Synthesis, biological evaluation and molecular modelling of 2′-hydroxychalcones as acetylcholinesterase inhibitors
A series of 2′-hydroxy- and 2′-hydroxy-4′,6′-dimethoxychalcones was synthesised and evaluated as inhibitors of human acetylcholinesterase (AChE). The majority of the compounds were found to show some activity, with the most active compounds having IC50 values of 40-85 μM. Higher activities were gene...
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my.uniten.dspace-35002020-06-29T04:13:48Z Synthesis, biological evaluation and molecular modelling of 2′-hydroxychalcones as acetylcholinesterase inhibitors Sukumaran, S.D. Chee, C.F. Viswanathan, G. Buckle, M.J.C. Othman, R. Rahman, N.A. Chung, L.Y. A series of 2′-hydroxy- and 2′-hydroxy-4′,6′-dimethoxychalcones was synthesised and evaluated as inhibitors of human acetylcholinesterase (AChE). The majority of the compounds were found to show some activity, with the most active compounds having IC50 values of 40-85 μM. Higher activities were generally observed for compounds with methoxy substituents in the A ring and halogen substituents in the B ring. Kinetic studies on the most active compounds showed that they act as mixed-type inhibitors, in agreement with the results of molecular modelling studies, which suggested that they interact with residues in the peripheral anionic site and the gorge region of AChE. © 2016 by the authors; licensee MDPI. 2017-10-27T06:14:23Z 2017-10-27T06:14:23Z 2016 Article 10.3390/molecules21070955 en Molecules Volume 21, Issue 7, 2016, Article number 955 |
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A series of 2′-hydroxy- and 2′-hydroxy-4′,6′-dimethoxychalcones was synthesised and evaluated as inhibitors of human acetylcholinesterase (AChE). The majority of the compounds were found to show some activity, with the most active compounds having IC50 values of 40-85 μM. Higher activities were generally observed for compounds with methoxy substituents in the A ring and halogen substituents in the B ring. Kinetic studies on the most active compounds showed that they act as mixed-type inhibitors, in agreement with the results of molecular modelling studies, which suggested that they interact with residues in the peripheral anionic site and the gorge region of AChE. © 2016 by the authors; licensee MDPI. |
| format |
Article |
| author |
Sukumaran, S.D. Chee, C.F. Viswanathan, G. Buckle, M.J.C. Othman, R. Rahman, N.A. Chung, L.Y. |
| spellingShingle |
Sukumaran, S.D. Chee, C.F. Viswanathan, G. Buckle, M.J.C. Othman, R. Rahman, N.A. Chung, L.Y. Synthesis, biological evaluation and molecular modelling of 2′-hydroxychalcones as acetylcholinesterase inhibitors |
| author_facet |
Sukumaran, S.D. Chee, C.F. Viswanathan, G. Buckle, M.J.C. Othman, R. Rahman, N.A. Chung, L.Y. |
| author_sort |
Sukumaran, S.D. |
| title |
Synthesis, biological evaluation and molecular modelling of 2′-hydroxychalcones as acetylcholinesterase inhibitors |
| title_short |
Synthesis, biological evaluation and molecular modelling of 2′-hydroxychalcones as acetylcholinesterase inhibitors |
| title_full |
Synthesis, biological evaluation and molecular modelling of 2′-hydroxychalcones as acetylcholinesterase inhibitors |
| title_fullStr |
Synthesis, biological evaluation and molecular modelling of 2′-hydroxychalcones as acetylcholinesterase inhibitors |
| title_full_unstemmed |
Synthesis, biological evaluation and molecular modelling of 2′-hydroxychalcones as acetylcholinesterase inhibitors |
| title_sort |
synthesis, biological evaluation and molecular modelling of 2′-hydroxychalcones as acetylcholinesterase inhibitors |
| publishDate |
2017 |
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1671342875113160704 |
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13.223943 |