Cholinesterase Inhibition Activity and Docking Simulation Study of Coumarin Mannich Base Derivatives
Inhibition of acetylcholinesterase and butyrylcholinesterase (AChE and BuChE) as two major forms of cholinesterases (ChEs) is considered as the common approach for the treatment of Alzheimer's disease (AD). The present study was done to explore the anticholinesterase inhibition property of coum...
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University of Tehran
2019-01-01
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| Series: | Journal of Sciences, Islamic Republic of Iran |
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| Online Access: | https://jsciences.ut.ac.ir/article_69627_5849f8f2f225aebc917e6b922c874ea0.pdf |
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| author | Ali Kiani Leili Jalili-baleh Zahra Abdollahi Hamid Nadri Alireza Foroumadi Seyed Esmaeil Sadat Ebrahimi Mehdi Khoobi |
| author_facet | Ali Kiani Leili Jalili-baleh Zahra Abdollahi Hamid Nadri Alireza Foroumadi Seyed Esmaeil Sadat Ebrahimi Mehdi Khoobi |
| author_sort | Ali Kiani |
| collection | DOAJ |
| description | Inhibition of acetylcholinesterase and butyrylcholinesterase (AChE and BuChE) as two major forms of cholinesterases (ChEs) is considered as the common approach for the treatment of Alzheimer's disease (AD). The present study was done to explore the anticholinesterase inhibition property of coumarin Mannich base derivatives. A series of cumarin Manich bases were synthesized (4a-h) through one-pot tri-component reaction in an environmentally friendly condition and evaluated against AChE and BuChE by Ellman's assay. Ligand-protein docking simulation was also performed for the most active compound 4a. Additionally, the criteria of drug likeness of the target compounds was predicted using SwissADME web service. All compounds exhibited weak to moderate inhibitory activity against both AChE and BuChE enzymes. Compound 4a containing p-tolyl piperazin group showed the best activity against AChE (42.4 % at 32 µM), while compound 4g bearing phenylpiperazine moiety was the best BuChE inhibitor (43.9% at 32 µM). Ligand-protein docking simulation also exhibited that the main part of compound 4a in ChE inhibitory activity is amine moiety. Moreover, the prediction of "Lipinski's rule of five" showed that most target compounds can cross the BBB and have properties that would make them likely orally active compounds in humans. This study suggested that the synthesized cumarin Manich bases with some more structural modifications may be considered as a potential compound to target AChE and BuChE. |
| format | Article |
| id | doaj-art-48141ab3ca0d4cb48b8eb24beb4c888d |
| institution | OA Journals |
| issn | 1016-1104 2345-6914 |
| language | English |
| publishDate | 2019-01-01 |
| publisher | University of Tehran |
| record_format | Article |
| series | Journal of Sciences, Islamic Republic of Iran |
| spelling | doaj-art-48141ab3ca0d4cb48b8eb24beb4c888d2025-08-20T02:25:54ZengUniversity of TehranJournal of Sciences, Islamic Republic of Iran1016-11042345-69142019-01-0130151210.22059/jsciences.2019.256053.100724769627Cholinesterase Inhibition Activity and Docking Simulation Study of Coumarin Mannich Base DerivativesAli Kiani0Leili Jalili-baleh1Zahra Abdollahi2Hamid Nadri3Alireza Foroumadi4Seyed Esmaeil Sadat Ebrahimi5Mehdi Khoobi6Department of medical Chemistry, school of pharmacy, International campus, Tehran University of Medical Science (IC-TUMS),Tehran, Iran.The Institute of Pharmaceutical Sciences (TIPS), Tehran University of Medical Sciences, Tehran 1417614411, IranDepartment of Medicinal Chemistry, Faculty of pharmacy and Pharmaceutical sciences research center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.Department of Medicinal Chemistry, Faculty of pharmacy and Pharmaceutical sciences research center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.Tehran University of Medical SciencesDepartment of Medicinal Chemistry, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran, IranInhibition of acetylcholinesterase and butyrylcholinesterase (AChE and BuChE) as two major forms of cholinesterases (ChEs) is considered as the common approach for the treatment of Alzheimer's disease (AD). The present study was done to explore the anticholinesterase inhibition property of coumarin Mannich base derivatives. A series of cumarin Manich bases were synthesized (4a-h) through one-pot tri-component reaction in an environmentally friendly condition and evaluated against AChE and BuChE by Ellman's assay. Ligand-protein docking simulation was also performed for the most active compound 4a. Additionally, the criteria of drug likeness of the target compounds was predicted using SwissADME web service. All compounds exhibited weak to moderate inhibitory activity against both AChE and BuChE enzymes. Compound 4a containing p-tolyl piperazin group showed the best activity against AChE (42.4 % at 32 µM), while compound 4g bearing phenylpiperazine moiety was the best BuChE inhibitor (43.9% at 32 µM). Ligand-protein docking simulation also exhibited that the main part of compound 4a in ChE inhibitory activity is amine moiety. Moreover, the prediction of "Lipinski's rule of five" showed that most target compounds can cross the BBB and have properties that would make them likely orally active compounds in humans. This study suggested that the synthesized cumarin Manich bases with some more structural modifications may be considered as a potential compound to target AChE and BuChE.https://jsciences.ut.ac.ir/article_69627_5849f8f2f225aebc917e6b922c874ea0.pdfalzheimer’s diseaseacetylcholinesterasebutyrylcholinesterse4-hydroxycoumarinmannich base |
| spellingShingle | Ali Kiani Leili Jalili-baleh Zahra Abdollahi Hamid Nadri Alireza Foroumadi Seyed Esmaeil Sadat Ebrahimi Mehdi Khoobi Cholinesterase Inhibition Activity and Docking Simulation Study of Coumarin Mannich Base Derivatives Journal of Sciences, Islamic Republic of Iran alzheimer’s disease acetylcholinesterase butyrylcholinesterse 4-hydroxycoumarin mannich base |
| title | Cholinesterase Inhibition Activity and Docking Simulation Study of Coumarin Mannich Base Derivatives |
| title_full | Cholinesterase Inhibition Activity and Docking Simulation Study of Coumarin Mannich Base Derivatives |
| title_fullStr | Cholinesterase Inhibition Activity and Docking Simulation Study of Coumarin Mannich Base Derivatives |
| title_full_unstemmed | Cholinesterase Inhibition Activity and Docking Simulation Study of Coumarin Mannich Base Derivatives |
| title_short | Cholinesterase Inhibition Activity and Docking Simulation Study of Coumarin Mannich Base Derivatives |
| title_sort | cholinesterase inhibition activity and docking simulation study of coumarin mannich base derivatives |
| topic | alzheimer’s disease acetylcholinesterase butyrylcholinesterse 4-hydroxycoumarin mannich base |
| url | https://jsciences.ut.ac.ir/article_69627_5849f8f2f225aebc917e6b922c874ea0.pdf |
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