CAS 25110-76-3

5-ethyluridine

Description:

5-Ethyluridine is a nucleoside analog derived from uridine, characterized by the presence of an ethyl group at the 5-position of the pyrimidine ring. This modification can influence its biological activity and interactions with nucleic acid structures. The molecular formula of 5-ethyluridine reflects its composition of carbon, hydrogen, nitrogen, and oxygen atoms, typical of nucleosides. It is soluble in water and exhibits properties that allow it to participate in various biochemical processes, including potential roles in RNA synthesis and metabolism. The compound is of interest in research, particularly in the fields of molecular biology and medicinal chemistry, where it may serve as a tool for studying RNA function or as a potential therapeutic agent. Its CAS number, 25110-76-3, is a unique identifier that facilitates the tracking and referencing of this specific chemical substance in scientific literature and databases. Overall, 5-ethyluridine exemplifies the structural diversity of nucleosides and their importance in biological systems.

Formula: C₁₁H₁₆N₂O₆

InChI: InChI=1/C11H16N2O6/c1-2-5-3-13(11(18)12-9(5)17)10-8(16)7(15)6(4-14)19-10/h3,6-8,10,14-16H,2,4H2,1H3,(H,12,17,18)/t6-,7-,8-,10-/m1/s1

SMILES: CCc1cn([C@H]2[C@@H]([C@@H]([C@@H](CO)O2)O)O)c(=O)nc1O

Synonyms:

• Uridine, 5-ethyl-

Uridine, 5-ethyl-

CAS: 25110-76-3

Formula: C₁₁H₁₆N₂O₆

Purity: 97%

Color and Shape: Solid

Molecular weight: 272.2545

Ref: IN-DA002QIL

1-((2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-ethylpyrimidine-2,4(1H,3H)-dione

CAS: 25110-76-3

1-((2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-ethylpyrimidine-2,4(1H,3H)-dione

Purity: 97%

Molecular weight: 272.26g/mol

Ref: 54-OR1069085

5-Ethyluridine

CAS: 25110-76-3

5-Ethyluridine is a 5-Modified Pyrimidine Nucleoside.

Formula: C₁₁H₁₆N₂O₆

Color and Shape: Solid

Molecular weight: 272.25

Ref: TM-TNU0122

5-Ethyluridine

CAS: 25110-76-3

5-Ethyluridine is a modified form of uridine. The ethyl group on the 5-position of uridine has been replaced by an ethyl group. This modification inhibits the growth of bacteria, which may be due to inhibition of purine synthesis or due to conformational changes in the active site. It is not clear why this modification inhibits bacterial growth, but it does not inhibit human cell growth.

Purity: Min. 95%

Ref: 3D-FE144818