| Literature DB >> 28279561 |
Ammar Maryamabadi1, Alireza Hasaninejad2, Najmeh Nowrouzi1, Gholamhossein Mohebbi3.
Abstract
A convenient synthesis of substituted spiroindenoquinoxalines at mild and green conditions was developed. Multicomponent reaction of substituted phenylene diamines, ninhydrin, malononitrile and N,N'-substituted-2-nitroethene-1,1-diamines produced the target compounds. Twelve new spiroindenoquinoxalines were obtained, and their ability in inhibition of acetyl and butyrylcholinesterases were investigated both in vitro and in silico. All compounds showed moderate level activity against both acetyl and butyrylcholinesterases.Entities:
Keywords: Acetylcholinesterase inhibition; Butyrylcholinesterase inhibition; Catalyst-free; Indenoquinoxaline; Multi-component reactions
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Year: 2017 PMID: 28279561 DOI: 10.1016/j.bmc.2017.02.017
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641