SERAAK2 as a Serotonin Receptor Ligand: Structural and Pharmacological In Vitro and In Vivo Evaluation

Serotonin receptors, in particular 5-HT<sub>1A</sub> and 5-HT<sub>2A</sub> receptors, are important molecular targets for the central nervous system (CNS) disorders, such as schizophrenia, depression, anxiety disorders, memory deficits, and many others. Here, we present structural and pharmacological evaluation of a serotonin receptor ligand, SERAAK2, identified in a structure-based virtual screening campaign. Molecular docking studies revealed that SERAAK2 binds with its molecular targets via Asp3.32 as the main anchoring point, which is typical for orthosteric ligands of aminergic GPCRs. Molecular dynamics simulations confirmed the stability of the ligand binding poses in the studied receptors. MMGBSA calculations were in accordance with the receptor in vitro binding affinity studies, which indicated that SERAAK2 is a potent ligand of 5-HT<sub>1A</sub> and 5-HT<sub>2A</sub> receptors. It was also found that SERAAK2 displays favorable ADMET parameters. The demonstrated anxiolytic- and antidepressant-like effects of SERAAK2 in animal models, which may involve its interaction with 5-HT<sub>1A</sub> receptors, warrant further studies to confirm these activities and elucidate the underlying mechanisms.

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Publication Details

Journal
Molecules
Published
2025-12-02
DOI
https://doi.org/10.3390/molecules30234633
Primary Topic
Receptor Mechanisms and Signaling
Type
article
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article

SERAAK2 as a Serotonin Receptor Ligand: Structural and Pharmacological In Vitro and In Vivo Evaluation

Marián Castro, Ewa Kędzierska, Michał K. Jastrzębski, Katarzyna Szczepańska et al.
Molecules
Receptor Mechanisms and Signaling
article

SERAAK2 as a Serotonin Receptor Ligand: Structural and Pharmacological In Vitro and In Vivo Evaluation

Marián Castro, Ewa Kędzierska, Michał K. Jastrzębski, Katarzyna Szczepańska, Tadeusz P. Karcz, Agnieszka A. Kaczor, Agata Zięba, Tuomo Laitinen
article en

Abstract

Serotonin receptors, in particular 5-HT<sub>1A</sub> and 5-HT<sub>2A</sub> receptors, are important molecular targets for the central nervous system (CNS) disorders, such as schizophrenia, depression, anxiety disorders, memory deficits, and many others. Here, we present structural and pharmacological evaluation of a serotonin receptor ligand, SERAAK2, identified in a structure-based virtual screening campaign. Molecular docking studies revealed that SERAAK2 binds with its molecular targets via Asp3.32 as the main anchoring point, which is typical for orthosteric ligands of aminergic GPCRs. Molecular dynamics simulations confirmed the stability of the ligand binding poses in the studied receptors. MMGBSA calculations were in accordance with the receptor in vitro binding affinity studies, which indicated that SERAAK2 is a potent ligand of 5-HT<sub>1A</sub> and 5-HT<sub>2A</sub> receptors. It was also found that SERAAK2 displays favorable ADMET parameters. The demonstrated anxiolytic- and antidepressant-like effects of SERAAK2 in animal models, which may involve its interaction with 5-HT<sub>1A</sub> receptors, warrant further studies to confirm these activities and elucidate the underlying mechanisms.

MoleculesVol. 30(23)
Medical University of Lublin (PL), Jagiellonian University (PL), University of Eastern Finland (FI), Center for Research in Molecular Medicine and Chronic Diseases (ES), Maj Institute of Pharmacology (PL), Instituto de Investigación Sanitaria de Santiago (ES)
Openalex Percentile: Top 66%
Receptor Mechanisms and Signaling
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