Identification of butyrylcholinesterase and monoamine oxidase B targeted ligands and their putative application in Alzheimer's treatment: A computational strategy

• Published in: Current pharmaceutical design
• Main Authors: Jabir, Nasimudeen R, Rehman, Md Tabish, Tabrez, Shams, Alserihi, Raed F, AlAjmi, Mohamed F, Khan, Mohd Shahnawaz, Husain, Fohad Mabood, Ahmed, Bakrudeen Ali
• Format: Journal Article
• Language: English
• Published: United Arab Emirates 01.01.2021
• Subjects: Monoamine oxidase B; Monoamine oxidase A; Molecular docking and simulation; Multi-targeted ligands; Drug development; Alzheimer's disease; Butylrylcholinesterase
• ISSN: 1873-4286
• DOI: 10.2174/1381612827666210226123240

With the burgeoning worldwide aging population, the incidence of Alzheimer's disease (AD) and its associated disorders is continuously rising. To appraise other relevant drug targets that could lead to potent enzyme targeting, 13 previously predicted ligands (shown favorable binding with AChE (acetylcholinesterase) and GSK-3 (glycogen synthase kinase) were screened for targeting 3 different enzymes namely butyrylcholinesterase (BChE), monoamine oxidase A (MAO-A), and monoamine oxidase B (MAO-B) to possibly meet the unmet medical need of better AD treatment. The study utilized in silico screening of 13 ligands against BChE, MAO-A and MAO-B using PyRx-Python prescription 0.8. The visualization of active interaction of studied compounds with targeted proteins was performed by Discovery Studio 2020 (BIOVIA). The computational screening of studied ligands revealed the docking energies in the range of -2.4 to -11.3 kcal/mol for all the studied enzymes. Among the 13 ligands, 8 ligands (55E, 6Z2, 6Z5, BRW, F1B, GVP, IQ6, and X37) showed the binding energies of ≤ -8.0 kcal/mol towards BChE, MAO-A and MAO-B. The ligand 6Z5 was found to be the most potent inhibitor of BChE and MAO-B, with a binding energy of -9.7 and -10.4 kcal mol respectively. Molecular dynamics simulation of BChE-6Z5 and MAO-B-6Z5 complex confirmed the formation of a stable complex. Our computational screening, molecular docking, and molecular dynamics simulation studies revealed that the above-mentioned enzymes targeted ligands might expedite the future design of potent anti-AD drugs generated on this chemical scaffold.