Gregor_1992_Bioorg.Med.Chem.Letters_2_861

Reference

Title : The synthesis and in vitro acetylcholinesterase and butyrylcholinesterase inhibitory activity of tacrine (Cognex) derivaties - Gregor_1992_Bioorg.Med.Chem.Letters_2_861
Author(s) : Gregor VE , Emmerling MR , Lee C , Moore CJ
Ref : Bioorganic & Medicinal Chemistry Letters , 2 :861 , 1992
Abstract :

Chlorosubstituted derivatives of tacrine (1), 1,4-methylenetacrine (2), and their in vitro acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitory activities are described. The most potent analogues are 6-chlorotacrine (1b) in AChE and 7-chlorotacrine (1c) in BChE inhibition.

PubMedSearch : Gregor_1992_Bioorg.Med.Chem.Letters_2_861
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Related information

Inhibitor 6-chlorotacrine

Citations formats

Gregor VE, Emmerling MR, Lee C, Moore CJ (1992)
The synthesis and in vitro acetylcholinesterase and butyrylcholinesterase inhibitory activity of tacrine (Cognex) derivaties
Bioorganic & Medicinal Chemistry Letters 2 :861

Gregor VE, Emmerling MR, Lee C, Moore CJ (1992)
Bioorganic & Medicinal Chemistry Letters 2 :861