915023-64-2Relevant academic research and scientific papers
6-Hydrazinopurine 2′-methyl ribonucleosides and their 5′-monophosphate prodrugs as potent hepatitis C virus inhibitors
Gunic, Esmir,Chow, Suetying,Rong, Frank,Ramasamy, Kanda,Raney, Anneke,Yunzhi Li, David,Huang, Jingfan,Hamatake, Robert K.,Hong, Zhi,Girardet, Jean-Luc
, p. 2456 - 2458 (2008/02/03)
A series of 6-hydrazinopurine 2′-methyl ribonucleosides was synthesized and tested for its inhibitory activity against the hepatitis C virus (HCV). The lack of antiviral activity of these nucleosides was associated with a poor affinity for adenosine kinase, which prompted us to synthesize several of their 5′-monophosphate prodrugs. Some of these prodrugs exhibited more than 1000-fold improvement in anti-HCV activity when compared to their parent nucleosides (EC50 of 24 nM vs 92 μM for the parent).
6-HYDRAZINOPURINE 2'-METHYL RIBONUCLEOSIDES AND NUCLEOTIDES FOR TREATMENT OF HCV
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Page/Page column 8, (2008/06/13)
Compounds of formula I, are provided, which are useful as inhibitors of hepatitis C virus.
