Design, Synthesis and Characterization of Novel Urolithin Derivatives as Cholinesterase Inhibitor Agents

Author(s): Maryam Norouzbahari , Emine V. Burgaz , Tugba Ercetin , Amirhossein Fallah , Alireza Foroumadi , Loghman Firoozpour , Mustafa F. Sahin , Mustafa Gazi , Hayrettin O. Gulcan* .

Journal Name: Letters in Drug Design & Discovery

Volume 15 , Issue 11 , 2018

Become EABM
Become Reviewer

Graphical Abstract:


Abstract:

Background: Considering the limitations of current cholinesterase inhibitor drugs for the treatment of Alzheimer’s disease, there is ongoing research activities to find out alternative drug candidates. The aryl-spacer-N-benzyl pharmacophore model has been effectively utilized to design various types of cholinesterase inhibitor molecules, including donepezil. Within this research study, we have questioned the significance of the benzyl group within this pharmacophore employing the urolithin derivatives. Urolithins are benzo[c]chromene analogue metabolites of ellagitannins, abundantly found in pomegranate and berry fruits.

Methods: Employing the previous experience that urolithin-spacer-N-benzyl yielded out potent cholinesterase inhibitors, we have designed novel benzo[c]chromene derivatives either lacking the benzyl group or possessing benzyl group in isoquinoline moiety lacking free N-C bond rotation. Following the synthesis and structure identification studies the compounds were screened for their potential to inhibit cholinesterase enzymes. Furthermore, the title compounds were also evaluated for their potential to prevent cholinesterase-accelerated amyloid beta aggregation. In the final, the most active compound was examined to find out its interactions with the cholinesterase enzyme employing a molecular docking study.

Results: The title compounds displayed varying cholinesterase inhibitory potential. Some of the compounds were found more / comparable activity to the activity of the current drugs employed in clinic. The potential of the title molecules to inhibit amyloid beta aggregation was found poor.

Conclusion: The title compounds displayed varying cholinesterase inhibitory potential, implying that the benzyl group is not a must in each design. This was also shown with the molecular docking studies. On the other hand, the beta amyloid aggregation studies have pointed out that cholinesterase inhibition does not guarantee the prevention of cholinesterase-accelerated amyloid beta aggregation.

Keywords: Alzheimer`s disease, acetylcholinesterase, butyrylcholinesterase, urolithin, donepezil, drugs.

Rights & PermissionsPrintExport Cite as

Article Details

VOLUME: 15
ISSUE: 11
Year: 2018
Page: [1131 - 1140]
Pages: 10
DOI: 10.2174/1570180815666180115144608
Price: $58

Article Metrics

PDF: 26
HTML: 3
EPUB: 1