Structure-Based Optimization of Coumarin hA(3) Adenosine Receptor Antagonists

• Tipo: Artigo em Revista Científica Internacional
• Data: 2020

Autores

Matos, MJ (Autor) FCUP; Vilar, S (Autor) Outra; Vazquez Rodriguez, S (Autor) Outra; Kachler, S (Autor) Outra; Klotz, KN (Autor) Outra; Buccioni, M (Autor) Outra; Delogu, G (Autor) Outra; Santana, L (Autor) Outra; Uriarte, E (Autor) Outra; Fernanda Borges (Autor) FCUP

Revista

Título: Journal of Medicinal Chemistry

Vol. 63

Páginas: 2577-2587

ISSN: 0022-2623

Editora: American Chemical Society

Indexação

ISI Web of Knowledge - 15 Citações

Scopus - 14 Citações

Outras Informações

ID Authenticus: P-00S-169

DOI: 10.1021/acs.jmedchem.9b01572

Abstract (EN): Adenosine receptors participate in many physiological functions. Molecules that may selectively interact with one of the receptors are favorable multifunctional chemical entities to treat or decelerate the evolution of different diseases. 3-Arylcoumarins have already been studied as neuroprotective agents by our group. Here, differently 8-substituted 3-arylcoumarins are complementarily studied as ligands of adenosine receptors, performing radioligand binding assays. Among the synthesized compounds, selective A(3) receptor antagonists were found. 3-(4-Bromophenyl)-8-hydroxycoumarin (compound 4) displayed the highest potency and selectivity as A(3) receptor antagonist (K-i = 258 nM). An analysis of its X-ray diffraction provided detailed information on its structure. Further evaluation of a selected series of compounds indicated that it is the nature and position of the substituents that determine their activity and selectivity. Theoretical modeling calculations corroborate and explain the experimental data, suggesting this novel scaffold can be involved in the generation of candidates as multitarget drugs.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 11