| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 7801896 | European Journal of Medicinal Chemistry | 2013 | 47 Pages |
Abstract
A novel series of hybrid structures, composed of two known scaffolds including tetrahydroaminoquinoline and coumarin were synthesized and evaluated for both acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) inhibitory activities.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Mehdi Khoobi, Masoumeh Alipour, Alireza Moradi, Amirhossein Sakhteman, Hamid Nadri, Seyyede Faeze Razavi, Mehdi Ghandi, Alireza Foroumadi, Abbas Shafiee,
![First Page Preview: Design, synthesis, docking study and biological evaluation of some novel tetrahydrochromeno [3â²,4â²:5,6]pyrano[2,3-b]quinolin-6(7H)-one derivatives against acetyl- and butyrylcholinesterase Design, synthesis, docking study and biological evaluation of some novel tetrahydrochromeno [3â²,4â²:5,6]pyrano[2,3-b]quinolin-6(7H)-one derivatives against acetyl- and butyrylcholinesterase](/preview/png/7801896.png)