Azole antifungal compounds could have dual cholinesterase inhibitory potential according to virtual screening, enzyme kinetics, and toxicity studies of an inhouse library

BARUT B., SARI S., SABUNCUOĞLU S., ÖZEL A.

Journal of Molecular Structure, cilt.1235, 2021 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 1235
  • Basım Tarihi: 2021
  • Doi Numarası: 10.1016/j.molstruc.2021.130268
  • Dergi Adı: Journal of Molecular Structure
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Chemical Abstracts Core, INSPEC
  • Anahtar Kelimeler: Azole antifungal, Virtual screening, Acetylcholinesterase, Butyrylcholinesterase, Enzyme kinetics, Molecular docking, Cytotoxicity, HUMAN ACETYLCHOLINESTERASE, ALZHEIMERS, BUTYRYLCHOLINESTERASE, DERIVATIVES, DISCOVERY, DISEASE, COMPLEX, PROTEIN, DRUGS
  • Karadeniz Teknik Üniversitesi Adresli: Evet

Özet

© 2021Recent advances in cholinesterase inhibitors opened new venues for the treatment of cognitive disorders like Alzheimer's disease. Certain azole antifungals like miconazole were reported to have cholinesterase inhibitory effects and hence ameliorate cognitive deficits. In this study, we tested a set of azole antifungal derivatives selected through virtual screening of an inhouse library for their acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitory effects. Compound 61 showed potent and selective AChE inhibition (IC50 = 8.77 µM). The study also yielded dual AChE/BChE inhibitors in addition to a number of potent AChE inhibitors. Enzyme kinetics assays revealed that AChE inhibitors were competitive inhibitors. All the active compounds were imidazole derivatives and the modeling study showed that imidazole at protonated state contributed greatly to the binding interactions with some key residues of AChE and BChE active site. The active derivatives had negligible cytotoxic effects on murine fibroblast viability. According to our results, compounds featuring the classical scaffold of azole antifungal drugs could hold high potential for anticholinesterase drug design.