Tytuł pozycji:
Multifunctional Arylsulfone and Arylsulfonamide-Based Ligands with Prominent Mood-Modulating Activity and Benign Safety Profile, Targeting Neuropsychiatric Symptoms of Dementia
- Tytuł:
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Multifunctional Arylsulfone and Arylsulfonamide-Based Ligands with Prominent Mood-Modulating Activity and Benign Safety Profile, Targeting Neuropsychiatric Symptoms of Dementia
- Autorzy:
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Wesołowska, Anna
Abram, Michał
Kołaczkowski, Marcin
Bucki, Adam
Kotańska, Magdalena
Żmudzki, Paweł
Mierzejewski, Paweł
Marcinkowska, Monika
Wyska, Elżbieta
Mika, Kamil
Cios, Agnieszka
Siwek, Agata
Głuch-Lutwin, Monika
Partyka, Anna
Śniecikowska, Joanna
Przejczowska-Pomierny, Katarzyna
Zagórska, Agnieszka
Fajkis-Zajączkowska, Nikola
Jastrzębska-Więsek, Magdalena
- Data publikacji:
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2021
- Język:
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angielski
- ISBN, ISSN:
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00222623
- Prawa:
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Udzielam licencji. Uznanie autorstwa 4.0 Międzynarodowa
http://creativecommons.org/licenses/by/4.0/legalcode.pl
- Linki:
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https://pubs.acs.org/doi/10.1021/acs.jmedchem.1c00497  Link otwiera się w nowym oknie
- Dostawca treści:
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Repozytorium Uniwersytetu Jagiellońskiego
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The current pharmaceutical market lacks therapeutic agents designed to modulate behavioral disturbances associated with dementia. To address this unmet medical need, we designed multifunctional ligands characterized by a nanomolar affinity for clinically relevant targets that are associated with the disease pathology, namely, the 5-HT2A/6/7 and D2 receptors. Compounds that exhibited favorable functional efficacy, water solubility, and metabolic stability were selected for more detailed study. Pharmacological profiling revealed that compound 11 exerted pronounced antidepressant activity (MED 0.1 mg/kg), outperforming commonly available antidepressant drugs, while compound 16 elicited a robust anxiolytic activity (MED 1 mg/kg), exceeding comparator anxiolytics. In contrast to the existing psychotropic agents tested, the novel chemotypes did not negatively impact cognition. At a chronic dose regimen (25 days), 11 did not induce significant metabolic or adverse blood pressure disturbances. These promising therapeutic-like activities and benign safety profiles make the novel chemotypes potential treatment options for dementia patients.