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Structure-metabolism relationships in human-AOX: Chemical insights from a large database of aza-aromatic and amide compounds.
Lepri, Susan; Ceccarelli, Martina; Milani, Nicolò; Tortorella, Sara; Cucco, Andrea; Valeri, Aurora; Goracci, Laura; Brink, Andreas; Cruciani, Gabriele.
Affiliation
  • Lepri S; Department of Chemistry, Biology and Biotechnology, University of Perugia, 06123 Perugia, Italy.
  • Ceccarelli M; Department of Chemistry, Biology and Biotechnology, University of Perugia, 06123 Perugia, Italy.
  • Milani N; Department of Chemistry, Biology and Biotechnology, University of Perugia, 06123 Perugia, Italy.
  • Tortorella S; Department of Chemistry, Biology and Biotechnology, University of Perugia, 06123 Perugia, Italy.
  • Cucco A; Department of Chemistry, Biology and Biotechnology, University of Perugia, 06123 Perugia, Italy.
  • Valeri A; Department of Chemistry, Biology and Biotechnology, University of Perugia, 06123 Perugia, Italy.
  • Goracci L; Department of Chemistry, Biology and Biotechnology, University of Perugia, 06123 Perugia, Italy.
  • Brink A; Roche Pharma Research and Early Development, Drug Disposition and Safety, Roche Innovation Center Basel, F. Hoffmann-La Roche, Ltd., 4070 Basel, Switzerland.
  • Cruciani G; Department of Chemistry, Biology and Biotechnology, University of Perugia, 06123 Perugia, Italy; gabriele.cruciani@unipg.it.
Proc Natl Acad Sci U S A ; 114(16): E3178-E3187, 2017 04 18.
Article in En | MEDLINE | ID: mdl-28373537
Aldehyde oxidase (AOX) is a metabolic enzyme catalyzing the oxidation of aldehyde and aza-aromatic compounds and the hydrolysis of amides, moieties frequently shared by the majority of drugs. Despite its key role in human metabolism, to date only fragmentary information about the chemical features responsible for AOX susceptibility are reported and only "very local" structure-metabolism relationships based on a small number of similar compounds have been developed. This study reports a more comprehensive coverage of the chemical space of structures with a high risk of AOX phase I metabolism in humans. More than 270 compounds were studied to identify the site of metabolism and the metabolite(s). Both electronic [supported by density functional theory (DFT) calculations] and exposure effects were considered when rationalizing the structure-metabolism relationship.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aza Compounds / Aldehyde Oxidase / Databases, Pharmaceutical / Amides / Hydrocarbons, Aromatic Limits: Humans Language: En Journal: Proc Natl Acad Sci U S A Year: 2017 Type: Article Affiliation country: Italy

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aza Compounds / Aldehyde Oxidase / Databases, Pharmaceutical / Amides / Hydrocarbons, Aromatic Limits: Humans Language: En Journal: Proc Natl Acad Sci U S A Year: 2017 Type: Article Affiliation country: Italy