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Inhibition of Dengue virus and West Nile virus proteases by click chemistry-derived benz[d]isothiazol-3(2H)-one derivatives.
Tiew, Kok-Chuan; Dou, Dengfeng; Teramoto, Tadahisa; Lai, Huiguo; Alliston, Kevin R; Lushington, Gerald H; Padmanabhan, R; Groutas, William C.
Affiliation
  • Tiew KC; Department of Chemistry, Wichita State University, Wichita, KS 67260, USA.
Bioorg Med Chem ; 20(3): 1213-21, 2012 Feb 01.
Article in En | MEDLINE | ID: mdl-22249124
ABSTRACT
Two click chemistry-derived focused libraries based on the benz[d]isothiazol-3(2H)-one scaffold were synthesized and screened against Dengue virus and West Nile virus NS2B-NS3 proteases. Several compounds (4l, 7j-n) displayed noteworthy inhibitory activity toward Dengue virus NS2B-NS3 protease in the absence and presence of added detergent. These compounds could potentially serve as a launching pad for a hit-to-lead optimization campaign.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antiviral Agents / Peptide Hydrolases / Protease Inhibitors / West Nile virus / Dengue Virus Limits: Humans Language: En Journal: Bioorg Med Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2012 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antiviral Agents / Peptide Hydrolases / Protease Inhibitors / West Nile virus / Dengue Virus Limits: Humans Language: En Journal: Bioorg Med Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2012 Document type: Article Affiliation country: United States