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HomeProduct name listUridine 5′-monophosphate disodium salt

Uridine 5′-monophosphate disodium salt

Synonym(s):5′-UMP-Na2;U 5′-P;UMP;Uridine 5′-monophosphate disodium salt;Uridylic acid disodium salt

  • CAS NO.:3387-36-8
  • Empirical Formula: C9H14N2NaO9P
  • Molecular Weight: 348.18
  • MDL number: MFCD00006525
  • EINECS: 222-211-9
  • SAFETY DATA SHEET (SDS)
  • Update Date: 2024-11-21 15:02:05
Uridine 5′-monophosphate disodium salt  Structural

What is Uridine 5′-monophosphate disodium salt ?

Chemical properties

Crystalline

Chemical properties

The protonation of disodium uridine-5'-monophosphate (UMP) and cytidine 5' -monophosphate (a homolog of UMP) not only depend on the electrostatic forces but also strongly depend on the solute–solvent interactions of the different species in the mixtures. In the case of UMP, the correlation analysis of log10 K2 and log10 K1 (including β and π*) shows the polarity parameter has a major role (about 58 and 56 %, respectively) and the negative sign of π* and positive sign of β indicate that a decrease in the polarity of the media increases the protonation constants[1].

The Uses of Uridine 5′-monophosphate disodium salt

A nucleotide that is a major component of ribonucleic acid. It is found in dietary supplements as well as natural RNA rich foods and has been shown to increase cognitive function in animals.

The Uses of Uridine 5′-monophosphate disodium salt

Uridine 5’-Monophosphate Disodium Salt is a derivative of Uridine (U829910) which is a major ribonucleic acid.

The Uses of Uridine 5′-monophosphate disodium salt

Uridine 5′-monophosphate disodium salt has been used to study the effect of pyrimidine synthesis inhibitor, 5-azacytidine, on cholesterol and lipid metabolism. It has been used to study the effect of nucleotides on growth of specific intestinal bacteria.

What are the applications of Application

Uridine 5′-monophosphate disodium salt is a nucleotide that is a major component of ribonucleic acid

General Description

Uridine 5′-monophosphate is a pyrimidine mononucleotide. It is formed by decarboxylation of orotidine 5′-monophosphate. UMP is further converted to UTP (uridine 5′-triphosphate) using kinases.

References

[1] Soleimani, Farahnaz, and F. Gharib. "Protonation Constants of Uridine 5′-Monophosphate in Different Aqueous Solutions of Methanol." Journal of Solution Chemistry 43.4(2014):763-773.

Properties of Uridine 5′-monophosphate disodium salt

Melting point: 208-210 °C
refractive index  -14 ° (C=1, H2O)
storage temp.  2-8°C
solubility  Water (Slightly)
form  Crystalline Powder
pka 6.4, 9.5(at 25℃)
color  White
Water Solubility  40 g/100 mL (20 ºC)
BRN  3582885
Stability: Very Hygroscopic
InChI InChI=1/C9H13N2O9P.Na.H/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-;;/s3
CAS DataBase Reference 3387-36-8(CAS DataBase Reference)

Safety information for Uridine 5′-monophosphate disodium salt

Computed Descriptors for Uridine 5′-monophosphate disodium salt

InChIKey KURVIXMFFSNONZ-WFIJOQBCSA-L
SMILES O[C@@H]1[C@@H]([C@@H](COP(O)(O)=O)O[C@H]1N1C=CC(=O)NC1=O)O.[NaH] |&1:1,2,3,11,r|

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