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 2′-Deoxy-β-L-uridine Chemical Structure 2'-Deoxy-L-Uridine

Catalog NO.: L-DNS-004 | CAS NO.: 31501-19-6 | Brand: BIOCAXIS

Category

Nucleosides & Nucleotides, 2’-deoxy

Synonyms:

9-(2-Deoxy-b-L-erythro-pentofuranosyl) uracil

 

Molecular Formula

C9H12N2O5

Molecular Weight

228.20

 

General description

2'-Deoxy-β-L-uridine is a nucleoside analogue and a specific substrate for the viral enzyme, shows no stereospecificity against herpes simplex 1 (HSV1) thymidine kinase (TK). 2-Deoxy-β-L-uridine exerts antiviral activity via the interaction of 5'-triphosphates with the viral DNA polymerase.

2'-Deoxy-L-uridine is a nucleoside that is found in the human body. It phosphorylates l-thymidine, which is a natural substrate, and this reaction prevents the formation of diphosphate from d-ribose 5'-monophosphate. 2'-Deoxy-L-uridine is an exogenous substance that inhibits cell growth by affecting protein synthesis and DNA replication. 2'-Deoxy-L-uridine has been shown to be more efficient than wild type uridine in inhibiting cell growth in vitro at concentrations of 1 mM or greater. The enantiomers of 2'-deoxy-L-uridine affect cell growth differently, with the (R)-enantiomer being more potent than the (S)-enantiomer.

 

 

 

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