Macrocyclic inhibitors of flaviviridae viruses

Provided are compounds of Formula (I) and pharmaceutically acceptable salts and esters thereof. The compounds, compositions, and methods provided are useful for the treatment of Flaviviridae virus infections, particularly hepatitis C infections. In one embodiment the compound is (E)-(1S,13R,14R,17S,...

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Main Authors SANVOISIN JONATHAN, WATT GREGORY M, FLIRI HANS G, LAZARIDES LINOS, KEATS ANDREW J, MACKMAN RICHARD L, APPLEBY TODD, PETTIT SIMON N, STEADMAN VICTORIA A, POULLENNEC KARINE G
Format Patent
LanguageEnglish
Published 31.07.2015
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Summary:Provided are compounds of Formula (I) and pharmaceutically acceptable salts and esters thereof. The compounds, compositions, and methods provided are useful for the treatment of Flaviviridae virus infections, particularly hepatitis C infections. In one embodiment the compound is (E)-(1S,13R,14R,17S,20S)-20-(3-Hydroxy-benzyl)-17-isopropyl-13-methoxy-14-methyl-3-oxa-6-thia-16,19,22,26-tetraazatricyclo[20.3.1.1*5,8*]heptacosa-5(27),7,9-triene-2,15,18,21-tetraone
Bibliography:Application Number: NZ20110612159