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Early Viral Entry Assays for the Identification and Evaluation of Antiviral Compounds
Published on: October 29, 2015
Inhibitors of hepatitis C virus NS3.4A protease 1. Non-charged tetrapeptide variants
Robert B Perni1, Shawn D Britt, John C Court
1Vertex Pharmaceuticals Inc., 130 Waverly Street, Cambridge, MA 02139, USA. robert_perni@vrtx.com
Bioorganic & Medicinal Chemistry Letters
|November 1, 2003
Abstract:
Tetrapeptide-based peptidomimetic compounds have been shown to effectively inhibit the hepatitis C virus NS3.4A protease without the need of a charged functionality. An aldehyde is used as a prototype reversible electrophilic warhead. The SAR of the P1 and P2 inhibitor positions is discussed.
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