Uridine 5'-monophosphate-13C9,15N2 (dilithium)

Uridine 5'-monophosphate-13C9,15N2 (5'- Uridylic acid-13C9,15N2) dilithium is 13C and 15N-labeled Uridine 5'-monophosphate (HY-101981) . Uridine 5'-monophosphate (5'-Uridylic acid) is an orally active mitochondrial ATP-dependent potassium channel activator that has a protective effect on the heart. Uridine 5'-monophosphate can promote the synthesis of CDP-choline and induce apoptosis in intestinal epithelial cells, which is beneficial for gut development and reduces diarrhea[1][2][3].

Product Specifications

CAS Number

[2483830-55-1]

Product Name Alternative

5'-Uridylic acid-13C9,15N2 (dilithium)

UNSPSC

12352005

Target

Apoptosis; Cholinesterase (ChE) ; Endogenous Metabolite; Isotope-Labeled Compounds; Potassium Channel

Type

Isotope-Labeled Compounds

Related Pathways

Apoptosis; Membrane Transporter/Ion Channel; Metabolic Enzyme/Protease; Neuronal Signaling; Others

Applications

Metabolism-protein/nucleotide metabolism

Field of Research

Metabolic Disease; Cardiovascular Disease

Assay Protocol

https://www.medchemexpress.com/uridine-5-monophosphate-13c9-15n2-dilithium.html

Solubility

10 mM in DMSO

Smiles

O=P(O[Li])(O[Li])O[13CH2][13C@H]1O[13C@@H]([15N]([13C]([15NH]2)=O)[13CH]=[13CH][13C]2=O)[13C@H](O)[13C@@H]1O

Molecular Formula

13C9H11Li2 15N2O9P

Molecular Weight

346.97

References & Citations

[1]Li G, et al. Uridine/UMP metabolism and their function on the gut in segregated early weaned piglets. Food Funct. 2019 Jul 17;10 (7) :4081-4089.|[2]Mehmet Cansev, et al. Oral uridine-5'-monophosphate (UMP) increases brain CDP-choline levels in gerbils. Brain Res. 2005 Oct 5;1058 (1-2) :101-8.|[3]Irina B Krylova, et al. The cardioprotective effect of uridine and uridine-5'-monophosphate: the role of the mitochondrial ATP-dependent potassium channel. Exp Gerontol. 2006 Jul;41 (7) :697-703.