5-Aminouridine is a nucleoside analog characterized by the presence of an amino group at the 5-position of the uridine structure. It is a pyrimidine nucleoside, which consists of a ribose sugar linked to a uracil base. This compound is notable for its potential biological activity, particularly in antiviral and anticancer research, as it can interfere with nucleic acid synthesis. The amino group enhances its ability to form hydrogen bonds, which may influence its interaction with enzymes and other biomolecules. 5-Aminouridine is soluble in water, making it suitable for various biochemical applications. Its structural modifications compared to standard uridine may lead to altered pharmacokinetics and pharmacodynamics, making it a subject of interest in medicinal chemistry. Additionally, its CAS number, 2149-76-0, allows for precise identification in chemical databases and literature. Overall, 5-aminouridine serves as a valuable compound in the study of nucleoside analogs and their therapeutic potential.

5-aminouridine

2149-76-0: 5-amino-1-pentofuranosylpyrimidine-2,4(1H,3H)-dione

5-Aminouridine (4-Chloro-2-isopropyl-5-methylphenol(chlorothymol)) modifies nucleobases and is incorporated into the target DNA.

5-Aminouridine

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CAS 2149-76-0: 5-aminouridine

5-Aminouridine

Ref: TM-T13511

5-Aminouridine

Ref: 54-BUP10299

5-Aminouridine

Ref: 3D-NA163143