Macrocyclic proline derived hcv serine protease inhibitors
Abstract
The present invention discloses compounds of Formula I or pharmaceutically acceptable salts, esters, or prodrugs thereof: which inhibit serine protease activity, particularly the activity of hepatitis C virus (HCV) NS3-NS4A protease. Consequently, the compounds of the present invention interfere with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HCV infection. The invention also relates to methods of treating an HCV infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention.
Claims
exact text as granted — not AI-modified1 - 26 . (canceled)
27 . A compound selected from the group consisting of:
28 . The compound of claim 1 , wherein the compound is:
29 . The compound of claim 1 , wherein the compound is:
30 . The compound of claim 1 , wherein the compound is:Join the waitlist — get patent alerts
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