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Synthesis, Structural and Behavioral Studies of Indole Derivatives D2AAK5, D2AAK6 and D2AAK7 as Serotonin 5-HT(1A) and 5-HT(2A) Receptor Ligands
Serotonin receptors are involved in a number of physiological functions and regulate aggression, anxiety, appetite, cognition, learning, memory, mood, nausea, sleep, and thermoregulation. Here we report synthesis and detailed structural and behavioral studies of three indole derivatives: D2AAK5, D2A...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823611/ https://www.ncbi.nlm.nih.gov/pubmed/36615578 http://dx.doi.org/10.3390/molecules28010383 |
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author | Kaczor, Agnieszka A. Kędzierska, Ewa Wróbel, Tomasz M. Grudzińska, Angelika Pawlak, Angelika Laitinen, Tuomo Bartyzel, Agata |
author_facet | Kaczor, Agnieszka A. Kędzierska, Ewa Wróbel, Tomasz M. Grudzińska, Angelika Pawlak, Angelika Laitinen, Tuomo Bartyzel, Agata |
author_sort | Kaczor, Agnieszka A. |
collection | PubMed |
description | Serotonin receptors are involved in a number of physiological functions and regulate aggression, anxiety, appetite, cognition, learning, memory, mood, nausea, sleep, and thermoregulation. Here we report synthesis and detailed structural and behavioral studies of three indole derivatives: D2AAK5, D2AAK6, and D2AAK7 as serotonin 5-HT(1A) and 5-HT(2A) receptor ligands. X-ray studies revealed that the D2AAK5 compound crystallizes in centrosymmetric triclinic space group with one molecule in the asymmetric unit. The main interaction between the ligands and the receptors is the salt bridge between the protonatable nitrogen atom of the ligands and the conserved Asp (3.32) of the receptors. The complexes were stable in the molecular dynamic simulations. MD revealed that the studied ligands are relatively stable in their binding sites, with the exception of D2AAK7 in the serotonin 5-HT(1A) receptor. D2AAK7 exerts anxiolytic activity in the EPM test, while D2AAK5 has a beneficial effect on the memory processes in the PA test. |
format | Online Article Text |
id | pubmed-9823611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98236112023-01-08 Synthesis, Structural and Behavioral Studies of Indole Derivatives D2AAK5, D2AAK6 and D2AAK7 as Serotonin 5-HT(1A) and 5-HT(2A) Receptor Ligands Kaczor, Agnieszka A. Kędzierska, Ewa Wróbel, Tomasz M. Grudzińska, Angelika Pawlak, Angelika Laitinen, Tuomo Bartyzel, Agata Molecules Article Serotonin receptors are involved in a number of physiological functions and regulate aggression, anxiety, appetite, cognition, learning, memory, mood, nausea, sleep, and thermoregulation. Here we report synthesis and detailed structural and behavioral studies of three indole derivatives: D2AAK5, D2AAK6, and D2AAK7 as serotonin 5-HT(1A) and 5-HT(2A) receptor ligands. X-ray studies revealed that the D2AAK5 compound crystallizes in centrosymmetric triclinic space group with one molecule in the asymmetric unit. The main interaction between the ligands and the receptors is the salt bridge between the protonatable nitrogen atom of the ligands and the conserved Asp (3.32) of the receptors. The complexes were stable in the molecular dynamic simulations. MD revealed that the studied ligands are relatively stable in their binding sites, with the exception of D2AAK7 in the serotonin 5-HT(1A) receptor. D2AAK7 exerts anxiolytic activity in the EPM test, while D2AAK5 has a beneficial effect on the memory processes in the PA test. MDPI 2023-01-02 /pmc/articles/PMC9823611/ /pubmed/36615578 http://dx.doi.org/10.3390/molecules28010383 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kaczor, Agnieszka A. Kędzierska, Ewa Wróbel, Tomasz M. Grudzińska, Angelika Pawlak, Angelika Laitinen, Tuomo Bartyzel, Agata Synthesis, Structural and Behavioral Studies of Indole Derivatives D2AAK5, D2AAK6 and D2AAK7 as Serotonin 5-HT(1A) and 5-HT(2A) Receptor Ligands |
title | Synthesis, Structural and Behavioral Studies of Indole Derivatives D2AAK5, D2AAK6 and D2AAK7 as Serotonin 5-HT(1A) and 5-HT(2A) Receptor Ligands |
title_full | Synthesis, Structural and Behavioral Studies of Indole Derivatives D2AAK5, D2AAK6 and D2AAK7 as Serotonin 5-HT(1A) and 5-HT(2A) Receptor Ligands |
title_fullStr | Synthesis, Structural and Behavioral Studies of Indole Derivatives D2AAK5, D2AAK6 and D2AAK7 as Serotonin 5-HT(1A) and 5-HT(2A) Receptor Ligands |
title_full_unstemmed | Synthesis, Structural and Behavioral Studies of Indole Derivatives D2AAK5, D2AAK6 and D2AAK7 as Serotonin 5-HT(1A) and 5-HT(2A) Receptor Ligands |
title_short | Synthesis, Structural and Behavioral Studies of Indole Derivatives D2AAK5, D2AAK6 and D2AAK7 as Serotonin 5-HT(1A) and 5-HT(2A) Receptor Ligands |
title_sort | synthesis, structural and behavioral studies of indole derivatives d2aak5, d2aak6 and d2aak7 as serotonin 5-ht(1a) and 5-ht(2a) receptor ligands |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823611/ https://www.ncbi.nlm.nih.gov/pubmed/36615578 http://dx.doi.org/10.3390/molecules28010383 |
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