Peptidyl inhibitors of viral proteases

作者: Philip Stephen Jones , David Nigel Hurst , Tony Michael Raynham , Paul Brittain Kay , Michael Richard Attwood

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摘要: The invention provides amino acid derivatives of the formula ##STR1## wherein E represents CHO or B(OH) 2 ; R 1 lower alkyl (optionally substituted by halo, cyano, alkylthio, aryl-lower aryl heteroaryl), alkenyl alkynyl; optionally hydroxy, carboxy, aryl, aminocarbonyl cycloalkyl; and 3 hydrogen alkyl; together represent di- trimethylene hydroxy; 4 cycloalkyl, cyano-lower alkylthio alkylthio), alkenyl, 5 alkylthio) 6 7 cycloalkyl) 8 carboxy aryl; 9 alkylcarbonyl, carboxy-lower arylcarbonyl, alkylsulphonyl, arylsulphonyl, alkoxycarbonyl al koxycarbonyl, salts acidic compounds I with bases, which are viral proteinase inhibitors useful as antiviral agents, especially for treatment prophylaxis infections caused Hepatitis C, G human GB viruses.

参考文章(4)
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Christian Steinkühler, Frank Narjes, Marina Taliani, Licia Tomei, Raffaele De Francesco, Elisabetta Bianchi, Andrea Urbani, Antonello Pessi, Methodology to produce, purify and assay polypeptides with the proteolytic activity of the hcv ns3 protease ,(1996)