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(2S,3S,4R,5R,6R)-6-[[[(2S,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxy-3,4,5-trihydroxy-oxane-2-carboxylic

(2S,3S,4R,5R,6R)-6-[[[(2S,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxy-3,4,5-trihydroxy-oxane-2-carboxylic Struktur
2616-64-0
CAS-Nr.
2616-64-0
Englisch Name:
(2S,3S,4R,5R,6R)-6-[[[(2S,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxy-3,4,5-trihydroxy-oxane-2-carboxylic
Synonyma:
UDP-glucuronic acid;UDP-glucuronate;UDP-g acid;UDP-Ghucuronie Acid;UDPg acid,UDP g acid;Glucuronic Acid, UDP;UDP-D-glucuronic acid;UDP-α-D-glucuronicaci;UDP-α-D-galacturonic acid;UDP-alpha-D-glucuronic acid
CBNumber:
CB21236437
Summenformel:
C15H22N2O18P2
Molgewicht:
580.29
MOL-Datei:
2616-64-0.mol

(2S,3S,4R,5R,6R)-6-[[[(2S,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxy-3,4,5-trihydroxy-oxane-2-carboxylic Eigenschaften

Dichte
2.05±0.1 g/cm3(Predicted)
pka
1.10±0.50(Predicted)
InChIKey
HDYANYHVCAPMJV-ARRNFTAONA-N
SMILES
O[C@@H]1[C@@H]([C@@H](COP(O)(=O)OP(O)(=O)O[C@@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](C(=O)O)O2)O)O[C@H]1N1C=CC(=O)NC1=O)O |&1:1,2,3,14,15,16,18,20,27,r|
CAS Datenbank
2616-64-0

Sicherheit

(2S,3S,4R,5R,6R)-6-[[[(2S,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxy-3,4,5-trihydroxy-oxane-2-carboxylic Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

An intermediate in the phase II reaction that results in the formation of glucuro_x0002_nic acid conjugates of xenobiotics which contain substituents such as hydroxyl, amino, or sulfhydryl groups, forming the O-, N-, and S-glucuronides, respectively. UDPGA is formed by two reactions: (i) the formation of UDPG from UTP and glucose 1-phosphate and (ii) the formation of UDPGA from UDPG. The two reactions are catalyzed by UDPG pyrophosphorylase and UDPG dehydrogenase, respectively, whereas glucuronide formation is catalyzed by glucuronosyltransferase. Glucuronide formation from xenobiotics is common in all animal groups except insects.

Definition

ChEBI: A UDP-sugar having alpha-D-glucuronic acid as the sugar component.

(2S,3S,4R,5R,6R)-6-[[[(2S,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxy-3,4,5-trihydroxy-oxane-2-carboxylic Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


(2S,3S,4R,5R,6R)-6-[[[(2S,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxy-3,4,5-trihydroxy-oxane-2-carboxylic Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

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2616-64-0()Verwandte Suche:


  • (2S,3S,4R,5R,6R)-6-[[[(2S,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxy-3,4,5-trihydroxy-oxane-2-carboxylic
  • UDP-D-glucuronic acid
  • Uridine 5'-(trihydrogen diphosphate)mono-α-D-glucopyranuronosyl
  • Uridine diphosphoglucuronic acid
  • Uridine pyrophosphoglucuronic acid
  • UDP-alpha-D-glucuronic acid
  • Uridine diphosphate glucuronic acid
  • Uridine 5′-diphosphoglucuronic acid (UDP-glucuronic acid)
  • UDP-g acid
  • α-D-Glucopyranuronic acid, 1→P'-ester with uridine 5'-(trihydrogen diphosphate)
  • (2S,3S,4R,5R,6R)-6-[[[(2S,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-yl]methoxy-hydroxy-phosphoryl]oxy-hydroxy-phosphoryl]oxy-3,4,5-trihydroxy-oxane-2-carboxylic USP/EP/BP
  • UDP-glucuronic acid
  • UDP-glucuronate
  • UDP-α-D-glucuronicaci
  • P'-ester with uridine5'-(trihydrogen diphosphate)
  • UDPg acid,UDP g acid
  • Glucuronic Acid, UDP
  • (2S,3S,4R,5R,6R)-6-[[[(2S,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolan-2-
  • UDP-Ghucuronie Acid
  • α-D-Glucopyranuronic acid, 1→P′-ester with uridine 5′-(trihydrogen diphosphate)
  • UDP-α-D-galacturonic acid
  • 2616-64-0
  • C15H22N2O18P2
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