The identification of novel acid isostere based inhibitors of the VPS10P family sorting receptor Sortilin

Using fragment based and structure based drug discovery strategies, a series of novel Sortilin inhibitors has been identified. The inhibitors are based on the N-substituted 1,2,3-triazol-4-one/ol heterocyclic template. X-ray crystallography shows that the 1,2,3-triazol-4-one/ol acts as a carboxylic...

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2017-06, Vol.27 (11), p.2629-2633
Hauptverfasser: Andersen, Jacob Lauwring, Lindberg, Samsa, Langgård, Morten, Maltas, Philip J., Rønn, Lars Christian Biilmann, Bundgaard, Christoffer, Strandbygaard, Dorthe, Thirup, Søren, Watson, Stephen P
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Sprache:eng
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Zusammenfassung:Using fragment based and structure based drug discovery strategies, a series of novel Sortilin inhibitors has been identified. The inhibitors are based on the N-substituted 1,2,3-triazol-4-one/ol heterocyclic template. X-ray crystallography shows that the 1,2,3-triazol-4-one/ol acts as a carboxylic acid isostere, making a bi-dentate interaction with an arginine residue of Sortilin, an interaction which has not been previously characterised for this heterocycle. [Display omitted] Using fragment based and structure based drug discovery strategies a series of novel Sortilin inhibitors has been identified. The inhibitors are based on the N-substituted 1,2,3-triazol-4-one/ol heterocyclic template. X-ray crystallography shows that the 1,2,3-triazol-4-one/ol acts as a carboxylic acid isostere, making a bi-dentate interaction with an arginine residue of Sortilin, an interaction which has not been previously characterised for this heterocycle.
ISSN:0960-894X
1464-3405
DOI:10.1016/j.bmcl.2017.02.028