NAGIOS: RODERIC FUNCIONANDO

2,3,9- and 2,3,11-Trisubstituted tetrahydroprotoberberines as D2 dopaminergic ligands

Repositori DSpace/Manakin

Valencià Castellano

Inici
Investigació
e-prints
23 - Química
Visualitza element

IMPORTANT: Aquest repositori està en una versió antiga des del 3/12/2023. La nova instal.lació está en https://roderic.uv.es/

2,3,9- and 2,3,11-Trisubstituted tetrahydroprotoberberines as D2 dopaminergic ligands

Mostra el registre parcial de l'element

dc.contributor.author	Párraga Vidal, Javier
dc.contributor.author	Cabedo Escrig, Nuria
dc.contributor.author	Andujar, Sebastián
dc.contributor.author	Piqueras Ruiz, Laura
dc.contributor.author	Moreno Gálvez, Laura
dc.contributor.author	Galán Morant, Abraham
dc.contributor.author	Angelina, Emilio
dc.contributor.author	Enriz, Ricardo D.
dc.contributor.author	Ivorra Insa, María Dolores
dc.contributor.author	Sanz Ferrando, María Jesús
dc.contributor.author	Cortés Martínez, Diego M.
dc.date.accessioned	2020-05-07T10:12:27Z
dc.date.available	2020-05-07T10:12:27Z
dc.date.issued	2013
dc.identifier.citation	Párraga Vidal, Javier Cabedo Escrig, Nuria Andujar, Sebastián Piqueras Ruiz, Laura Moreno Gálvez, Laura Galán Morant, Abraham Angelina, Emilio Enriz, Ricardo D. Ivorra Insa, María Dolores Sanz Ferrando, María Jesús Cortés Martínez, Diego M. 2013 2,3,9- and 2,3,11-Trisubstituted tetrahydroprotoberberines as D2 dopaminergic ligands European Journal of Medicinal Chemistry 68C 150 166
dc.identifier.uri	https://hdl.handle.net/10550/74521
dc.description.abstract	Dopamine-mediated neurotransmission plays an important role in relevant psychiatric and neurological disorders. Nowadays, there is an enormous interest in the development of new dopamine receptors (DR) acting drugs as potential new targets for the treatment of schizophrenia or Parkinson's disease. Previous studies have revealed that isoquinoline compounds such as tetrahydroisoquinolines (THIQs) and tetrahydroprotoberberines (THPBs) can behave as selective D2 dopaminergic alkaloids since they share structural similarities with dopamine. In the present study we have synthesized eleven 2,3,9- and 2,3,11-trisubstituted THPB compounds (six of them are described for the first time) and evaluated their potential dopaminergic activity. Binding studies on rat striatal membranes were used to evaluate their affinity and selectivity towards D1 and D2 DR and establish the structure-activity relationship (SAR) as dopaminergic agents. In general, all the tested THPBs with protected phenolic hydroxyls showed a lower affinity for D1 and D2 DR than their corresponding homologues with free hydroxyl groups. In previous studies in which dopaminergic affinity of 1-benzyl-THIQs (BTHIQs) was evaluated, the presence of a Cl into the A-ring resulted in increased affinity and selectivity towards D2 DR. This is in contrast with the current study since the existence of a chlorine atom into the A-ring of the THPBs caused increased affinity for D1 DR but dramatically reduced the selectivity for D2 DR. An OH group in position 9 of the THPB (9f) resulted in a higher affinity for DR than its homologue with an OH group in position 11 (9e) (250 fold for D2 DR). None of the compounds showed any cytotoxicity in freshly isolated human neutrophils. A molecular modelling study of three representative THPBs was carried out. The combination of MD simulations with DFT calculations provided a clear picture of the ligand binding interactions from a structural and energetic point of view. Therefore, it is likely that compound 9d (2,3,9-trihydroxy-THPB) behave as D2 DR agonist since serine residues cluster are crucial for agonist binding and receptor activation.
dc.language.iso	eng
dc.relation.ispartof	European Journal of Medicinal Chemistry, 2013, vol. 68C, p. 150 -166
dc.subject	Química orgànica
dc.subject	Dopamina Receptors
dc.subject	Alcaloides
dc.subject	Compostos orgànics Síntesi
dc.title	2,3,9- and 2,3,11-Trisubstituted tetrahydroprotoberberines as D2 dopaminergic ligands
dc.type	journal article	es_ES
dc.date.updated	2020-05-07T10:12:27Z
dc.identifier.doi	10.1016/j.ejmech.2013.07.036
dc.identifier.idgrec	095263
dc.rights.accessRights	open access	es_ES