Uridine diphosphate glucose

  • CAT Number: M070868
  • CAS Number: 133-89-1
  • Molecular Formula: C15H24N2O17P2
  • Molecular Weight: 566.302
  • Purity: ≥95%
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<span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;"><span style="text-align: justify;">Uridine diphosphate glucose(CAS&nbsp;</span>133-89-1)<span style="text-align: justify;">&nbsp;is the precursor of glucose-containing oligosaccharides, polysaccharides, glycoproteins, and glycolipids in animal tissues and in some microorganisms. Uridine diphosphate glucose is an agonist of the P2Y</span><sub style="position: relative; display: inline-block; font-size: 0.9em; line-height: 12px; transform: scale(0.8); top: 0px; color: rgb(51, 21, 21); font-family: Arial, -apple-system, sans-serif; text-align: justify;">14</sub><span style="text-align: justify;">&nbsp;receptor, a neuroimmune system GPCR.</span></span></span></span>

Catalog Number M070868
CAS Number 133-89-1
Molecular Formula

C15H24N2O17P2

Purity 95%
Storage -20°C
Related CAS 28053-08-9(sodium salt)
IUPAC Name [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] hydrogen phosphate
InChI InChI=1S/C15H24N2O17P2/c18-3-5-8(20)10(22)12(24)14(32-5)33-36(28,29)34-35(26,27)30-4-6-9(21)11(23)13(31-6)17-2-1-7(19)16-15(17)25/h1-2,5-6,8-14,18,20-24H,3-4H2,(H,26,27)(H,28,29)(H,16,19,25)/t5-,6-,8-,9-,10+,11-,12-,13-,14-/m1/s1
InChIKey HSCJRCZFDFQWRP-JZMIEXBBSA-N
SMILES C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)OC3C(C(C(C(O3)CO)O)O)O)O)O
Reference

<span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">1.<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">F&uuml;hring, Jana Indra, et al. &quot;A quaternary mechanism enables the complex biological functions of octameric human UDP-glucose pyrophosphorylase, a key enzyme in cell metabolism.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Scientific reports</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;5.1 (2015): 1-11.<br />
2.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Wahlefeld, A. W., and H. U. Bergmeyer. &quot;Methods of enzymatic analysis.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Triglycerides determination after enzymatic hydrolysis. 2nd English ed., Academic Press, Inc, New York</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;(1974): 18-31.<br />
3.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Das, Arijit, et al. &quot;Human P2Y14 receptor agonists: truncation of the hexose moiety of uridine-5&prime;-diphosphoglucose and its replacement with alkyl and aryl groups.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Journal of medicinal chemistry</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;53.1 (2010): 471-480.</span></span></span>

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