625446-78-8Relevant articles and documents
Identification and structure-based optimization of novel dihydropyrones as potent HCV RNA polymerase inhibitors
Li, Hui,Tatlock, John,Linton, Angelica,Gonzalez, Javier,Borchardt, Allen,Dragovich, Peter,Jewell, Tanya,Prins, Tom,Zhou, Ru,Blazel, Julie,Parge, Hans,Love, Robert,Hickey, Michael,Doan, Chau,Shi, Stephanie,Duggal, Rohit,Lewis, Cristina,Fuhrman, Shella
, p. 4834 - 4838 (2007/10/03)
A novel class of non-nucleoside HCV NS5B polymerase inhibitors has been identified from screening. A co-crystal structure revealed an allosteric binding site in the protein that required a unique conformational change to accommodate inhibitor binding. Her
INHIBITORS OF HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE, AND COMPOSITIONS AND TREATMENTS USING THE SAME
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Page 338, (2008/06/13)
The invention relates to compounds of the formula (I) and to pharmaceutically acceptable salts, solvates, prodrugs and metabolites thereof, wherein W, Z, R1and R2, are as defined herein. The invention also relates to methods of treating Hepatitis C virus in mammals by administering the compounds of formula (I), and to pharmaceutical compositions for treating such disorders, which contain the compounds of formula (I). The invention also relates to methods of preparing the compounds of formula (I).