A
disodium uridine-5'-monophosphate
B
5-dimethylamino-1-hydroxymethylisoquinoline
Conditions | Yield |
---|---|
With snake venom phosphodiesterase for 3h; enzymatic hydrolysis; var.: pH; |
A
disodium uridine-5'-monophosphate
B
5-dimethylamino-1-hydroxymethylisoquinolin-2-oxide
Conditions | Yield |
---|---|
With sodium acetate; snake venom phosphodiesterase at 37℃; for 3h; enzymatic hydrolysis, pH=8; half-life=7 h (pH=4.1), 12 h (pH=10.1), 24 h (pH=7.1), T=37 deg C; |
orotic acid sodium salt
5-phospho-D-ribosyl α-1-pyrophosphate
disodium uridine-5'-monophosphate
Conditions | Yield |
---|---|
With DL-dithiothreitol; magnesium chloride for 192h; PAN-immobilized O-5-decarboxylase, O-5-P-pyrophosphorylase, PPiase; Yield given; |
Conditions | Yield |
---|---|
Multistep reaction.; |
disodium uridine-5'-monophosphate
Conditions | Yield |
---|---|
With ODCase from Methanobacterium thermoautotrophicum In various solvent(s) at 55℃; pH=7.5; Enzyme kinetics; Further Variations:; Temperatures; | |
With orotidine 5'-monophosphate decarboxylase mutant Q215A/Y217F/R235A In aq. buffer at 25℃; pH=7.1; Kinetics; Reagent/catalyst; Enzymatic reaction; |
D-Ribose
disodium uridine-5'-monophosphate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: Na2ATP, MgCl2*6H2O, PEP-K+, DTT, K2HPO4, Na2EDTA / 72 h / PAN-immobilized pyruvate kinase, adenylate kinase, PRPP synthetase, pH 7.5 2: MgCl2*6H2O, DTT / 192 h / PAN-immobilized O-5-decarboxylase, O-5-P-pyrophosphorylase, PPiase View Scheme |
α,β-D-ribofuranose-5-phophate disodium salt
disodium uridine-5'-monophosphate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 70 mmol / Na2ATP, MgCl2*6H2O, PEP-K+, K2HPOu, Na2EDTA / 96 h / 30 °C / immobilized PRPP synthetase, pyruvate kinase, adenylate kinase, pH 7.4 2: MgCl2*6H2O, DTT / 192 h / PAN-immobilized O-5-decarboxylase, O-5-P-pyrophosphorylase, PPiase View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 94 percent / Dowex 50 W-X8 (H+ form) / H2O / 0.14 h / Heating 2: 70 mmol / Na2ATP, MgCl2*6H2O, PEP-K+, K2HPOu, Na2EDTA / 96 h / 30 °C / immobilized PRPP synthetase, pyruvate kinase, adenylate kinase, pH 7.4 3: MgCl2*6H2O, DTT / 192 h / PAN-immobilized O-5-decarboxylase, O-5-P-pyrophosphorylase, PPiase View Scheme |
disodium uridine-5'-monophosphate
Conditions | Yield |
---|---|
With water; zinc(II) cation pH=5.5; |
Conditions | Yield |
---|---|
Stage #1: disodium uridine-5'-monophosphate With DOWEX IR100S resin In water Industrial scale; Stage #2: tributyl-amine In water at 15 - 25℃; pH=6.5 - 7.5; Industrial scale; | 91.4% |
With DOWEX IR100S resin In water at 15 - 25℃; pH=6.5 - 7.5; Industrial scale; | 91.4% |
With DOWEX 50WX2-200 (H) |
disodium uridine-5'-monophosphate
acetic anhydride
tributylammonium 2',3'-di-O-acetyluridine 5'-monophosphate
Conditions | Yield |
---|---|
In pyridine; N,N-dimethyl-formamide | 72% |
Conditions | Yield |
---|---|
In ethanol for 0.5h; | 68% |
disodium uridine-5'-monophosphate
thioacetic acid
2′,3′-di-O-acetyl β-uridine-5′-phosphate
Conditions | Yield |
---|---|
With propiolonitrile; sodium hydroxide In water; water-d2 pH=8; | 67% |
disodium uridine-5'-monophosphate
water
trans-1,2-bis(4-pyridyl)ethylene
Conditions | Yield |
---|---|
In ethanol for 0.5h; | 63% |
disodium uridine-5'-monophosphate
A
1,3-dimethyl-2-imidazolidinone
B
Up2U
Conditions | Yield |
---|---|
at 37℃; for 24h; | A 40% B n/a |
α-2-azido-2-deoxy-3,4,6-tri-O-acetyl-D-galactose 1-phosphate
disodium uridine-5'-monophosphate
Conditions | Yield |
---|---|
Stage #1: disodium uridine-5'-monophosphate In water for 0.5h; Stage #2: With tributyl-amine In water at 20℃; for 0.5h; Stage #3: α-2-azido-2-deoxy-3,4,6-tri-O-acetyl-D-galactose-1-phosphate Further stages; | 37% |
disodium uridine-5'-monophosphate
methyl iodide
A
3'-O-methyluridine 5'-monophosphate
B
2',3'-di-O-methyluridine 5'-monophosphate
C
2'-O-methyluridine 5'-monophosphate monosodium salt
Conditions | Yield |
---|---|
With sodium hydroxide In 1,4-dioxane for 3h; Ambient temperature; various alkyl iodides, other temperature; | A 11% B 33% C 20% |
With sodium hydroxide In 1,4-dioxane for 3h; Ambient temperature; | A 11% B 33% C 20% |
Conditions | Yield |
---|---|
In water uridine 5'-monophosphate disodium salt (0.076 mmol) added to aq. soln. of Cu complex (0.059 mmol); stirred (12 h); concd. (vac.); concd. slowly; crystals collected; dried (vac.); elem. anal.; | 30% |
disodium uridine-5'-monophosphate
Conditions | Yield |
---|---|
Stage #1: disodium uridine-5'-monophosphate With 1H-imidazole; 2-chloro-1,3-dimethylimidazolinium chloride In water-d2 at 37℃; for 1h; Inert atmosphere; Stage #2: 2-azido-2-deoxy-α-D-galactofuranosyl phosphate triethylammonium salt In water-d2 at 37℃; for 18h; Inert atmosphere; Stage #3: With calf intestinal alkaline phosphatase In water-d2 at 30℃; for 24h; pH=8; Inert atmosphere; Enzymatic reaction; | 23% |
disodium uridine-5'-monophosphate
ethyl iodide
A
3'-O-ethyluridine 5'-monophosphate
B
2'-O-ethyluridine 5'-monophosphate
C
2',3'-di-O-ethyluridine 5'-monophosphate disodium salt
Conditions | Yield |
---|---|
With sodium hydroxide In 1,4-dioxane at 65℃; for 3h; | A 22% B 18% C 18% |
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% |
disodium uridine-5'-monophosphate
Conditions | Yield |
---|---|
Stage #1: disodium uridine-5'-monophosphate With 1H-imidazole; 2-chloro-1,3-dimethylimidazolinium chloride In water-d2 at 37℃; for 1h; pH=8; Inert atmosphere; Stage #2: 2-acetamido-2-deoxy-α-D-galactofuranosyl phosphate triethylammonium salt In water-d2 at 37℃; for 24h; Inert atmosphere; Stage #3: With calf intestinal alkaline phosphatase In water-d2 at 30℃; for 24h; pH=8; Inert atmosphere; Enzymatic reaction; | 16% |
disodium uridine-5'-monophosphate
1-iodo-propane
A
2'-O-n-propyluridine 5'-monophosphate
B
2',3'-di-O-n-propyluridine 5'-monophosphate monosodium salt
Conditions | Yield |
---|---|
With sodium hydroxide In 1,4-dioxane at 70℃; for 3h; | A 13% B 13% |
2-iodo-propane
disodium uridine-5'-monophosphate
A
3'-O-isopropyluridine 5'-monophosphate monosodium salt
B
uridine 5'-monophosphate isopropyl ester monosodium salt
Conditions | Yield |
---|---|
With sodium hydroxide In 1,4-dioxane at 70℃; for 3h; | A 9% B 10% |
1-nitro-3-vinyl-benzene
disodium uridine-5'-monophosphate
5(E)-(3-nitrostyryl)uridine 5'-phosphate
Conditions | Yield |
---|---|
With lithium pentachloropalladate; mercury(II) diacetate 1) water, 50 deg C, 5 h; 2) methanol, 30 min; Yield given. Multistep reaction; |
disodium uridine-5'-monophosphate
[(1S)-2-imidazol-1-yl-1-methyl-2-oxo-ethyl]-carbamic acid tert-butyl ester
Conditions | Yield |
---|---|
In water at 20 - 22℃; for 2.5h; various nucleoside 5'-phosphates, syntheses of 2'(3')-O-aminoacylnucleosides; |
disodium uridine-5'-monophosphate
5-dimethylamino-2-oxidoisoquinolin-1-yl diazomethane
Conditions | Yield |
---|---|
In water for 0.333333h; Ambient temperature; pH=5 (HCl); |
Conditions | Yield |
---|---|
With pyridine In N,N-dimethyl-formamide for 24h; Ambient temperature; |
disodium uridine-5'-monophosphate
chlorophosphoric acid diphenyl ester
uridine 5'-(diphenyl diphosphate)
Conditions | Yield |
---|---|
With tributyl-amine In 1,4-dioxane; N,N-dimethyl-formamide |
disodium uridine-5'-monophosphate
Conditions | Yield |
---|---|
With 1,1'-carbonyldiimidazole 1.) acetone, 18 h, room temp., 2.) DMF, 18 h, room temp.; Multistep reaction; |
disodium uridine-5'-monophosphate
Conditions | Yield |
---|---|
With triethylamine In acetonitrile at 0℃; for 3h; |
disodium uridine-5'-monophosphate
pyrenyl-1-diazomethane
Conditions | Yield |
---|---|
With boric acid In ethyl acetate; acetonitrile at 60℃; |
1-methyl-1H-imidazole
disodium uridine-5'-monophosphate
trifluoroacetic anhydride
Conditions | Yield |
---|---|
Stage #1: disodium uridine-5'-monophosphate; trifluoroacetic anhydride With triethylamine In acetonitrile at 0 - 20℃; Stage #2: 1-methyl-1H-imidazole With triethylamine In acetonitrile at 0℃; for 0.166667h; |
Uridine 5'-Monophosphate Disodium Salt Hydrate, with the CAS NO.3387-36-8, is also called Disodium [(2R,3S,4S,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate; 5'-UMP disodium; CCRIS 6562; Disodium 5'-UMP; Disodium 5'-uridylate; Disodium UMP ; Disodium uridine 5'-monophosphate; Disodium uridine 5'-phosphate; EINECS 222-211-9 ; NSC 20257; Uridine 5'MP, disodium salt; Uridine-5-monophosphate disodium salt. It belongs to Biochemistry; Nucleosides, Nucleotides & Related Reagents; Nucleotides and their analogs; Nucleic acids. Uridine 5'-Monophosphate Disodium Salt Hydrate is used as flavoring agent.
Physical properties about Uridine 5'-Monophosphate Disodium Salt Hydrate are: (1)ACD/LogP: -1.583; (2)# of Rule of 5 Violations: 2; (3)ACD/LogD (pH 5.5): -4.92; (4)ACD/LogD (pH 7.4): -5.90; (5)ACD/BCF (pH 5.5): 1.00; (6)ACD/BCF (pH 7.4): 1.00; (7)ACD/KOC (pH 5.5): 1.00; (8)ACD/KOC (pH 7.4):1.00; (9)#H bond acceptors: 11; (10)#H bond donors: 5; (11)#Freely Rotating Bonds: 6
Uses of Uridine 5'-Monophosphate Disodium Salt Hydrate: Uridine 5'-Monophosphate Disodium Salt Hydrate is used as flavoring agent: nucleotide added to the milk to increase volume to make it closer to human milk composition, increase resistance to infants and young children. And it can be used as auxiliary liver disease drug. It also used as production of intermediate nucleic acid drugs asn health food and biochemical reagents. And it for the manufacture of uridine triphosphate (UTP), poly gland urine, drugs such Furtulon.
When you are using this chemical, please be cautious about it as the following:
1. Do not breathe dust;
2. Avoid contact with skin and eyes;
3. Wear suitable protective clothing;
4. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice;
You can still convert the following datas into molecular structure:
(1)InChI=1S/C9H13N2O9P.2Na/c12-5-1-2-11(9(15)10-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18;;/h1-2,4,6-8,13-14H,3H2,(H,10,12,15)(H2,16,17,18);;/q;2*+1/p-2/t4-,6-,7+,8-;;/m1../s1;
(2)InChIKey=KURVIXMFFSNONZ-WAJQJQIOSA-L;
(3)Smilesc1cn(c(=O)[nH]c1=O)[C@H]2[C@H]([C@@H]([C@H](O2)COP(=O)([O-])[O-])O)O.[Na+].[Na+]
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | intraperitoneal | 3394mg/kg (3394mg/kg) | LUNGS, THORAX, OR RESPIRATION: CYANOSIS BEHAVIORAL: ATAXIA BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) | Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 22, Pg. 618, 1975. |
mouse | LD50 | oral | > 12gm/kg (12000mg/kg) | LUNGS, THORAX, OR RESPIRATION: DYSPNEA BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) | Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 22, Pg. 618, 1975. |
mouse | LD50 | subcutaneous | 3698mg/kg (3698mg/kg) | BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) | Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 22, Pg. 618, 1975. |
rat | LD50 | intraperitoneal | 3111mg/kg (3111mg/kg) | LUNGS, THORAX, OR RESPIRATION: CYANOSIS BEHAVIORAL: ATAXIA BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) | Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 22, Pg. 618, 1975. |
rat | LD50 | oral | > 12gm/kg (12000mg/kg) | Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 22, Pg. 618, 1975. | |
rat | LD50 | subcutaneous | > 6gm/kg (6000mg/kg) | BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) SKIN AND APPENDAGES (SKIN): "DERMATITIS, IRRITATIVE: AFTER SYSTEMIC EXPOSURE" | Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 22, Pg. 618, 1975. |
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