Merck
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U3750

Sigma-Aldrich

Uridine

≥99%

Synonym(s):
1-β-D-Ribofuranosyluracil, Uracil-1-β-D-ribofuranoside
Empirical Formula (Hill Notation):
C9H12N2O6
CAS Number:
Molecular Weight:
244.20
Beilstein:
754902
Numer EC:
Numer MDL:
Identyfikator substancji w PubChem:
NACRES:
NA.51

pochodzenie biologiczne

synthetic (organic)

Poziom jakości

200

próba

≥99%

forma

powder

mp

163-167 °C (lit.)

rozpuszczalność

H2O: 50 mg/mL, clear, colorless

SMILES string

OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N2C=CC(=O)NC2=O

InChI

1S/C9H12N2O6/c12-3-4-6(14)7(15)8(17-4)11-2-1-5(13)10-9(11)16/h1-2,4,6-8,12,14-15H,3H2,(H,10,13,16)/t4-,6-,7-,8-/m1/s1

InChI key

DRTQHJPVMGBUCF-XVFCMESISA-N

Gene Information

mouse ... Uck1(22245)

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Opis ogólny

Uridine is a uracil nucleoside, specific for RNA sequence. Uridine is present in blood, seminal fluid and cerebrospinal fluid. Uridine is synthesized in living organisms by de novo and salvage pathways.

Zastosowanie

Uridine has been used:
  • as a component of hippocampal neuron medium for culture of primary hippocampal neuron cells
  • in uridine rescue experiments in mouse embryonic fibroblasts and human breast cancer cells
  • in chase sequencing experiments

Opakowanie

1, 25, 100 g in poly bottle

Działania biochem./fizjol.

Uridine monophosphate is essential for protein glycosylation, polysaccharide biosynthesis and lipid metabolism. Oral administration of uridine is suggested for anisopoikilocytosis and epileptic encephalopathy disorders. Uridine has numerous biological functions like treating dry eye syndrome, regulating nervous system and favors reproduction. High levels of uridine are implicated in insulin resistance.

Kod klasy składowania

11 - Combustible Solids

WGK

WGK 3

Temperatura zapłonu °F

Not applicable

Temperatura zapłonu °C

Not applicable

Środki ochrony indywidualnej

Eyeshields, Gloves, type N95 (US)

Certificate of Analysis

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Certificate of Origin

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