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      Development of 3,5-dinitrobenzoate-based 5-lipoxygenase inhibitors.

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          Abstract

          Human 5-lipoxygenase (5-LOX) is a well-validated target for anti-inflammatory therapy. Development of novel 5-LOX inhibitors with higher activities is highly demanded. In previous study, we have built a model for the active conformation of human 5-LOX, and identified naphthalen-1-yl 3,5-dinitrobenzoate (JMC-4) as a 5-LOX inhibitor by virtual screening. In the present work, 3,5-dinitrobenzoate-based 5-lipoxygenase inhibitors were developed. Twenty aryl 3,5-dinitrobenzoates, N-aryl 3,5-dinitrobenzamides and analogues were designed and synthesized. Several of them were found with significantly increased activities according to cell-free assay and human whole blood assay. The structure-activity relationship study may provide useful insights for designing effective 5-LOX inhibitors.

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          Author and article information

          Journal
          Bioorg. Med. Chem.
          Bioorganic & medicinal chemistry
          Elsevier BV
          1464-3391
          0968-0896
          Apr 15 2014
          : 22
          : 8
          Affiliations
          [1 ] BNLMS, State Key Laboratory for Structural Chemistry of Unstable and Stable Species, College of Chemistry and Molecular Engineering, Center for Quantitative Biology, Peking University, Beijing 100871, China.
          [2 ] BNLMS, State Key Laboratory for Structural Chemistry of Unstable and Stable Species, College of Chemistry and Molecular Engineering, Center for Quantitative Biology, Peking University, Beijing 100871, China. Electronic address: liuying@pku.edu.cn.
          Article
          S0968-0896(14)00181-3
          10.1016/j.bmc.2014.03.008
          24685113
          ff4d8705-ddb2-458e-a07a-d07debe5a49e
          History

          Cell-free assay,SAR study,3,5-Dinitrobenzoate,5-Lipoxygenase inhibitors,Human whole blood assay

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