Cyclic monophosphate prodrugs of base-modified 2′-C-methyl ribonucleosides as potent inhibitors of hepatitis C virus RNA replication-Reference-Cited by-同舟云学术

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Cyclic monophosphate prodrugs of base-modified 2′-C-methyl ribonucleosides as potent inhibitors of hepatitis C virus RNA replication

Published:2007-05 Issue:9 Volume:17 Page:2452-2455
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Gunic Esmir,Girardet Jean-Luc,Ramasamy Kanda,Stoisavljevic-Petkov Vesna,Chow Suetying,Yeh Li-Tain,Hamatake Robert K.,Raney Anneke,Hong Zhi

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference10 articles.

1. Isolation of a cDNA cLone Derived from a Blood-Borne Non-A, Non-B Viral Hepatitis Genome

2. Epidemiology of Hepatitis C: Geographic Differences and Temporal Trends

3. Structure−Activity Relationship of Heterobase-Modified 2‘-C-Methyl Ribonucleosides as Inhibitors of Hepatitis C Virus RNA Replication

4. Synthesis and Pharmacokinetics of Valopicitabine (NM283), an Efficient Prodrug of the Potent Anti-HCV Agent 2‘-C-Methylcytidine

5. Inhibition of Hepatitis C Virus RNA Replication by 2′-Modified Nucleoside Analogs

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