58-97-9
- Product Name：UMP
- Molecular Formula：C9H13 N2 O9 P
- Purity：99%
- Molecular Weight：324.184
Product Details
Veterinary Grade Feed Additives 5'-Uridylic acid(UMP) 58-97-9
- Molecular Formula:C9H13 N2 O9 P
- Molecular Weight:324.184
- Melting Point:202°C (rough estimate)
- Boiling Point:°Cat760mmHg
- PKA:pK1:6.63 (25°C)
- Flash Point:°C
- PSA：181.12000
- Density:1.865 g/cm3
- LogP:-2.73490
Feed Additives 5'-Uridylic acid(UMP) 58-97-9 Usage
5'-Uridylic acid(UMP) a nucleotide that is synthesized from uridine. It is used in foods such as infant formula to as a method of increasing uridine levels in blood. UMP had an important impact on the levels of metabolites and endocrine hormones in pre-weaning and young goats.
InChI:InChI=1/C9H13N2O9P/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)/t4-,6-,7-,8-/m1/s1
58-97-9 Relevant articles
Effects of 5′-uridylic acid feeding on postprandial plasma concentrations of GH, insulin and metabolites in young calves
K Katoh, K Yoshioka, H Hayashi, T Mashiko1 , M Yoshida, Y Kobayashi and Y Obara
Journal of Endocrinology (2005) 186, 157–163
Postprandial changes in plasma concentrations of GH, insulin, IGF-I, leptin and metabolites were compared between young Holstein bull calves fed with milk alone (control group) and with milk+5-uridylic acid (UMP) (UMP group). UMP (2 g/day) was given with milk at 0830 h and 1530 h for 11 days from the 4th to the 14th day after birth.
Significance of the enzyme complex that synthesizes UMP in ehrlich ascites cells
Thomas W. Traut
Archives of Biochemistry and Biophysics Volume 200, Issue 2, 1 April 1980, Pages 590-594
The de novo biosynthesis of pyrimidine nucleotides is completed by two sequential enzyme activities that convert orotate plus 5-phosphoribosyl-1-pyrophosphate to orotidine-5′-monophosphate (OMP) and PPi and then decarboxylate OMP to produce 5′-uridylic acid.
58-97-9 Process route
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yeast RNA
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yeast RNA
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- 63-37-6,30811-80-4
cytidine monophosphate
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- 58-97-9,27416-86-0
5'-Uridylic Acid
-
- 61-19-8,24937-83-5,67583-85-1
5'-adenosine monophosphate
-
- 85-32-5
Guanosine 5'-monophosphate
| Conditions | Yield |
|---|---|
|
With barley roots 5'-phosphodiesterase; at 70 ℃; for 0.5h; pH=5; aq. acetate buffer; Enzymatic reaction;
|
-
-
A(2'p5'A)3'p5'U
-
- 58-97-9,27416-86-0
5'-Uridylic Acid
-
- 61-19-8,24937-83-5,67583-85-1
5'-adenosine monophosphate
| Conditions | Yield |
|---|---|
|
With SVP (1 unit); In water; at 37 ℃; for 12h; Product distribution; HPLC analysis; no reaction with RNaseT2 or spleen phosphodiesterase;
|
58-97-9 Upstream products
-
362-43-6
2',3'-O-isopropylideneuridine
-
65-86-1
orotic acid
-
3257-71-4
(R)-2',3'-O-benzylideneuridine
-
97-55-2
5-phosphoribosyl-1-pyrophosphate
58-97-9 Downstream products
-
2149-79-3
5-Brom-uridin-5'-phosphat
-
4004-57-3
uridine 3',5'-cyclic monophosphate
-
58-98-0
UDP
-
63-39-8
UTP
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