Jia_2009_Eur.J.Med.Chem_44_772

Reference

Title : Design, synthesis and evaluation of galanthamine derivatives as acetylcholinesterase inhibitors - Jia_2009_Eur.J.Med.Chem_44_772
Author(s) : Jia P , Sheng R , Zhang J , Fang L , He Q , Yang B , Hu Y
Ref : Eur Journal of Medicinal Chemistry , 44 :772 , 2009
Abstract :

A new series of galanthamine derivatives have been designed, synthesized and evaluated as acetylcholinesterase inhibitors. All of the new compounds prepared showed high AChE inhibitory activities, with compound 3e that has an N-hexyl-benzyl piperidine substituent on the nitrogen atom reaching the best inhibitory activity for AChE (IC(50)=5.62 nM). The docking study performed with AutoDock demonstrated that 3e was nicely accommodated by AChE.

PubMedSearch : Jia_2009_Eur.J.Med.Chem_44_772
PubMedID: 18550228

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Citations formats

Jia P, Sheng R, Zhang J, Fang L, He Q, Yang B, Hu Y (2009)
Design, synthesis and evaluation of galanthamine derivatives as acetylcholinesterase inhibitors
Eur Journal of Medicinal Chemistry 44 :772

Jia P, Sheng R, Zhang J, Fang L, He Q, Yang B, Hu Y (2009)
Eur Journal of Medicinal Chemistry 44 :772