
CAS 40093-94-5
:4-Amino-1-[(2S,4R,5S)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]pyrimidin-2(1H)-one
Description:
4-Amino-1-[(2S,4R,5S)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]pyrimidin-2(1H)-one, with CAS number 40093-94-5, is a chemical compound that features a pyrimidine ring substituted with an amino group and a tetrahydrofuran moiety. This compound is characterized by its structural complexity, which includes multiple functional groups such as hydroxyl and amino groups, contributing to its potential biological activity. It is often studied in the context of medicinal chemistry, particularly for its role as a nucleoside analog or in the development of antiviral or anticancer agents. The presence of the tetrahydrofuran ring suggests that it may exhibit interesting stereochemical properties, which can influence its interaction with biological targets. Additionally, the compound's solubility, stability, and reactivity are influenced by its functional groups, making it a subject of interest in pharmaceutical research. Overall, this compound exemplifies the intricate relationship between molecular structure and biological function in drug design.
Formula:C9H13N3O4
InChI:InChI=1/C9H13N3O4/c10-7-1-2-12(9(15)11-7)8-3-5(14)6(4-13)16-8/h1-2,5-6,8,13-14H,3-4H2,(H2,10,11,15)/t5-,6+,8+/m1/s1
Synonyms:- Torcitabine
- L-dC
- Nv-02C
- beta-L-Deoxycytidine
- 4-Amino-1-(2-deoxy-beta-L-erythro-pentofuranosyl)pyrimidin-2(1H)-one
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Found 4 products.
2(1H)-Pyrimidinone, 4-amino-1-(2-deoxy-b-L-erythro-pentofuranosyl)-
CAS:Formula:C9H13N3O4Purity:95%Color and Shape:SolidMolecular weight:227.21722''-Deoxy-L-cytidine
CAS:Formula:C9H13N3O4Purity:≥ 99.0% (HPLC)Color and Shape:White to off-white powderMolecular weight:227.22Torcitabine
CAS:Torcitabine is useful against the hepatitis B virus.Formula:C9H13N3O4Color and Shape:SolidMolecular weight:227.222'-Deoxy-L-cytidine
CAS:<p>2'-Deoxy-L-cytidine is a nucleoside that is naturally found in the cells of E. coli K-12. It is an antioxidant compound that prevents lipid peroxidation and scavenges free radicals, which are generated by certain chemical reactions. 2'-Deoxy-L-cytidine has been shown to have antiviral potency in vitro, but its antiviral activity has not been evaluated in vivo. This compound also inhibits the growth of bacteria that are resistant to tetracycline, such as Mycobacterium tuberculosis and Helicobacter pylori. 2'-Deoxy-L-cytidine may cause drug interactions with other medications because it is metabolized by the CYP450 system and inhibits the activity of cytochrome P450 enzymes.</p>Formula:C9H13N3O4Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:227.22 g/mol



