Hcv ns-3 serine protease inhibitors

C - Chemistry – Metallurgy – 07 – K

Patent

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Details

C07K 5/02 (2006.01) A61K 31/47 (2006.01) A61P 31/12 (2006.01) C07D 207/16 (2006.01) C07D 401/12 (2006.01) C07D 405/14 (2006.01) C07D 409/14 (2006.01) C07D 413/14 (2006.01) C07D 417/14 (2006.01) C07D 487/04 (2006.01)

Patent

CA 2552317

Compounds of the formula (F) where the variables are as defined in the specification inhibit the NS3 protease of flavivirus sych as hepatitis C virus (HCV). The compounds comprise a novel linkage between a heterocyclic P2 unit and those portions of the inhibitor more distal to the nominal cleavage site of the native substrate, which linkage reverses the orientation of peptidic bonds on the distal side relative to those proximal to the cleavage site.

L'invention concerne des composés représentés par la formule (F) dans laquelle les variables sont telles que définies dans les spécifications, inhibant la protéase NS3 d'un flavivirus tel que le virus de l'hépatite C (VHC). Ces composés présentent une nouvelle liaison entre une unité hétérocyclique P2 et les parties de l'inhibiteur plus distales que le site de clivage nominal du substrat natif, ladite liaison inversant l'orientation des liaisons peptidiques situées sur le côté distal par rapport à celles situées de manière proximale par rapport au site de clivage.

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