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A solid-phase combinatorial approach for indoloquinolizidine-peptides with high affinity at D1 and D2 dopamine receptors

Research output: Contribution to journalArticle

  • Anabel Molero
  • Marc Vendrell
  • Jordi Bonaventura
  • Julian Zachmann
  • Laura Lopez
  • Leonardo Pardo
  • Carme Lluis
  • Antoni Cortes
  • Fernando Albericio
  • Vicent Casado
  • Miriam Royo

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http://www.sciencedirect.com/science/article/pii/S0223523415300155#
Original languageEnglish
Pages (from-to)173–180
Number of pages8
JournalEuropean Journal of Medicinal Chemistry
Volume97
DOIs
Publication statusPublished - 5 Jun 2015

Abstract

Ligands acting at multiple dopamine receptors hold potential as therapeutic agents for a number of neurodegenerative disorders. Specifically, compounds able to bind at D1R and D2R with high affinity could restore the effects of dopamine depletion and enhance motor activation on degenerated nigrostriatal dopaminergic systems. We have directed our research towards the synthesis and characterisation of heterocycle-peptide hybrids based on the indolo[2,3-a]quinolizidine core. This privileged structure is a water-soluble and synthetically accessible scaffold with affinity for diverse GPCRs. Herein we have prepared a solid-phase combinatorial library of 80 indoloquinolizidine-peptides to identify compounds with enhanced binding affinity at D2R, a receptor that is crucial to re-establish activity on dopamine-depleted degenerated GABAergic neurons. We applied computational tools and high-throughput screening assays to identify 9a{1,3,3} as a ligand for dopamine receptors with nanomolar affinity and agonist activity at D2R. Our results validate the application of indoloquinolizidine-peptide combinatorial libraries to fine-tune the pharmacological profiles of multiple ligands at D1 and D2 dopamine receptors.

    Research areas

  • Privileged scaffolds; , Solid-phase synthesis, GPCRs, Neurodegenerative diseases, Heterocycles

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