Product Name

  • Name

    Uridine 5'-triphosphate

  • EINECS 200-558-7
  • CAS No. 63-39-8
  • Article Data48
  • CAS DataBase
  • Density 2.106 g/cm3
  • Solubility
  • Melting Point
  • Formula C9H15N2O15P3
  • Boiling Point
  • Molecular Weight 484.144
  • Flash Point 113oC
  • Transport Information
  • Appearance
  • Safety 22-26-36
  • Risk Codes 20/21/22-68/20/21/22
  • Molecular Structure Molecular Structure of 63-39-8 (Uridine 5'-triphosphate)
  • Hazard Symbols HarmfulXn
  • Synonyms Magnesium Uridine Triphosphate;Magnesium UTP;Mg UTP;Mg-UTP;Triphosphate, Magnesium Uridine;Triphosphate, Uridine;Uridine Triphosphate;UTP;UTP, Magnesium
  • PSA 293.80000
  • LogP -2.50090

Synthetic route

5'-Uridylic Acid
58-97-9

5'-Uridylic Acid

A

UDP
58-98-0

UDP

B

UTP
63-39-8

UTP

Conditions
ConditionsYield
With N-ethylmorpholine buffer; phosphorotriimidazolide at 22℃; for 72h; other 5'-nucleotides, also with phosphorotribenzimidazolide, MnCl2; other time, temperature;A 25%
B 36%
With phosphorotriimidazolide; magnesium chloride at 22℃; for 72h; N-ethylmorpholine buffer (pH 7.0);A 25%
B 36%
C9H14N2O16P4

C9H14N2O16P4

Conditions
ConditionsYield
With pyridine; water; iodine In N,N-dimethyl-formamide at 20℃; for 2.25h;9.3%
orotic acid
65-86-1

orotic acid

Conditions
ConditionsYield
durch Biosynthese;
5'-Uridylic Acid
58-97-9

5'-Uridylic Acid

Conditions
ConditionsYield
reversible enzymatische Bildung mit Hilfe von wss. Nucleosidmonophosphat-kinase aus Hefe-Praeparaten;
reversible enzymatische Bildung mit Hilfe von wss. Nucleosidmonophosphat-kinase aus Leber-Praeparaten;
reversible enzymatische Bildung mit Hilfe von wss. Nucleosidmonophosphat-kinase aus Erbsen-Samen;
uridine 5'-(2-deoxy-α-D-glucopyranosyl diphosphate)
13491-28-6, 13529-36-7, 28196-62-5, 65309-82-2, 18521-38-5

uridine 5'-(2-deoxy-α-D-glucopyranosyl diphosphate)

A

2-deoxy-α-D-glucopyranosyl
42400-47-5

2-deoxy-α-D-glucopyranosyl

B

UTP
63-39-8

UTP

Conditions
ConditionsYield
With sodium pyrophosphate; uridine-5'-diphosphoglucose pyrophosohorylase; 2-amino-2-hydroxymethyl-1,3-propanediol; magnesium chloride; bovine serum albumin In water at 25℃; for 72h;
Conditions
ConditionsYield
With UDPG pyrophosphorylase In water at 25℃; for 4h; Equilibrium constant; pH 7.2;
Conditions
ConditionsYield
With polyphosphate; Escherichia coli polyphosphate kinase; tris hydrochloride In water at 37℃; for 16h;49.6 % Chromat.
With rabbit muscle pyruvate kinase; potassium chloride; phosphoenolpyruvic acid; D,L-dithiothreitol at 20℃; pH=7.5; Kinetics; Concentration; Reagent/catalyst; Tris buffer;
O5'-<2-α-D-glucopyranosyl-1,2-dihydroxy-diphosphoryl>-uridine

O5'-<2-α-D-glucopyranosyl-1,2-dihydroxy-diphosphoryl>-uridine

Conditions
ConditionsYield
With pyrophosphoric acid mit Hilfe von Glucose-1-phosphat-uridylyltransferase;
O5'--O2',O3'-isopropyliden-uridine

O5'--O2',O3'-isopropyliden-uridine

tetramethylammonium salt of diphosphoric acid-tribenzyl ester

tetramethylammonium salt of diphosphoric acid-tribenzyl ester

Conditions
ConditionsYield
With acetonitrile anschl. mit m-Kresol und anschl. Hydrieren an Palladium/Kohle in wss. Aethanol und Behandeln mit wss. LiOH;
phosphoenolpyruvic acid
138-08-9

phosphoenolpyruvic acid

UDP

UDP

Conditions
ConditionsYield
durch enzymatische Bildung mit Hilfe von Pyruvatkinase aus Kaninchenmuskelgewebe;
UDP

UDP

Conditions
ConditionsYield
reversible enzymatische Bildung mit Hilfe von wss. Nucleosiddiphosphat-kinase aus Hefe-Praeparaten und tierischen Gewebeextrakten;
reversible enzymatische Bildung mit Hilfe von wss. Nucleosiddiphosphat-kinase aus Erbsen-Samen;
yeast RNA

yeast RNA

A

guanosine 5'-triphosphate
86-01-1

guanosine 5'-triphosphate

B

cytidine triphosphate
65-47-4

cytidine triphosphate

C

UTP
63-39-8

UTP

D

ATP
56-65-5

ATP

Conditions
ConditionsYield
With sodium hydroxide; potassium phosphate; nuclease P1; PAN-immobilized PNPase; phospho(enol)pyruvic acid mono potassium salt; magnesium chloride; manganese(ll) chloride 1.) water, 50 deg C, 1 h, 2.) room temperature, 4 days; Yield given. Multistep reaction. Yields of byproduct given;
ribonucleic acid

ribonucleic acid

A

UTP
63-39-8

UTP

B

other nucleotides

other nucleotides

Conditions
ConditionsYield
With magnesium oxide at 140 - 145℃; in wss. Loesung (pH 8 -8.5) und Behandeln des Nucleosid-Gemisches in wss. Loesung (pH ca. 7) in Gegenwart von Hefe und Dextrose mit NaH2PO4 und Na2HPO4;
5'-Uridylic Acid
58-97-9

5'-Uridylic Acid

dicyclohexyl-carbodiimide
538-75-0

dicyclohexyl-carbodiimide

A

UTP
63-39-8

UTP

B

UDP

UDP

Conditions
ConditionsYield
With pyridine; tributyl-amine; phosphoric acid
With pyridine; phosphoric acid
C14H22N3O8P

C14H22N3O8P

Conditions
ConditionsYield
With tris(tetra-n-butylammonium) hydrogen pyrophosphate In tetrahydrofuran at 20℃; for 0.5h;45 mg
2',3'-O-(methoxymethylidene)uridine
16628-81-2

2',3'-O-(methoxymethylidene)uridine

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1: 690 mg / N-methylimidazole; pyridine / tetrahydrofuran / 20 °C
2: LiHMDS / tetrahydrofuran / 2 h / -78 - 0 °C
3: 215 mg / aq. HCl / acetonitrile / 4 h / 20 °C / pH 2.0
4: H2 / Pd/C / tetrahydrofuran / 2 h / 20 °C
5: 45 mg / tris(tetra-n-butylammonium) hydrogen pyrophosphate / tetrahydrofuran / 0.5 h / 20 °C
View Scheme
(4-Chloro-butyl)-methyl-phosphoramidic acid benzyl ester (3aR,4R,6R,6aR)-6-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-2-methoxy-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester

(4-Chloro-butyl)-methyl-phosphoramidic acid benzyl ester (3aR,4R,6R,6aR)-6-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-2-methoxy-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 215 mg / aq. HCl / acetonitrile / 4 h / 20 °C / pH 2.0
2: H2 / Pd/C / tetrahydrofuran / 2 h / 20 °C
3: 45 mg / tris(tetra-n-butylammonium) hydrogen pyrophosphate / tetrahydrofuran / 0.5 h / 20 °C
View Scheme
5'-uridyl benzyl N-methyl-N-(4-chlorobutyl)phosphoramidate
727398-81-4

5'-uridyl benzyl N-methyl-N-(4-chlorobutyl)phosphoramidate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: H2 / Pd/C / tetrahydrofuran / 2 h / 20 °C
2: 45 mg / tris(tetra-n-butylammonium) hydrogen pyrophosphate / tetrahydrofuran / 0.5 h / 20 °C
View Scheme
(4-Chloro-butyl)-methyl-phosphoramidic acid benzotriazol-1-yl ester (3aR,4R,6R,6aR)-6-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-2-methoxy-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester
727399-01-1

(4-Chloro-butyl)-methyl-phosphoramidic acid benzotriazol-1-yl ester (3aR,4R,6R,6aR)-6-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-2-methoxy-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: LiHMDS / tetrahydrofuran / 2 h / -78 - 0 °C
2: 215 mg / aq. HCl / acetonitrile / 4 h / 20 °C / pH 2.0
3: H2 / Pd/C / tetrahydrofuran / 2 h / 20 °C
4: 45 mg / tris(tetra-n-butylammonium) hydrogen pyrophosphate / tetrahydrofuran / 0.5 h / 20 °C
View Scheme
2',3'-O-isopropylideneuridine
362-43-6

2',3'-O-isopropylideneuridine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: pyridine; chlorophosphoric acid dibenzyl ester / -40 - -30 °C / anschl. Hydrierung
2: aqueous H3PO4; aqueous pyridine
View Scheme
C9H11Cl2N2O7P

C9H11Cl2N2O7P

A

5'-Uridylic Acid
58-97-9

5'-Uridylic Acid

B

UTP
63-39-8

UTP

Conditions
ConditionsYield
With tributyl-amine; bis(tri-n-butylammonium) pyrophosphate In N,N-dimethyl-formamide at -15℃; for 2h;A n/a
B 107 mg
uridine
58-96-8

uridine

A

5'-Uridylic Acid
58-97-9

5'-Uridylic Acid

B

UTP
63-39-8

UTP

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: trichlorophosphate / trimethyl phosphite / 2 h / -15 °C
2: tributyl-amine; bis(tri-n-butylammonium) pyrophosphate / N,N-dimethyl-formamide / 2 h / -15 °C
View Scheme
Conditions
ConditionsYield
With pyrophosphate tetraanion; recombinant Arabidopsis N-acetylglucosamine-1-phosphate uridylyltransferase-1; magnesium chloride at 37℃; for 0.166667h; pH=7.6; Kinetics; Concentration; Reagent/catalyst; aq. buffer; Enzymatic reaction;

A

N-acetylgalactosamine-1-phosphate

N-acetylgalactosamine-1-phosphate

B

UTP
63-39-8

UTP

Conditions
ConditionsYield
With pyrophosphate tetraanion; recombinant Arabidopsis N-acetylglucosamine-1-phosphate uridylyltransferase-1; magnesium chloride at 37℃; for 0.166667h; pH=7.6; Kinetics; Reagent/catalyst; Concentration; aq. buffer; Enzymatic reaction;
uridine
58-96-8

uridine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: N,N-dimethyl-formamide / 1.5 h / 20 °C / Inert atmosphere
2: pyridine; iodine; water / N,N-dimethyl-formamide / 2.25 h / 20 °C
View Scheme
α-D-glucopyranosyl-1-phosphate
59-56-3

α-D-glucopyranosyl-1-phosphate

UDP-glucose
133-89-1

UDP-glucose

Conditions
ConditionsYield
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%
N-azidoacetylgalactosamine

N-azidoacetylgalactosamine

5’-diphospho-2-azidoacetamido galactosamine

5’-diphospho-2-azidoacetamido galactosamine

Conditions
ConditionsYield
With recombinant human GalNAc kinase GK2; recombinant human UDP-GalNAc pyrophosphorylase AGX1; ATP; yeast inorganic pyrophosphatase In various solvent(s) at 37℃; pH=8.8;99%
Conditions
ConditionsYield
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;
Conditions
ConditionsYield
With yeast inorganic pyrophosphatase; N-acetylglucosamine-1-phosphate pyrophosphorylase from C. jejuni NCTC 11168; tris hydrochloride; magnesium chloride at 37℃; for 2h; pH=7.5;97.9%
With Pyrococcus furiosus enzyme; magnesium(II) In various solvent(s) at 80℃; pH=7.5; Enzyme kinetics;
With Pyrococcus furious enzyme; magnesium(II) In various solvent(s) at 80℃; for 1h; pH=7.5;
2-trifluoroacetamido-2-deoxy-α,β-D-glucopyranose
667462-08-0

2-trifluoroacetamido-2-deoxy-α,β-D-glucopyranose

uridine 5'-diphospho-2-deoxy-2-trifluoroacetamido-α-D-glucopyranoside
212137-54-7

uridine 5'-diphospho-2-deoxy-2-trifluoroacetamido-α-D-glucopyranoside

Conditions
ConditionsYield
With inorganic pyrophosphatase cloned from Pasteurella multocida strain P-1059; N-acetylglucosamine-1-phosphate uridylyltransferase cloned from Pasteurella multocida strain P-1059 (ATCC15742); N-acetylhexosamine 1-kinase cloned from Bifidobacterium longum ATCC55813; ATP; magnesium chloride In water at 37℃; pH=8; aq. buffer; Enzymatic reaction;97%
With hydrogenchloride; N-acetylglucosamine-1-phosphate uridylyltransferase from Escherichia coli K12 MG1655; pyrophosphatase from Escherichia coli K12 MG1655; recombinant N-acetylhexosamine 1-kinase; ATP; magnesium chloride In aq. buffer at 37℃; pH=8.5; Concentration; Temperature; pH-value; Enzymatic reaction;
With inorganic pyrophosphatase from P. multocida; N-acetyl hexosamine 1-kinase from Bifidobacterium infantis; UDP-N-acetylgalactosamine pyrophosphorylase from Pasteurella multocida; ATP; sodium hydroxide; magnesium chloride In aq. buffer at 37℃; for 24h; pH=7; Enzymatic reaction;
ammonium 2-acetamido-2,6-dideoxy-6-fluoro-α-D-glucopyranosyl-1-phosphate

ammonium 2-acetamido-2,6-dideoxy-6-fluoro-α-D-glucopyranosyl-1-phosphate

uridine 5'-diphospho-2-acetamido-2,6-dideoxy-6-fluoro-α-D-glucopyranose diammonium salt

uridine 5'-diphospho-2-acetamido-2,6-dideoxy-6-fluoro-α-D-glucopyranose diammonium salt

Conditions
ConditionsYield
With pyrophosphatase from C. cerevisiae; uridyl transferase GlmU from E. coli K12; magnesium chloride In aq. buffer at 37℃; for 24h; pH=7.5; Enzymatic reaction;95%
ammonium 2-acetamido-2,6-dideoxy-6-thio-α-D-glucopyranosyl-1-phosphate

ammonium 2-acetamido-2,6-dideoxy-6-thio-α-D-glucopyranosyl-1-phosphate

uridine 5'-diphospho-2-acetamido-2,6-dideoxy-6-thio-α-D-glucopyranose diammonium salt

uridine 5'-diphospho-2-acetamido-2,6-dideoxy-6-thio-α-D-glucopyranose diammonium salt

Conditions
ConditionsYield
With pyrophosphatase from C. cerevisiae; uridyl transferase GlmU from E. coli K12; magnesium chloride; D,L-dithiothreitol In aq. buffer at 37℃; for 24h; pH=7.5; Enzymatic reaction;93%
Conditions
ConditionsYield
With recombinant Bifidobacterium infantis ATCC15697 N-acetylhexosamine 1-kinase; recombinant Bifidobacterium longum ATCC55813 UDP-sugar pyrophosphorylase; recombinant Pasteurella multocida P-1059 inorganic pyrophosphatase; ATP; magnesium chloride at 37℃; for 24h; pH=8; aq. buffer; Enzymatic reaction;92%
2-deoxy-2-trifluoroacetamido-5-thio-D-glucose

2-deoxy-2-trifluoroacetamido-5-thio-D-glucose

C17H24F3N3O16P2S

C17H24F3N3O16P2S

Conditions
ConditionsYield
With ATP; magnesium chloride In aq. buffer at 37℃; for 36h;92%
Conditions
ConditionsYield
With inorganic pyrophosphatase; recombinant thymidylyltransferase from Aneurinibacillus thermoaerophilus DSM 10155; magnesium chloride at 55℃; for 1.5h; pH=7.5; Inert atmosphere; aq. buffer; Enzymatic reaction;90%
With Glucose-1-phosphate thymidylyltransferase from Streptococcus pneumonia serotype 23F for 48h; Enzymatic reaction;86%
With phosphate buffer; UDPG-PPase from Pyrococcus furiosus DSM 3638 at 90℃; pH=7.5; Enzyme kinetics;
2-azido-2-deoxy-D-mannopyranose
97604-58-5

2-azido-2-deoxy-D-mannopyranose

uridine 5'-diphospho-2-azido-2-deoxy-α-D-mannopyranoside
1363386-22-4

uridine 5'-diphospho-2-azido-2-deoxy-α-D-mannopyranoside

Conditions
ConditionsYield
With recombinant Bifidobacterium infantis ATCC15697 N-acetylhexosamine 1-kinase; recombinant Bifidobacterium longum ATCC55813 UDP-sugar pyrophosphorylase; recombinant Pasteurella multocida P-1059 inorganic pyrophosphatase; ATP; magnesium chloride at 37℃; for 24h; pH=8; aq. buffer; Enzymatic reaction;90%
D-glucuronic acid
70021-34-0

D-glucuronic acid

UDP-glucuronic acid
2616-64-0

UDP-glucuronic acid

Conditions
ConditionsYield
With glucuronokinase from Arabidopsis thaliana; pyrophosphatase from E. coli; UDP-sugar pyrophosphorylasegene from Arabidopsis thaliana; ATP; magnesium chloride In aq. buffer at 37℃; pH=8; Enzymatic reaction;89%
D-Galactose
10257-28-0

D-Galactose

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

uridine 5'-diphospho-D-galactose

Conditions
ConditionsYield
With recombinant Bifidobacterium longum ATCC55813 UDP-sugar pyrophosphorylase; recombinant Escherichia coli K-12 galactokinase; recombinant Pasteurella multocida P-1059 inorganic pyrophosphatase; ATP; magnesium chloride at 37℃; for 24h; pH=8; aq. buffer; Enzymatic reaction;86%
With Pasteurella multocida inorganic pyrophosphatase; Bifidobacterium longumuridine 5'-diphosphate-sugarpyrophosphorylase; Echerichia coli galactokinase; adenosine-5'-triphosphate; magnesium chloride In aq. buffer at 37℃; for 24h; pH=8; Reagent/catalyst; Enzymatic reaction;86%
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 galactokinase from Bifidobacterium infantis; inorganic pyrophosphatase from P. multocida; UDP-sugar pyrophosphorylase from Arabidopsis thaliana; ATP; sodium hydroxide; magnesium chloride In aq. buffer at 37℃; for 24h; pH=7.5; Enzymatic reaction;
ammonium 2-acetamido-2,6-dideoxy-α-D-glucopyranosyl-1-phosphate

ammonium 2-acetamido-2,6-dideoxy-α-D-glucopyranosyl-1-phosphate

uridine 5'-diphospho-2-acetamido-2,6-dideoxy-α-D-glucopyranose diammonium salt

uridine 5'-diphospho-2-acetamido-2,6-dideoxy-α-D-glucopyranose diammonium salt

Conditions
ConditionsYield
With pyrophosphatase from C. cerevisiae; uridyl transferase GlmU from E. coli K12; magnesium chloride In aq. buffer at 37℃; for 24h; pH=7.5; Enzymatic reaction;86%
C8H14NO9P(2-)*2Na(1+)

C8H14NO9P(2-)*2Na(1+)

P'-[2-(acetylamino)-2-deoxy-α-D-glucopyranosyl] ester uridine 5'-(trihydrogen diphosphate), disodium salt
91183-98-1

P'-[2-(acetylamino)-2-deoxy-α-D-glucopyranosyl] ester uridine 5'-(trihydrogen diphosphate), disodium salt

Conditions
ConditionsYield
With 1,4-dithio-D,L-threitol; magnesium chloride at 30℃; for 3h; pH=7; aq. buffer; Enzymatic reaction;85%
ammonium 2-acetamido-6-azido-2,6-dideoxy-α-D-glucopyranosyl-1-phosphate

ammonium 2-acetamido-6-azido-2,6-dideoxy-α-D-glucopyranosyl-1-phosphate

uridine 5'-diphospho-2-acetamido-6-azido-2,6-dideoxy-α-D-glucopyranose diammonium salt

uridine 5'-diphospho-2-acetamido-6-azido-2,6-dideoxy-α-D-glucopyranose diammonium salt

Conditions
ConditionsYield
With pyrophosphatase from C. cerevisiae; uridyl transferase GlmU from E. coli K12; magnesium chloride In aq. buffer at 37℃; for 48h; pH=7.5; Enzymatic reaction;84%
Conditions
ConditionsYield
With Pasteurella multocida inorganic pyrophosphatase; Pasteurella multocida N-acetylglucosamine-1-phosphate uridylyltransferase; adenosine-5'-triphosphate; MTESNEVLFGIASHFALEGAVTGIEPYGDGHINTTYLVTTDGPRYILQQMNTSIFPDTVNLMRNVELVTSTLKAQGKETLDIVPTTSGATWAEIDGGAWRVYKFIEHTMSYNLVPNPDVFREAGSAFGDFQNFLSEFDASQLTETIAHFHDTPHRFEDFKAALAADKLGRAAACCPEIDFYLSHADQYAVVMDGLRDGSIPLRVTHNDTKLNNILMDATTGKARAIIDLDTIMPGSMLFDFGDSIRFGASTALEDERDLSKVHFSTELFRAYTEGFVGELRGSITAREAELLPFSGNLLTMECGMRFLADYLEGDIYFATKYPEHNLVRTRTQIKLVQEMEQKASETHAIVADIMEAARLE; magnesium chloride In water at 37℃; for 24h; pH=8; Enzymatic reaction;83%
With recombinant human GalNAc kinase GK2; recombinant human UDP-GalNAc pyrophosphorylase AGX1; ATP; yeast inorganic pyrophosphatase In various solvent(s) at 37℃; for 6h; pH=8.8;68%
With pyrophosphatase; N-acetylhexosamine kinase; GalNAc pyrophosphorylase; ATP In aq. buffer at 37℃; pH=7.5; Enzymatic reaction;
With Bifidobacterium longum subsp. longum N-acetylhexosamine 1-kinase; Escherichia coli N-acetylglucosamine 1-phosphate uridyltransferase; ATP; sodium hydroxide; magnesium chloride In aq. buffer at 37℃; for 7h; pH=8.5; Inert atmosphere; Enzymatic reaction;
Conditions
ConditionsYield
With inorganic pyrophosphatase cloned from Pasteurella multocida strain P-1059; N-acetylglucosamine-1-phosphate uridylyltransferase cloned from Pasteurella multocida strain P-1059 (ATCC15742); N-acetylhexosamine 1-kinase cloned from Bifidobacterium longum ATCC55813; ATP; magnesium chloride In water at 37℃; pH=8; aq. buffer; Enzymatic reaction;81%
With Pasteurella multocida inorganic pyrophosphatase; Pasteurella multocida N-acetylglucosamine-1-phosphate uridylyltransferase; adenosine-5'-triphosphate; MTESNEVLFGIASHFALEGAVTGIEPYGDGHINTTYLVTTDGPRYILQQMNTSIFPDTVNLMRNVELVTSTLKAQGKETLDIVPTTSGATWAEIDGGAWRVYKFIEHTMSYNLVPNPDVFREAGSAFGDFQNFLSEFDASQLTETIAHFHDTPHRFEDFKAALAADKLGRAAACCPEIDFYLSHADQYAVVMDGLRDGSIPLRVTHNDTKLNNILMDATTGKARAIIDLDTIMPGSMLFDFGDSIRFGASTALEDERDLSKVHFSTELFRAYTEGFVGELRGSITAREAELLPFSGNLLTMECGMRFLADYLEGDIYFATKYPEHNLVRTRTQIKLVQEMEQKASETHAIVADIMEAARLE; magnesium chloride In aq. buffer at 37℃; Enzymatic reaction;81%
With inorganic pyrophosphatase; glucose-1-phosphate thymidylyltransferase from Aneurinibacillus thermoaerophilus DSM10155; N-acetylhexosamine kinase from Bifidobacterium longum; ATP; magnesium chloride In aq. buffer at 37 - 55℃; for 4h; pH=7.5; Enzymatic reaction;
With hydrogenchloride; N-acetylglucosamine-1-phosphate uridylyltransferase from Escherichia coli K12 MG1655; pyrophosphatase from Escherichia coli K12 MG1655; recombinant N-acetylhexosamine 1-kinase; ATP; magnesium chloride In aq. buffer at 37℃; pH=8.5; Concentration; Temperature; pH-value; Enzymatic reaction;
With inorganic pyrophosphatase from P. multocida; N-acetyl hexosamine 1-kinase from Bifidobacterium infantis; UDP-N-acetylgalactosamine pyrophosphorylase from Pasteurella multocida; ATP; sodium hydroxide; magnesium chloride In aq. buffer at 37℃; for 24h; pH=7.5; Enzymatic reaction;
Conditions
ConditionsYield
With N-iodo-succinimide; sodium azide In water for 15h; regioselective reaction;80%
With N-iodo-succinimide; sodium azide In water at 60℃; for 15h; regioselective reaction;79%
Conditions
ConditionsYield
With recombinant Arabidopsis thaliana glucuronokinase; molecular weight around 42 kDa; recombinant Bifidobacterium longum UDP-sugar pyrophosphorylase; recombinant Pasteurella multocida inorganic pyrophosphatase; ATP; magnesium chloride In aq. buffer at 37℃; for 36h; pH=6.5; Catalytic behavior; Reagent/catalyst; pH-value; Enzymatic reaction; chemoselective reaction;80%
With glucuronokinase from Arabidopsis thaliana; inorganic pyrophosphatase from P. multocida; UDP-sugar pyrophosphorylase from Arabidopsis thaliana; ATP; sodium hydroxide; magnesium chloride In aq. buffer at 37℃; for 24h; pH=7.5; Enzymatic reaction;
2-deoxy-2-propionylamido-α-D-glucopyranosyl phosphate

2-deoxy-2-propionylamido-α-D-glucopyranosyl phosphate

uridine-5'-(2-deoxy-2-propionylamido-α-D-glucopyranosyl diphosphate)

uridine-5'-(2-deoxy-2-propionylamido-α-D-glucopyranosyl diphosphate)

Conditions
ConditionsYield
With yeast inorganic pyrophosphatase; N-acetylglucosamine-1-phosphate pyrophosphorylase from C. jejuni NCTC 11168; tris hydrochloride; magnesium chloride at 37℃; for 2h; pH=7.5;79.9%
Conditions
ConditionsYield
With Glucose-1-phosphate thymidylyltransferase from Streptococcus pneumonia serotype 23F for 48h; Enzymatic reaction;78%
With phosphate buffer; UDPG-PPase from Pyrococcus furiosus DSM 3638 at 90℃; pH=7.5; Enzyme kinetics;
With phosphate buffer; UDPG-PPase from Pyrococcus furiosus DSM 3638; magnesium chloride at 90℃; for 0.5h;92 % Turnov.
Conditions
ConditionsYield
With galactokinase; pyruvate kinase; inorganic pyrophosphatase; phosphoenolpyruvic acid; galactose-1-phosphate uridylyltransferase; GalU; ATP; uridine-5'-diphosphoglucose at 30℃; for 24h; pH=8; aq. phosphate buffer; Inert atmosphere;78%
With inorganic pyrophosphatase; galactokinase from Meiothermus taiwanensis; UDP-sugar pyrophosphorylase pyrophosphorylase from Arabidopsis thaliana; ATP; magnesium chloride In aq. buffer at 42℃; for 1h; pH=9; Enzymatic reaction;
2-Deoxy-2-[(trifluoroacetyl)amino]-D-glucopyranose-1-(dihydrogen phosphate) disodium salt

2-Deoxy-2-[(trifluoroacetyl)amino]-D-glucopyranose-1-(dihydrogen phosphate) disodium salt

P'-[2-deoxy-2-[(2,2,2-trifluoroacetyl)amino]-α-D-glucopyranosyl] ester uridine 5'-(trihydrogen diphosphate), disodium salt

P'-[2-deoxy-2-[(2,2,2-trifluoroacetyl)amino]-α-D-glucopyranosyl] ester uridine 5'-(trihydrogen diphosphate), disodium salt

Conditions
ConditionsYield
With 1,4-dithio-D,L-threitol; magnesium chloride at 30℃; for 3h; pH=7; aq. buffer; Enzymatic reaction;78%
adenosine 5'-phosphorimidazolide
20816-58-4, 116273-87-1

adenosine 5'-phosphorimidazolide

P1-5'-O-adenosine-P4-5'-O-uridine tetraphosphate

P1-5'-O-adenosine-P4-5'-O-uridine tetraphosphate

Conditions
ConditionsYield
With H96F-Fhit; magnesium chloride In various solvent(s) at 20℃; for 1h; pH=5.5;73%
2-acetamido-6-azido-2,6-dideoxy-D-glucopyranoside

2-acetamido-6-azido-2,6-dideoxy-D-glucopyranoside

uridine 5'-diphospho-2-acetamido-6-azido-2,6-dideoxy-α-D-glucopyranoside
1202854-85-0

uridine 5'-diphospho-2-acetamido-6-azido-2,6-dideoxy-α-D-glucopyranoside

Conditions
ConditionsYield
With inorganic pyrophosphatase cloned from Pasteurella multocida strain P-1059; N-acetylglucosamine-1-phosphate uridylyltransferase cloned from Pasteurella multocida strain P-1059 (ATCC15742); N-acetylhexosamine 1-kinase cloned from Bifidobacterium longum ATCC55813; ATP; magnesium chloride In water at 37℃; pH=8; aq. buffer; Enzymatic reaction;72%
UDP-glucose
133-89-1

UDP-glucose

C6H13O8P
1375486-69-3

C6H13O8P

uridine-5'-diphospho-5-deoxy-D-galactofuranose
1346254-09-8

uridine-5'-diphospho-5-deoxy-D-galactofuranose

Conditions
ConditionsYield
With inorganic pyrophosphatase; UDP-glucose pyrophosphorylase; galactose-1-phosphate uridyltransferase71%
2-butyramido-2-deoxy-α-D-glucopyranosyl phosphate
884856-17-1

2-butyramido-2-deoxy-α-D-glucopyranosyl phosphate

uridine-5'-(2-butyramido-2-deoxy-α-D-glucopyranosyl diphosphate)

uridine-5'-(2-butyramido-2-deoxy-α-D-glucopyranosyl diphosphate)

Conditions
ConditionsYield
With yeast inorganic pyrophosphatase; N-acetylglucosamine-1-phosphate pyrophosphorylase from C. jejuni NCTC 11168; tris hydrochloride; magnesium chloride at 37℃; for 2h; pH=7.5;70.6%
UDP-glucose
133-89-1

UDP-glucose

6-deoxy-α-D-galactofuranosyl phosphate

6-deoxy-α-D-galactofuranosyl phosphate

uridine-5'-diphospho-6-deoxy-D-galactofuranose
1000874-38-3

uridine-5'-diphospho-6-deoxy-D-galactofuranose

Conditions
ConditionsYield
With inorganic pyrophosphatase; UDP-glucose pyrophosphorylase; galactose-1-phosphate uridyltransferase70%
C8H14NO9P(2-)*2Na(1+)

C8H14NO9P(2-)*2Na(1+)

P'-[2-(acetylamino)-2-deoxy-α-D-galactopyranosyl] ester uridine 5'-(trihydrogen diphosphate), disodium salt
108320-87-2

P'-[2-(acetylamino)-2-deoxy-α-D-galactopyranosyl] ester uridine 5'-(trihydrogen diphosphate), disodium salt

Conditions
ConditionsYield
With 1,4-dithio-D,L-threitol; magnesium chloride at 30℃; for 48h; pH=7; aq. buffer; Enzymatic reaction;70%

Uridine 5'-(tetrahydrogen triphosphate) Chemical Properties

IUPAC  Name: [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-Dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate       
Empirical Formula: C9H15N2O15P3
Molecular Weight: 484.1411 
Classification Code : Mutation data
Einecs: 200-558-7
Freely Rotating Bonds: 10
Polar Surface Area: 213.56 Å2
Index of Refraction: 1.643
Molar Refractivity: 83.19 cm3
Molar Volume: 229.8 cm3
Polarizability: 32.98 ×10-24 cm3
Surface Tension: 128.1 dyne/cm
Density: 2.106 g/cm3
The molecular structure of  Uridine5'-(tetrahydrogen triphosphate) (CAS NO.63-39-8) is
.

Uridine 5'-(tetrahydrogen triphosphate) Uses

  Uridine5'-(tetrahydrogen triphosphate) (CAS NO.63-39-8) is used as organic intermediate.

Uridine 5'-(tetrahydrogen triphosphate) Safety Profile

Hazard Codes: HarmfulXn
Risk Statements: 20/21/22-68-20/21/22 
R20/21/22: Harmful by inhalation, in contact with skin and if swallowed. 
R68: Possible risk of irreversible effects.
Safety Statements: 22-26-36 
S22: Do not breathe dust. 
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. 
S36: Wear suitable protective clothing.
WGK Germany: 1

Uridine 5'-(tetrahydrogen triphosphate) Specification

The chemical synonyms of  Uridine5'-(tetrahydrogen triphosphate) (CAS NO.63-39-8) are Uridine 5'-triphosphate ;Uridine 5'-triphosphoric acid ;Uridine triphosphate ;Uteplex .

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