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  2. Multitarget-directed carbamate and carbamothioate derivatives: Cholinesterase and monoamine oxidase inhibition, anti-β-amyloid (Aβ) aggregation, antioxidant and blood-brain barrier permeation properties against Alzheimer's disease

Multitarget-directed carbamate and carbamothioate derivatives: Cholinesterase and monoamine oxidase inhibition, anti-β-amyloid (Aβ) aggregation, antioxidant and blood-brain barrier permeation properties against Alzheimer's disease

  • Eur J Med Chem. 2025 Nov 15:298:117986. doi: 10.1016/j.ejmech.2025.117986.
Senel Teke Tuncel 1 Sule Erol Gunal 2 İlke Demir 3 İpek Baysal 4 Safiye Sag Erdem 3 Gökçen Telli 5 Gulberk Ucar 6 Ilknur Dogan 7 Nesrin Gokhan Kelekci 8
Affiliations

Affiliations

  • 1 Bogazici University, Department of Chemistry, Bebek, 34342, Istanbul, Turkey; İstanbul Arel University, Department of Molecular Biology and Genetics, 34537, Istanbul, Turkey.
  • 2 İstanbul University-Cerrahpaşa, Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Istanbul, Turkey.
  • 3 Marmara University, Department of Chemistry, Faculty of Science, Göztepe, Istanbul, 34722, Turkey.
  • 4 Hacettepe University, Graduate School of Health Sciences, Department of One Health, Ankara, Turkey; Hacettepe University, Vocational School of Health Services, Ankara, Turkey.
  • 5 Hacettepe University, Faculty of Pharmacy, Department of Pharmacology, Sıhhiye, Ankara, 06100, Turkey.
  • 6 Hacettepe University, Faculty of Pharmacy, Department of Biochemistry, Sıhhiye, Ankara, 06100, Turkey.
  • 7 Bogazici University, Department of Chemistry, Bebek, 34342, Istanbul, Turkey.
  • 8 Hacettepe University, Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Sıhhiye, Ankara, 06100, Turkey. Electronic address: onesrin@hacettepe.edu.tr.
Abstract

Neurodegenerative diseases are multifactorial disorders characterized by protein misfolding, oxidative stress, and neuroinflammation, finally resulting in neuronal loss and cognitive dysfunctions. Nowadays, an attractive strategy to improve the classical treatments is the development of multitarget-directed molecules able to synergistically interact with different Enzymes and/or receptors. A novel series of chiral carbamate and carbamothioate derivatives were designed, synthesized, and investigated as inhibition of cholinesterases and monoamine oxidases, anti-β-amyloid aggregation and antioxidant activities against Alzheimer's disease. The enzymatic activity of butyrylcholinesterase (BChE) in the brain increases with the progression of Alzheimer's disease, thus classifying BChE as a promising drug target in advanced Alzheimer's disease. Two compounds, 4a-S and 4a-R, showed excellent and selective inhibitory activities against BChE (IC50: 0.051 μM; IC50: 0.059 μM). Compound 4a-S also exhibited selective hMAO-B (IC50 = 0.45 ± 0.02 μM) inhibitory activities. The molecular docking and dynamic simulations of compounds 4a-R and 4a-S in human BChE revealed that the piperidine and propargyl groups play crucial roles for the inhibition. Compound 1d-R had the greatest ability to hMAO-B inhibition (IC50 = 0.09 μM). Compound 2b exhibited significant ability to inhibit self-induced β-amyloid (Aβ1-42; IC50: 0.97 μM). Achiral carbamate derivatives 2c, 2j and 2a act as potential Antioxidants. Among the compounds, 2c, 2i, 2j, 4a-S were selected for the PAMPA-BBB test. These compounds demonstrated excellent penetration into the central nervous system. Compounds 1d-R, 2b, 2c, 4a-S and 4a-R were assessed in vivo with Aluminium chloride induced Alzheimer mice model. Compounds 1d-R, 2b, and 4a-S increased learning according to Morris Water Maze test. Our preliminary findings may open-up the way for developing innovative carbamate and carbamothioate derivatives against neurodegenerative diseases.

Keywords

Alzheimer's disease; Anti-β-Amyloid; Carbamate; Carbamothioate; MTDL; Morris water maze test; PAMPA; hBChE; hMAO-B.

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