    https://www.medchemexpress.com/Uridin.html
  • Purity :

    99.98
  • Solubility :

    DMSO : 50 mg/mL (ultrasonic) |H2O : ≥ 100 mg/mL
  • Smiles :

    O[C@H]1[C@@H](O)[C@H](N2C(NC(C=C2)=O)=O)O[C@@H]1CO
  • Molecular Formula :

    C9H12N2O6
  • Molecular Weight :

    244.20
  • Precautions :

    H302, H315, H319, H335
  • References & Citations :

    [1]Sokoloski JA, et al., Effects of uridine on the growth and differentiation of HL-60 leukemia cells. Leuk Res. 1991;15 (11) :1051-8. |[2]Zheng WV, et al., Uridine alleviates carbon tetrachloride-induced liver fibrosis by regulating the activity of liver-related cells. J Cell Mol Med. 2022 Feb;26 (3) :840-854. |[3]Krylova IB, et al., Uridine treatment prevents myocardial injury in rat models of acute ischemia and ischemia/reperfusion by activating the mitochondrial ATP-dependent potassium channel. Sci Rep. 2021 Aug 20;11 (1) :16999.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

    Store at room temperature 3 years
  • Scientific Category :

    Natural Products
  • Clinical Information :

    Launched
  • Isoform :

    Human Endogenous Metabolite

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