(2017) Synthesis, docking study and neuroprotective effects of some novel pyrano 3,2-<i>c</i> chromene derivatives bearing morpholine/phenylpiperazine moiety. Bioorganic & medicinal chemistry. pp. 3980-3988. ISSN 0968-0896
Full text not available from this repository.
Abstract
Novel pyrano3,2-cchromene derivatives bearing morpholine/phenylpiperazine moiety were synthesized and evaluated against acetylcholinestrase (AChE) and butylcholinestrase (BuChE). Among the synthesized compounds, N-(3-cyano-4-(4-methoxyphenyl)-5-oxo-4,5-dihydropyrano3,2-cchromen-2-yl)-2-(4-phenylpiperazin-1-yl)acetamide (6c) exhibited the highest acetylcholinestrase inhibitory (AChEI) activity (IC50 = 1.12 mu M) and most of them showed moderate butylcholinestrase inhibitory activity (BChEI). Kinetic study of compound 6c confirmed mixed type of inhibition towards AChE which was in covenant with the results obtained from docking study. Also, it was evaluated against beta-secretase which demonstrated low activity (inhibition percentage: 18%). It should be noted that compounds 6c, 7b, 6g, and 7d showed significant neuroprotective effects against H2O2-induced PC12 oxidative stress. (C) 2017 Elsevier Ltd. All rights reserved.
Item Type: | Article |
---|---|
Keywords: | Alzheimer's disease Cholinesterase inhibition Coumarins Neuroprotection beta-Secretase inhibition alzheimers-disease acetylcholinesterase inhibitors amyloid-beta coumarins design Biochemistry & Molecular Biology Pharmacology & Pharmacy Chemistry |
Page Range: | pp. 3980-3988 |
Journal or Publication Title: | Bioorganic & medicinal chemistry |
Journal Index: | WoS |
Volume: | 25 |
Number: | 15 |
Identification Number: | https://doi.org/10.1016/j.bmc.2017.05.043 |
ISSN: | 0968-0896 |
Depositing User: | Mr mahdi sharifi |
URI: | http://eprints.ssu.ac.ir/id/eprint/30313 |
Actions (login required)
![]() |
View Item |