Uridine 5′-diphosphoglucose-13C6 (disodium)

CAT:
804-HY-N7032S1
Size:
1 mg

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Uridine 5′-diphosphoglucose-13C6 (disodium) - image 1

Uridine 5′-diphosphoglucose-13C6 (disodium)

  • UNSPSC Description:

    Uridine 5′-diphosphoglucose-13C6 (disodium) is the 13C labeled Uridine 5′-diphosphoglucose disodium salt[1]. Uridine 5′-diphosphoglucose disodium salt (UDP-D-Glucose disodium salt) is the precursor of glucose-containing oligosaccharides, polysaccharides, glycoproteins, and glycolipids in animal tissues and in some microorganisms. Uridine-5′-diphosphoglucose is an agonist of the P2Y14 receptor, a neuroimmune system GPCR[2].
  • Target Antigen:

    Endogenous Metabolite; P2Y Receptor
  • Type:

    Isotope-Labeled Compounds
  • Related Pathways:

    GPCR/G Protein;Metabolic Enzyme/Protease
  • Applications:

    Neuroscience-Neuromodulation
  • Field of Research:

    Neurological Disease
  • Assay Protocol:

    https://www.medchemexpress.com/uridine-5-diphosphoglucose-13c6-disodium.html
  • Purity:

    98.35
  • Solubility:

    10 mM in DMSO
  • Smiles:

    O[C@H]1[C@H](N2C(NC(C=C2)=O)=O)O[C@@H]([C@H]1O)COP(OP(O[13C@H]3O[13C@@H]([13C@H]([13C@@H]([13C@H]3O)O)O)[13CH2]O)(O[Na])=O)(O[Na])=O
  • Molecular Weight:

    616.22
  • References & Citations:

    [1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216.|[2]DietrichKeppler, et al. Uridine-5′-diphosphoglucose. Methods of Enzymatic Analysis (Second English Edition). 1974;4:2225-2228.|[3]Das A, et al. Human P2Y(14) receptor agonists: truncation of the hexose moiety of uridine-5'-diphosphoglucose and its replacement with alkyl and aryl groups. J Med Chem. 2010 Jan 1453(1):471-80.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

    4°C (Powder, sealed storage, away from moisture)
  • Clinical Information:

    No Development Reported
  • CAS Number:

    2483735-04-0