Design, Synthesis, and Evaluation of Novel 2 H-Benzo[b][1,4]thiazin-3(4 H)-one Derivatives as New Acetylcholinesterase Inhibitors

Molecules. 2022 Mar 25;27(7):2121. doi: 10.3390/molecules27072121.

Abstract

Alzheimer's disease (AD) is a slowly progressive neurodegenerative disease that causes dementia in people aged 65 and over. In the present study, a series of thiadiazole hybrid compounds with benzothiazine derivatives as acetylcholinesterase inhibitors were developed and evaluated for their biological activity. The AChE and BChE inhibition potentials of all compounds were evaluated by using the in vitro Ellman method. The biological evaluation showed that compounds 3i and 3j displayed significant inhibitory activity against AChE. Compounds 3i and 3j showed IC50 values of 0.027 µM and 0.025 µM against AChE, respectively. The reference drug donepezil (IC50 = 0.021 µM) also showed significant inhibition against AChE. Further docking simulation also revealed that these compounds (3i and 3j) interacted with the active site of the enzyme similarly to donepezil. The antioxidant study revealed that compounds 3i and 3j exhibited greater antioxidant effects. An in vitro blood-brain barrier permeability study showed that compounds 3i and 3j are promising compounds against AD. The cytotoxicity study of compounds 3i and 3j showed non-cytotoxic with an IC50 value of 98.29 ± 3.98 µM and 159.68 ± 5.53 µM against NIH/3T3 cells, respectively.

Keywords: Alzheimer’s disease; acetylcholinesterase; antioxidant activity; benzothiazine; blood–brain barrier permeability; cytotoxicity; molecular docking; thiadiazole.

MeSH terms

  • Acetylcholinesterase / metabolism
  • Alzheimer Disease* / drug therapy
  • Animals
  • Antioxidants / chemistry
  • Antioxidants / pharmacology
  • Cholinesterase Inhibitors / chemistry
  • Donepezil / pharmacology
  • Drug Design
  • Humans
  • Mice
  • Molecular Docking Simulation
  • Neurodegenerative Diseases*
  • Structure-Activity Relationship

Substances

  • Antioxidants
  • Cholinesterase Inhibitors
  • Donepezil
  • Acetylcholinesterase