Inhibitors of serine proteases, particularly HCV NS3-NS4A...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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Details

C546S079000, C546S085000, C546S112000, C548S134000, C548S146000, C548S182000, C548S225000, C548S250000, C548S262200, C548S452000, C548S465000, C514S292000, C514S299000

Reexamination Certificate

active

10412600

ABSTRACT:
The present invention relates to compounds that inhibit serine protease activity, particularly the activity of hepatitis C virus NS3-NS4A protease. As such, they act by interfering with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The invention further relates to compositions comprising these compounds either for ex vivo use or for administration to a patient suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a patient by administering a composition comprising a compound of this invention. The invention further relates to processes for preparing these compounds.

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Han, Wei et al., “α-Ketoamides, α-Ketoesters and α-Diketones as HCV NS3 Protease Inhibitors,” Bioorganic & Medicinal Chemistry Letters, 2000, vol. 10, No. 8, pp. 711-713.

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