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Discovery and in vitro Evaluation of Novel Serotonin 5-HT 2A Receptor Ligands Identified Through Virtual Screening.

Authors :
Zięba A
Bartuzi D
Stępnicki P
Matosiuk D
Wróbel TM
Laitinen T
Castro M
Kaczor AA
Source :
ChemMedChem [ChemMedChem] 2024 Jul 15; Vol. 19 (14), pp. e202400080. Date of Electronic Publication: 2024 May 29.
Publication Year :
2024

Abstract

The 5-HT <subscript>2A</subscript> receptor is a molecular target of high pharmacological importance. Ligands of this protein, particularly atypical antipsychotics, are useful in the treatment of numerous mental disorders, including schizophrenia and major depressive disorder. Structure-based virtual screening using a 5-HT <subscript>2A</subscript> receptor complex was performed to identify novel ligands for the 5-HT <subscript>2A</subscript> receptor, serving as potential antidepressants. From the Enamine screening library, containing over 4 million compounds, 48 molecules were selected for subsequent experimental validation. These compounds were tested against the 5-HT <subscript>2A</subscript> receptor in radioligand binding assays. From the tested batch, six molecules were identified as ligands of the main molecular target and were forwarded to a more detailed in vitro profiling. This included radioligand binding assays at 5-HT <subscript>1A</subscript> , 5-HT <subscript>7</subscript> , and D <subscript>2</subscript> receptors and functional studies at 5-HT <subscript>2A</subscript> receptors. These compounds were confirmed to show a binding affinity for at least one of the targets tested in vitro. The success rate for the inactive template-based screening reached 17 %, while it was 9 % for the active template-based screening. Similarity and fragment analysis indicated the structural novelty of the identified compounds. Pharmacokinetics for these molecules was determined using in silico approaches.<br /> (© 2024 Wiley-VCH GmbH.)

Details

Language :
English
ISSN :
1860-7187
Volume :
19
Issue :
14
Database :
MEDLINE
Journal :
ChemMedChem
Publication Type :
Academic Journal
Accession number :
38619283
Full Text :
https://doi.org/10.1002/cmdc.202400080