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Vinylated linear P2 pyrimidinyloxyphenylglycine based inhibitors of the HCV NS3/4A protease and corresponding macrocycles

Lampa, Anna (author)
Uppsala universitet,Avdelningen för organisk farmaceutisk kemi
Alogheli, Hiba (author)
Uppsala universitet,Avdelningen för organisk farmaceutisk kemi
Ehrenberg, Angelica E. (author)
Uppsala universitet,Institutionen för kemi - BMC
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Åkerblom, Eva (author)
Uppsala universitet,Avdelningen för organisk farmaceutisk kemi
Svensson, Richard (author)
Uppsala universitet,Institutionen för farmaci
Artursson, Per (author)
Uppsala universitet,Institutionen för farmaci
Danielson, Helena (author)
Uppsala universitet,Biokemi
Karlén, Anders (author)
Uppsala universitet,Avdelningen för organisk farmaceutisk kemi
Sandström, Anja (author)
Uppsala universitet,Avdelningen för organisk farmaceutisk kemi
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 (creator_code:org_t)
Elsevier BV, 2014
2014
English.
In: Bioorganic & Medicinal Chemistry. - : Elsevier BV. - 0968-0896 .- 1464-3391. ; 22:23, s. 6595-6615
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • With three recent market approvals and several inhibitors in advanced stages of development, the hepatitis C virus (HCV) NS3/4A protease represents a successful target for antiviral therapy against hepatitis C. As a consequence of dealing with viral diseases in general, there are concerns related to the emergence of drug resistant strains which calls for development of inhibitors with an alternative binding-mode than the existing highly optimized ones. We have previously reported on the use of phenylglycine as an alternative P2 residue in HCV NS3/4A protease inhibitors. Herein, we present the synthesis, structure-activity relationships and in vitro pharmacokinetic characterization of a diverse series of linear and macrocyclic P2 pyrimidinyloxyphenylglycine based inhibitors. With access to vinyl substituents in P3, P2 and P1' positions an initial probing of macrocyclization between different positions, using ring-closing metathesis (RCM) could be performed, after addressing some synthetic challenges. Biochemical results from the wild type enzyme and drug resistant variants (e.g., R155 K) indicate that P3-P1' macrocyclization, leaving the P2 substituent in a flexible mode, is a promising approach. Additionally, the study demonstrates that phenylglycine based inhibitors benefit from p-phenylpyrimidinyloxy and m-vinyl groups as well as from the combination with an aromatic P1 motif with alkenylic P1' elongations. In fact, linear P2-P1' spanning intermediate compounds based on these fragments were found to display promising inhibitory potencies and drug like properties.

Subject headings

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Keyword

HCV
NS3
Protease inhibitors
Macrocyclization
Phenylglycine
Metathesis

Publication and Content Type

ref (subject category)
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