Uridine 5'-(trihydrogendiphosphate), P'-alpha-D-glucopyranosylester supplier

Name
Uridine 5'-(trihydrogen diphosphate), mono-alpha-d-glucopyranosyl ester
EINECS 205-121-4
CAS No. 133-89-1
Article Data67
CAS DataBase
Density 1.97 g/cm³
Solubility
Melting Point
Formula C₁₅H₂₄N₂O₁₇P₂
Boiling Point
Molecular Weight 566.306
Flash Point
Transport Information
Appearance
Safety
Risk Codes
Molecular Structure
Hazard Symbols
Synonyms Uridine5'-(trihydrogen pyrophosphate), mono-a-D-glucopyranosyl ester (8CI);Uridine 5'-pyrophosphate,a-D-glucopyranosyl ester(6CI,7CI);UDP-D-glucose;UDP-Glc;UDP-Glucose;UDP-a-D-Glucose;UDPG;Uridine 5'-(trihydrogenpyrophosphate), mono-D-glucosyl ester;Uridine 5'-(a-D-glucopyranosyl pyrophosphate);Uridine5'-diphosphate glucose;Uridine 5'-diphospho-a-D-glucose;Uridine 5'-diphosphoglucose;Uridinediphosphate glucose;Uridine diphospho-D-glucose;Uridine diphosphoglucose;Uridine pyrophosphate-glucose;
PSA 327.61000
LogP -5.40690

Synthetic route

: 63-39-8
UTP

: 59-56-3
α-D-glucopyranosyl-1-phosphate

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
With Pasteurella multocida inorganic pyrophosphatase; Bifidobacterium longumuridine 5'-diphosphate-sugarpyrophosphorylase; adenosine-5'-triphosphate; magnesium chloride In aq. buffer at 37℃; for 2h; pH=8; Enzymatic reaction;	99%
With Glucose-1-phosphate thymidylyltransferase from Streptococcus pneumonia serotype 23F; magnesium chloride at 37℃; for 1h; Enzymatic reaction;	94%
With GalU; α(1->3) galactotransferase; α(1->4) galactotransferase; manganese(ll) chloride at 37℃; for 48h; pH=7; Inert atmosphere; aq. buffer; Enzymatic reaction;	70%

: 59-56-3, 2240-08-6, 2255-14-3, 2520-52-7, 6799-01-5, 10456-01-6, 14048-34-1, 15978-07-1, 19993-19-2, 20299-62-1, 40591-51-3, 62057-78-7, 77280-79-6, 78341-19-2
glucose 1-phosphate

: 63-39-8
UTP

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
With recombinant Bifidobacterium longum ATCC55813 UDP-sugar pyrophosphorylase; recombinant Pasteurella multocida P-1059 inorganic pyrophosphatase; magnesium chloride at 37℃; for 2h; pH=8; aq. buffer; Enzymatic reaction;	99%
With yeast inorganic pyrophosphatase; recombinant Arabidopsis N-acetylglucosamine-1-phosphate uridylyltransferase-2; magnesium chloride at 37℃; for 0.166667h; pH=7.6; aq. buffer; Enzymatic reaction;

: 2280-44-6
D-Glucose

: 1476-50-2, 14264-46-1, 19817-92-6, 36051-69-1, 74674-72-9
uridine 5'-triphosphate trisodium salt

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
With pyrophosphatase, inorganic from yeast; UTP-glucose-1-phosphate galactokinase from Streptococcus pneumoniae TIGR4; UTP-glucose-1-phosphate uridylyltransferase from Streptococcus pneumoniae TIGR4; adenosine 5'-triphosphate sodium salt; magnesium chloride In aq. buffer at 42℃; for 24h; pH=8; Enzymatic reaction;	26%

: 3387-36-8
disodium uridine-5'-monophosphate

: 57-50-1
Sucrose

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
With bovine serum albumine; phospho(enol)pyruvate CHA-salt; tris hydrochloride; uridine 5'-triphosphate trisodium salt; magnesium chloride; diothiothreitol at 30℃; for 21h; sucrose synthase, pyruvate kinase, nucleoside monophosphate kinase;	21%

: 56401-20-8
α-D-Glucopyranoside 1-(disodium phosphate)

: 19817-92-6
uridine 5'-triphosphate sodium salt

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
With inorganic pyrophosphatase; uridine-5'-diphosphoglucose pyrophosphorylase enzymatically at pH 7.6;

: 299-31-0, 15209-11-7, 15209-12-8, 33163-99-4, 40436-57-5, 40436-58-6, 40436-60-0, 40436-61-1
α-D-glucose 6-phosphate

: 63-39-8
UTP

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
With phosphoglucomutase; inorganic pyrophosphatase; PAN-immobilized UDP-Glc pyrophosphorylase In water for 20h; pH 7.5;	6 mmol

: 58-98-0
UDP

: (2R,3S,4S,5R,6S)-2-Hydroxymethyl-6-(3-methoxy-pyridin-2-yloxy)-tetrahydro-pyran-3,4,5-triol

A: 133-89-1
UDP-glucose

B: 133-89-1, 2956-16-3, 7307-71-3, 7349-77-1, 16375-64-7, 16375-65-8, 16414-46-3, 17012-87-2, 25318-68-7, 78391-94-3, 99020-05-0, 99945-86-5
diphosphoric acid 1''-β-D-[1'']glucopyranosyl ester 2-(uridin-5'-yl)ester

Conditions

Conditions	Yield
In N,N-dimethyl-formamide for 190h; Ambient temperature; Yield given; Yields of byproduct given. Title compound not separated from byproducts;
In N,N-dimethyl-formamide for 3.16667h; Ambient temperature; Yield given; Yields of byproduct given. Title compound not separated from byproducts;

...Expand

: 538-75-0
dicyclohexyl-carbodiimide

pyridine salt of/the/ <5'>uridylic acid: pyridine salt of/the/ <5'>uridylic acid

pyridine salt of/the/ O1-phosphono-α-D-glucopyranose: pyridine salt of/the/ O1-phosphono-α-D-glucopyranose

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
With N,N-dimethyl-formamide; acetonitrile

...Expand

N,N'-dicyclohexyl-guanidine salt of O5'--uridine: N,N'-dicyclohexyl-guanidine salt of O5'--uridine

trioctylamine salt of/the/ O1-phosphono-α-D-glucopyranose: trioctylamine salt of/the/ O1-phosphono-α-D-glucopyranose

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
With pyridine

O2',O3'-diacetyl-O5'--uridine: O2',O3'-diacetyl-O5'--uridine

trioctylamine salt of/the/ O1-phosphono-α-D-glucopyranose: trioctylamine salt of/the/ O1-phosphono-α-D-glucopyranose

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
With tributyl-amine; benzene Hydrogenation.an Palladium/Kohle in wss. Aethanol;

O2',O3'-dibenzyl-O5'--uridine: O2',O3'-dibenzyl-O5'--uridine

trioctylamine salt of/the/ O1-phosphono-α-D-glucopyranose: trioctylamine salt of/the/ O1-phosphono-α-D-glucopyranose

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
With tributyl-amine; benzene Hydrogenation.an Palladium/Kohle in wss. Aethanol;

UDPGal: UDPGal

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
reversible enzymatische Bildung mit Hilfe von UDPglucose-4-epimerase aus Hefe;
reversible enzymatische Bildung mit Hilfe von UDPglucose-4-epimerase aus Leberextrakten;

: 59-56-3
α-D-glucopyranosyl-1-phosphate

UDPGal: UDPGal

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
reversible enzymatische Bildung mit Hilfe von Hexose-1-phosphat-uridylyltransferase aus Escherichia coli;
reversible enzymatische Bildung mit Hilfe von Hexose-1-phosphat-uridylyltransferase aus Saccharomyces fragilis;
reversible enzymatische Bildung mit Hilfe von Hexose-1-phosphat-uridylyltransferase aus Leberextrakten;

: 59-56-3
α-D-glucopyranosyl-1-phosphate

UTP: UTP

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
reversible enzymatische Bildung mit Hilfe von Glucose-1-phosphat-uridylyltransferase aus Hefe-Praeparaten;
reversible enzymatische Bildung mit Hilfe von Glucose-1-phosphat-uridylyltransferase aus Saemlingen von Phaseolus aureus;
reversible enzymatische Bildung mit Hilfe von Glucose-1-phosphat-uridylyltransferase aus Erbsen-Samen;

: 56401-20-8
α-D-Glucopyranoside 1-(disodium phosphate)

: 63-39-8
UTP

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
With thermostable inorganic pyrophosphatase; Tris buffer; UDP-glucose pyrophosphorylase from E.coli In various solvent(s) at 37℃; for 0.0833333h; pH=7.6; Enzyme kinetics; Further Variations:; Reagents;

: 58-98-0
UDP

: 57-50-1
Sucrose

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
With sucrose synthase In various solvent(s) at 37℃; for 2h; pH=6.0;
With sucrose synthase from Glycine max; potassium chloride; magnesium chloride; bovine serum albumin In dimethyl sulfoxide pH=7.5; Enzymatic reaction;
With sucrose synthase 1 Enzymatic reaction;

: 58-96-8
uridine

: 59-56-3
α-D-glucopyranosyl-1-phosphate

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
With magnesium(II); thymidylyl-transferase at 37℃; for 0.5h;

: 2956-16-3
uridine 5'-diphospho-D-galactose

: 59-56-3
α-D-glucopyranosyl-1-phosphate

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
With UDP-glucose-hexose-1-phosphate uridylyltransferase
Stage #1: uridine 5'-diphospho-D-galactose With galactose-1-phosphate uridylyltransferase for 1h; Enzymatic reaction; Stage #2: α-D-glucopyranosyl-1-phosphate Reagent/catalyst;

: 69673-09-2
cytidine-5'-phosphoro-(2-aminoimidazole)

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 1) Tri n-butylammonium pyrophosphate, 2) NaClO4 / 1) AcCN, 1 d; 2) acetone, diethyl ether 2: 95 percent / NaNO2 / acetic acid; H2O / 48 h / 4 °C 3: uridine-5'-diphosphoglucose pyrophosphorylase, inorganic pyrophosphatase / enzymatically at pH 7.6 View Scheme

: 56428-57-0
uridine 5’-monophosphate-imidazole

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 1) Tri n-butylammonium pyrophosphate, 2) NaClO4 / 1) AcCN, 1 d; 2) acetone, diethyl ether 2: uridine-5'-diphosphoglucose pyrophosphorylase, inorganic pyrophosphatase / enzymatically at pH 7.6 View Scheme

: 51450-21-6
Phosphoric acid mono-[(2R,3S,4R,5R)-5-(4-amino-2-oxo-2H-pyrimidin-1-yl)-3,4-dihydroxy-tetrahydro-furan-2-ylmethyl] ester; compound with tributyl-amine

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: acetonitrile / 24 h / 25 °C 2: 1) Tri n-butylammonium pyrophosphate, 2) NaClO4 / 1) AcCN, 1 d; 2) acetone, diethyl ether 3: 95 percent / NaNO2 / acetic acid; H2O / 48 h / 4 °C 4: uridine-5'-diphosphoglucose pyrophosphorylase, inorganic pyrophosphatase / enzymatically at pH 7.6 View Scheme

: 62540-53-8
Trioctyl-amine; compound with phosphoric acid mono-[(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3,4-dihydroxy-tetrahydro-furan-2-ylmethyl] ester

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: acetonitrile / 24 h / 25 °C 2: 1) Tri n-butylammonium pyrophosphate, 2) NaClO4 / 1) AcCN, 1 d; 2) acetone, diethyl ether 3: uridine-5'-diphosphoglucose pyrophosphorylase, inorganic pyrophosphatase / enzymatically at pH 7.6 View Scheme

: 54619-78-2
Cytidine 5'-triphosphate

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 95 percent / NaNO2 / acetic acid; H2O / 48 h / 4 °C 2: uridine-5'-diphosphoglucose pyrophosphorylase, inorganic pyrophosphatase / enzymatically at pH 7.6 View Scheme

: 63-37-6
cytidine monophosphate

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1: ethanol; methanol / 1 h / Heating 2: acetonitrile / 24 h / 25 °C 3: 1) Tri n-butylammonium pyrophosphate, 2) NaClO4 / 1) AcCN, 1 d; 2) acetone, diethyl ether 4: 95 percent / NaNO2 / acetic acid; H2O / 48 h / 4 °C 5: uridine-5'-diphosphoglucose pyrophosphorylase, inorganic pyrophosphatase / enzymatically at pH 7.6 View Scheme
Multi-step reaction with 3 steps 1: enzymatically at pH 7.5-7.8 2: 95 percent / NaNO2 / acetic acid; H2O / 48 h / 4 °C 3: uridine-5'-diphosphoglucose pyrophosphorylase, inorganic pyrophosphatase / enzymatically at pH 7.6 View Scheme

: 58-97-9
5'-Uridylic Acid

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: ethanol; methanol / 1 h / Heating 2: acetonitrile / 24 h / 25 °C 3: 1) Tri n-butylammonium pyrophosphate, 2) NaClO4 / 1) AcCN, 1 d; 2) acetone, diethyl ether 4: uridine-5'-diphosphoglucose pyrophosphorylase, inorganic pyrophosphatase / enzymatically at pH 7.6 View Scheme
Multi-step reaction with 2 steps 1: enzymatically at pH 7.6 2: uridine-5'-diphosphoglucose pyrophosphorylase, inorganic pyrophosphatase / enzymatically at pH 7.6 View Scheme

: 63-39-8
UTP

maltodextrin: maltodextrin

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
With magnesium chloride at 30℃; for 10h; pH=7.5; aq. phosphate buffer; Enzymatic reaction;	Ca. 630 mg

: 99-20-7
TREHALOSE

: 58-98-0
UDP

A: 133-89-1
UDP-glucose

B: 50-99-7
D-glucose

Conditions

Conditions	Yield
With Pyrococcus horikoshii trehalose synthase at 60℃; for 24h; pH=6; Kinetics; Time; aq. acetate buffer; Enzymatic reaction;

...Expand

: 528-04-1, 2616-63-9, 7277-98-7, 16465-33-1, 19014-00-7, 26234-54-8, 26575-17-7, 27963-82-2, 29217-44-5, 125639-14-7
uridine-5'-diphospho-N-acetyl-D-galactosamine

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: pyrophosphate tetraanion; recombinant Arabidopsis N-acetylglucosamine-1-phosphate uridylyltransferase-1; magnesium chloride / 0.17 h / 37 °C / pH 7.6 / aq. buffer; Enzymatic reaction 2: yeast inorganic pyrophosphatase; recombinant Arabidopsis N-acetylglucosamine-1-phosphate uridylyltransferase-2; magnesium chloride / 0.17 h / 37 °C / pH 7.6 / aq. buffer; Enzymatic reaction View Scheme

Yield

Multi-step reaction with 2 steps
1: pyrophosphate tetraanion; recombinant Arabidopsis N-acetylglucosamine-1-phosphate uridylyltransferase-1; magnesium chloride / 0.17 h / 37 °C / pH 7.6 / aq. buffer; Enzymatic reaction
2: yeast inorganic pyrophosphatase; recombinant Arabidopsis N-acetylglucosamine-1-phosphate uridylyltransferase-2; magnesium chloride / 0.17 h / 37 °C / pH 7.6 / aq. buffer; Enzymatic reaction
View Scheme

: 2280-44-6
D-Glucose

: 63-39-8
UTP

: 133-89-1
UDP-glucose

Conditions

Conditions	Yield
With pyrophosphatase; Streptococcus pneumoniae TIGR4 galactokinase; Arabidopsis thaliana uridine-diphosphate-sugar pyrophosphorylase; ATP; magnesium chloride In aq. buffer at 42℃; for 1h; pH=8; Enzymatic reaction;
With rabbit muscle phosphoglucomutase; S. cerevisiae hexokinase; S. cerevisiae inorganic pyrophosphatase; UTP-glucose-1-phosphate uridylyltransferase from Bifidobacterium longum subsp. longum JCM 1217; magnesium chloride; bovine serum albumin; 6-phospho-α-D-glucopyranosyl-1-phosphate In aq. buffer at 30℃; for 24h; pH=7.5; Enzymatic reaction;

: 133-89-1
UDP-glucose

sodium N4-[2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->2)-α-D-mannopyranosyl-(1->3)-(2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6))-β-D-mannopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl]-L-asparaginate: sodium N4-[2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->2)-α-D-mannopyranosyl-(1->3)-(2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6))-β-D-mannopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl]-L-asparaginate

sodium N4-[β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->2)-α-D-mannopyranosyl-(1->3)-(β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6))-β-D-mannopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl]-L-asparaginate: sodium N4-[β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->2)-α-D-mannopyranosyl-(1->3)-(β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6))-β-D-mannopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl]-L-asparaginate

Conditions

Conditions	Yield
With bacterial β1-4-galactosyltransferase/UDP-4-Gal-epimerase fusion protein; manganese(ll) chloride at 37℃; pH=7.5; aq. buffer; Enzymatic reaction;	100%

: 133-89-1
UDP-glucose

sodium N4-[2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->2)-α-D-mannopyranosyl-(1->3)-(2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6))-β-D-mannopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl]-L-asparaginate: sodium N4-[2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->2)-α-D-mannopyranosyl-(1->3)-(2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6))-β-D-mannopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl]-L-asparaginate

sodium N4-[β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->2)-α-D-mannopyranosyl-(1->3)-(β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6))-β-D-mannopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl]-L-asparaginate: sodium N4-[β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->2)-α-D-mannopyranosyl-(1->3)-(β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6))-β-D-mannopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl]-L-asparaginate

Conditions

Conditions	Yield
With bacterial β1-4-galactosyltransferase/UDP-4-Gal-epimerase fusion protein; manganese(ll) chloride at 37℃; pH=7.5; aq. buffer; Enzymatic reaction;	100%

: 133-89-1
UDP-glucose

: C28H47N4O18(1-)*Na(1+)

: sodium O3-[β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-(β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->6))-2-acetamido-2-deoxy-D-galactopyranosyl]-L-threonate

Conditions

Conditions	Yield
With CIAP; bacterial β1-4-galactosyltransferase/UDP-4-Gal-epimerase fusion protein; manganese(ll) chloride at 37℃; pH=7.5; aq. buffer; Enzymatic reaction;	100%

: 133-89-1
UDP-glucose

: sodium O3-[2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-(2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->6))-2-acetamido-2-deoxy-D-galactopyranosyl]-L-threonate

: sodium O3-[β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-(β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->6))-2-acetamido-2-deoxy-D-galactopyranosyl]-L-threonate

Conditions

Conditions	Yield
With CIAP; bacterial β1-4-galactosyltransferase/UDP-4-Gal-epimerase fusion protein; manganese(ll) chloride at 37℃; pH=7.5; aq. buffer; Enzymatic reaction;	100%

: 133-89-1
UDP-glucose

: sodium O3-[2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->6)-(β-D-galactopyranosyl-(1->3))-2-acetamido-2-deoxy-D-galactopyranosyl]-L-threonate

: sodium O3-[β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->6)-(β-D-galactopyranosyl-(1->3))-2-acetamido-2-deoxy-D-galactopyranosyl]-L-threonate

Conditions

Conditions	Yield
With CIAP; bacterial β1-4-galactosyltransferase/UDP-4-Gal-epimerase fusion protein; manganese(ll) chloride at 37℃; pH=7.5; aq. buffer; Enzymatic reaction;	100%

: 133-89-1
UDP-glucose

: C20H34N3O13(1-)*Na(1+)

: sodium O3-[β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-2-acetamido-2-deoxy-D-galactopyranosyl]-L-threonate

Conditions

Conditions	Yield
With CIAP; bacterial β1-4-galactosyltransferase/UDP-4-Gal-epimerase fusion protein; manganese(ll) chloride at 37℃; pH=7.5; aq. buffer; Enzymatic reaction;	100%

: 133-89-1
UDP-glucose

: 60-82-2
3-(4-Hydroxy-phenyl)-1-(2,4,6-trihydroxy-phenyl)-propan-1-on

: 1-[3-(β-D-glucopyranosyl)-2,4,6-trihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one

Conditions

Conditions	Yield
With C-glycosyltransferase from Mangifera indica In methanol at 40℃; for 12h; pH=6.6; Enzymatic reaction;	100%
With c-glycosyltransferase from oryza sativa; potassium chloride; magnesium chloride; bovine serum albumin In dimethyl sulfoxide at 30℃; pH=7.5; Enzymatic reaction;
With Mangifera indica C-glycosyltransferase for 12h; Enzymatic reaction; stereospecific reaction;	2.2 mg
With c-glycosyltransferase from oryza sativa; potassium chloride; magnesium chloride In dimethyl sulfoxide at 30℃; pH=7.5; Enzymatic reaction;

: 133-89-1
UDP-glucose

: 3-(2',4',6'-trihydroxybenzoyl)pyridine

: 3-(3'-(C-β-D-glucosyl)-2',4',6'-trihydroxybenzoyl)-pyridine

Conditions

Conditions	Yield
With C-glycosyltransferase from Mangifera indica In methanol at 40℃; for 12h; pH=6.6; Enzymatic reaction;	100%
With Mangifera indica C-glycosyltransferase for 12h; Enzymatic reaction; stereospecific reaction;	2.5 mg

: 133-89-1
UDP-glucose

: (2,4,6-trihydroxyphenyl)(thienyl-2')methanone

: (3-(C-β-D-glucosyl)-2,4,6-trihydroxyphenyl)(thienyl-2')methanone

Conditions

Conditions	Yield
With C-glycosyltransferase from Mangifera indica In methanol at 40℃; for 12h; pH=6.6; Enzymatic reaction;	100%
With Mangifera indica C-glycosyltransferase for 12h; Enzymatic reaction; stereospecific reaction;	10.6 mg

: 133-89-1
UDP-glucose

: (2,4,6-trihydroxyphenyl) (naphthyl-2')methanone

: (3-(C-β-D-glucosyl)-2,4,6-trihydroxyphenyl)(naphthyl-2')methanone

Conditions

Conditions	Yield
With C-glycosyltransferase from Mangifera indica In methanol at 40℃; for 12h; pH=6.6; Enzymatic reaction;	100%
With Mangifera indica C-glycosyltransferase for 12h; Enzymatic reaction; stereospecific reaction;	1.8 mg

: 133-89-1
UDP-glucose

: 519-34-6
maclurin

: 92631-83-9
3-glucosyl-2,3′,4,4′,6-pentahydroxybenzophenone

Conditions

Conditions	Yield
With C-glycosyltransferase from Mangifera indica In methanol at 40℃; for 12h; pH=6.6; Enzymatic reaction;	100%
With Mangifera indica C-glycosyltransferase for 12h; Kinetics; Enzymatic reaction; stereospecific reaction;	4.3 mg
With recombinant di‑C‑glycosyltransferase from Glycyrrhiza glabra In aq. phosphate buffer at 37℃; for 2h; pH=8; Enzymatic reaction;

: 133-89-1
UDP-glucose

: 3555-86-0
2-benzoylphloroglucinol

: phlorobenzophenone 3-C-β-D-glucoside

Conditions

Conditions	Yield
With C-glycosyltransferase from Mangifera indica In methanol at 40℃; for 12h; pH=6.6; Enzymatic reaction;	100%
With Mangifera indica C-glycosyltransferase for 12h; Enzymatic reaction; stereospecific reaction;	4.5 mg

: 133-89-1
UDP-glucose

: 26271-33-0
(3-hydroxyphenyl)(2,4,6-trihydroxyphenyl)methanone

: 3-(C-β-D-glucosyl)-2,3',4,6-tetrahydroxybenzophenone

Conditions

Conditions	Yield
With C-glycosyltransferase from Mangifera indica In methanol at 40℃; for 12h; pH=6.6; Enzymatic reaction;	100%
With Mangifera indica C-glycosyltransferase for 12h; Enzymatic reaction; stereospecific reaction;	8 mg

: 133-89-1
UDP-glucose

: 727-71-9
2-phenyl-2',4',6'-trihydroxyacetophenone

: 1-[3-(β-D-glucopyranosyl)-2,4,6-trihydroxyphenyl]-2-phenylethan-1-one

Conditions

Conditions	Yield
With C-glycosyltransferase from Mangifera indica In methanol at 40℃; for 12h; pH=6.6; Enzymatic reaction;	100%
With Mangifera indica C-glycosyltransferase for 12h; Enzymatic reaction; stereospecific reaction;	11.7 mg

: 133-89-1
UDP-glucose

: 131-56-6
2,4-dihydroxybenzophenone

: C19H20O8

Conditions

Conditions	Yield
With C-glycosyltransferase from Mangifera indica In methanol at 40℃; for 12h; pH=6.6; Enzymatic reaction;	100%

: 133-89-1
UDP-glucose

: 39731-47-0
gentisein

: C19H18O10

Conditions

Conditions	Yield
With C-glycosyltransferase from Mangifera indica In methanol at 40℃; for 12h; pH=6.6; Enzymatic reaction;	100%

: 133-89-1
UDP-glucose

: 105904-53-8
xanthene-1,3,6,7-tetraol

: C19H20O10

Conditions

Conditions	Yield
With C-glycosyltransferase from Mangifera indica In methanol at 40℃; for 12h; pH=6.6; Enzymatic reaction;	100%

: 133-89-1
UDP-glucose

: 52591-10-3
4,2',4',6'-tetrahydroxybenzophenone

: 104669-02-5
2,4,4',6-tetrahydroxy benzophenone-3-C-β-D-glucoside

Conditions

Conditions	Yield
With C-glycosyltransferase from Mangifera indica In methanol at 40℃; for 12h; pH=6.6; Enzymatic reaction;	100%

: 133-89-1
UDP-glucose

: 81520-71-0, 81520-72-1, 16334-31-9
penta-N-acetylchitopentaose

: C46H77N5O31

Conditions

Conditions	Yield
With cacodylate buffer; manganese(ll) chloride at 30℃; for 48h; pH=7.5;	98%

: 133-89-1
UDP-glucose

: 142072-12-6
2'-azidoethyl 2-acetamido-2-deoxy-β-D-glucopyranoside

: 338971-38-3
2-azidoethyl (β-D-galactopyranosyl)-(1->4)-O-2-acetamido-2-deoxy-β-D-glucopyranoside

Conditions

Conditions	Yield
With β-(1->4)-galactosyltransferase; UDP-galactose 4'-epimerase; sodium cacodylate; manganese(ll) chloride In water at 20℃; for 24h; pH=7.5;	96%

: 133-89-1
UDP-glucose

: 66346-59-6
5,7-dihydroxy-4-propylcoumarin

: 6-(C-β-D-glucosyl)-4-propyl-5,7-dihydroxycoumarin

Conditions

Conditions	Yield
With whole E. coli cells harboring MiCGTb-GAGM In aq. phosphate buffer at 30℃; for 24h; pH=8;	95.6%

: 133-89-1
UDP-glucose

: 18404-72-3
benzyl 4-O-β-D-galactopyranosyl-β-D-glucopyranoside

: 330203-79-7
benzyl α-D-galactopyranosyl-(1->3)-β-D-galactopyranosyl-(1->)4-β-D-glucopyranoside

Conditions

Conditions	Yield
With hydrogenchloride; Escherichia coli K12 UPD-Glc GalE C4 epimerase; Neisseria meningitidis LgtC α1,4-galactosyltransferase; 2-amino-2-hydroxymethyl-1,3-propanediol; manganese(ll) chloride; D,L-dithiothreitol In water; glycerol at 20℃; for 48h; pH=7.5; Enzymatic reaction;	90%

: 133-89-1
UDP-glucose

: 133-99-3, 490-37-9, 2152-98-9, 4482-75-1, 5965-66-2, 13299-27-9, 13360-52-6, 14641-93-1, 15548-43-3, 16462-44-5, 16984-36-4, 16984-38-6, 20869-27-6, 22688-72-8, 27452-49-9, 29276-55-9, 30608-12-9, 34481-13-5, 37169-60-1, 37169-64-5, 64234-01-1, 64234-02-2, 75281-88-8, 80446-85-1, 84413-57-0, 92344-56-4, 93221-87-5, 93301-77-0, 94799-29-8, 100427-98-3, 100428-00-0, 101312-82-7, 102046-24-2, 102046-25-3, 109432-00-0, 109432-02-2, 109432-04-4, 109432-08-8, 135268-49-4, 138231-26-2, 140461-59-2, 145414-22-8, 145414-26-2, 146339-75-5, 146339-76-6, 149116-55-2
Lactose

: C18H32O16

Conditions

Conditions	Yield
With α(1->4) galactotransferase; GAlE epimerase; manganese(ll) chloride at 37℃; for 48h; pH=7; Inert atmosphere; aq. buffer; Enzymatic reaction;	90%

: 133-89-1
UDP-glucose

: 465-39-4, 24183-15-1, 35495-98-8, 36121-79-6, 62859-81-8
resibufogenin

: resibufogenin 3-O-β-D-glucoside

Conditions

Conditions	Yield
With Bacillus subtilis glycosyltransferase YjiC1 In dimethyl sulfoxide at 37℃; for 12h; pH=8.0; Enzymatic reaction;	90%
With UGT74AN1; magnesium chloride In aq. buffer at 37℃; for 12h; pH=8; Enzymatic reaction;	4.5 mg

: 133-89-1
UDP-glucose

: 464-74-4
adrenobufagin

: arenobufagin 3-O-β-D-glucoside

Conditions

Conditions	Yield
With Bacillus subtilis glycosyltransferase YjiC1 In dimethyl sulfoxide at 37℃; for 12h; pH=8.0; Enzymatic reaction;	90%
With UGT74AN1; magnesium chloride In aq. buffer at 37℃; for 12h; pH=8; Enzymatic reaction;	5.6 mg

: 133-89-1
UDP-glucose

: 188583-24-6
phenyl 2-deoxy-1-thio-2-(2,2,2-trichloroethoxycarbonylamino)-β-D-glucopyranoside

: 512174-10-6
phenyl O-(β-D-galactopyranosyl)-(1-4)-2-deoxy-1-thio-2-(2,2,2-trichloroethoxycarbonylamino)-β-D-glucopyranoside

Conditions

Conditions	Yield
With UDP-galactose 4-epimerase; β(1-4)galactosyltransferase; manganese(ll) chloride In various solvent(s) at 37℃; for 20h; pH=7.4; Enzymatic reaction;	89%

: 133-89-1
UDP-glucose

: C26H44N3O18(1-)*Na(1+)

: sodium O3-[β-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->6)-(β-D-galactopyranosyl-(1->3))-2-acetamido-2-deoxy-D-galactopyranosyl]-L-threonate

Conditions

Conditions	Yield
With CIAP; bacterial β1-4-galactosyltransferase/UDP-4-Gal-epimerase fusion protein; manganese(ll) chloride at 37℃; pH=7.5; aq. buffer; Enzymatic reaction;	89%

: 133-89-1
UDP-glucose

: 135-19-3
β-naphthol

: 6044-30-0
naphthyl-beta-D-glucopyranoside

Conditions

Conditions	Yield
With Aloearborescensglycosyltransferase*GT3 In dimethyl sulfoxide at 30℃; for 12h; pH=7.4; Enzymatic reaction;	89%

Uridine 5'-(trihydrogendiphosphate), P'-alpha-D-glucopyranosylester Specification

The Uridine 5'-(trihydrogendiphosphate), P'-alpha-D-glucopyranosylester is an organic compound with the formula C₁₅H₂₄N₂O₁₇P₂. The systematic name of this chemical is [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl (2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl dihydrogen diphosphate ( non-preferred name). With the CAS registry number 133-89-1, it is also named as Uridine 5'-Pyrophosphate Glucose Ester.

Physical properties about Uridine 5'-(trihydrogendiphosphate), P'-alpha-D-glucopyranosylester are: (1)ACD/LogP: -4.51; (2)# of Rule of 5 Violations: 3; (3)ACD/LogD (pH 5.5): -9.01; (4)ACD/LogD (pH 7.4): -9.06; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 1; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 19; (10)#H bond donors: 9; (11)#Freely Rotating Bonds: 15; (12)Polar Surface Area: 214.37 Å²; (13)Index of Refraction: 1.673; (14)Molar Refractivity: 107.32 cm³; (15)Molar Volume: 286.2 cm3; (16)Polarizability: 42.54×10^-24cm³; (17)Surface Tension: 125 dyne/cm; (18)Density: 1.97 g/cm³.

You can still convert the following datas into molecular structure:
(1)SMILES: O=P(O[C@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)CO)(O)OP(=O)(O)OC[C@H]3O[C@@H](N2/C=C\C(=O)NC2=O)[C@H](O)[C@@H]3O
(2)InChI: InChI=1/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
(3)InChIKey: HSCJRCZFDFQWRP-JZMIEXBBBU
(4)Std. 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
(5)Std. InChIKey: HSCJRCZFDFQWRP-JZMIEXBBSA-N

Product Name

Uridine 5'-(trihydrogen diphosphate), mono-alpha-d-glucopyranosyl ester

Synthetic route

Uridine 5'-(trihydrogendiphosphate), P'-alpha-D-glucopyranosylester Specification

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