Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/55915
Title: Synthesis and evaluation of 2,3,4,9-tetrahydro-1H-carbazole derivatives as selective acetylcholinesterase inhibitors: Potential anti-Alzheimer’s agents
Authors: Kukreja, Hitesh
Chugh, Rajan
Singh, Jatinder
Shah, Ramanpreet
Singh, Dhandeep
Singh, Nirmal
Chopra, Dimple Sethi
Singh, Mandeep
Keywords: Alzheimer’s disease;Acetylcholinesterase (AChE);Borsche-Drechsel cyclization reaction;Donepzil;2,3,4,9-tetrahydro-1H-carbazoles
Issue Date: Jan-2021
Publisher: NISCAIR-CSIR, India
Abstract: Alzheimer’s disease is an irreversible, progressive brain disorder that slowly destroys memory and cognition skills. Dysfunction of acetylcholine containing neurons in the brain contributes substantially to the cognitive decline observed in Alzheimer's disease. Hence, our focus is to synthesize cholinesterase inhibitors. A series (22 compounds) of 6- and 9-substituted derivatives of 2,3,4,9-tetrahydro-1H-carbazole have been prepared and in vitro evaluated for acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibition by Ellman’s method. By comparing selectivity with standard drug donepezil, amino derivative 3, methylamino derivative 4 and butyl nitro derivative 17 have been found to be selective AChE inhibitors. Borsche-Drechsel cyclization reaction has been carried out to synthesize 2,3,4,9-tetrahydrocarbazole ring followed by nitration, reduction and derivative synthesis.
Page(s): 152-160
URI: http://nopr.niscair.res.in/handle/123456789/55915
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.60B(01) [January 2021]

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