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      Discovery of a novel series of DHODH inhibitors by a docking procedure and QSAR refinement.

      Bioorganic & Medicinal Chemistry Letters
      Binding Sites, drug effects, physiology, Enzyme Inhibitors, chemistry, metabolism, pharmacology, Humans, Oxidoreductases Acting on CH-CH Group Donors, antagonists & inhibitors, Quantitative Structure-Activity Relationship

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          Abstract

          A novel series of DHODH inhibitors was developed based on a lead which was obtained by a docking procedure and a medicinal chemistry exploration. The activity of the initial lead was improved by a QSAR method to yield low nanomolar inhibitors.

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