Title of article :
Identification and structure-based optimization of novel dihydropyrones as potent HCV RNA polymerase inhibitors
Author/Authors :
Hui Li، نويسنده , , John Tatlock، نويسنده , , M. Angelica Linton، نويسنده , , Javier Gonzalez، نويسنده , , Allen Borchardt، نويسنده , , Peter Dragovich، نويسنده , , Tanya Jewell، نويسنده , , Tom Prins، نويسنده , , Ru Zhou، نويسنده , , Julie Blazel، نويسنده , , Hans Parge، نويسنده , , Robert Love، نويسنده , , Michael Hickey، نويسنده , , Chau Doan، نويسنده , , Stephanie Shi، نويسنده , , Rohit Duggal، نويسنده , , Cristina Lewis، نويسنده , , Shella Fuhrman، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2006
Pages :
5
From page :
4834
To page :
4838
Abstract :
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. Herein we report the structure–activity relationships (SARs) of this novel class of dihydropyrone-containing compounds that show potent inhibitory activities against the HCV RNA polymerase in biochemical assays.
Keywords :
HCV Polymerase , Dihydropyrone , structure-based drug design
Journal title :
Bioorganic & Medicinal Chemistry Letters
Serial Year :
2006
Journal title :
Bioorganic & Medicinal Chemistry Letters
Record number :
797289
Link To Document :
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