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Design, synthesis and evaluation of pyrimidine derivatives as sedative-hypnotic agents.
- Source :
-
European journal of medicinal chemistry [Eur J Med Chem] 2025 Feb 15; Vol. 284, pp. 117213. Date of Electronic Publication: 2024 Dec 27. - Publication Year :
- 2025
-
Abstract
- Insomnia is a mental disorder in which drugs only alleviate the symptoms but also produce adverse effects. Therefore, developing innovative sedative-hypnotic agents is urgent. In this work, twenty-five novel heteroatomic compounds were designed, synthesized, and screened for their sedative activities, structurally featuring the fusion of pyrimidine and carbazole or benzothiazole. Most of the synthesized compounds showed distinct sedative activities in vivo. Among them, 4l displayed excellent sedative and hypnotic properties in the dose range of 0.1-2.5 mg/kg, and was superior to diazepam at 5 mg/kg. Mechanism studies showed 4l induced sedative-hypnotic effects via activating cAMP/PKA/CREB signaling pathway. Moreover, 4l possessed appropriate blood brain barrier permeability and excellent bioavailability (F: 74.5 ± 4.5 %). Thus, 4l was identified as the lead compound owing to its favorable potency and pharmacokinetic profiles, providing alternative for insomnia drugs development.<br />Competing Interests: Declaration of competing interest The authors declare that they have no competing interest.<br /> (Copyright © 2024 Elsevier Masson SAS. All rights reserved.)
- Subjects :
- Animals
Mice
Structure-Activity Relationship
Molecular Structure
Dose-Response Relationship, Drug
Male
Blood-Brain Barrier metabolism
Pyrimidines chemistry
Pyrimidines pharmacology
Pyrimidines chemical synthesis
Hypnotics and Sedatives pharmacology
Hypnotics and Sedatives chemistry
Hypnotics and Sedatives chemical synthesis
Drug Design
Subjects
Details
- Language :
- English
- ISSN :
- 1768-3254
- Volume :
- 284
- Database :
- MEDLINE
- Journal :
- European journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 39742697
- Full Text :
- https://doi.org/10.1016/j.ejmech.2024.117213