Pan_2008_Bioorg.Med.Chem.Lett_18_3790

Reference

Title : Design, synthesis and evaluation of isaindigotone derivatives as acetylcholinesterase and butyrylcholinesterase inhibitors - Pan_2008_Bioorg.Med.Chem.Lett_18_3790
Author(s) : Pan L , Tan JH , Hou JQ , Huang SL , Gu LQ , Huang ZS
Ref : Bioorganic & Medicinal Chemistry Lett , 18 :3790 , 2008
Abstract :

A series of isaindigotone derivatives 5a-d and 6a-d were designed, synthesized and evaluated as acetylcholinesterase and butyrylcholinesterase inhibitors. Results showed that the novel class of isaindigotone derivatives could inhibit both cholinesterases and the selectivity of AChE over BuChE inhibition was related to the aromatic, the species and length of the alkyl amino side chain of compounds. The structure-activity relationships were discussed and their multiple binding modes were further clarified in the molecular docking studies.

PubMedSearch : Pan_2008_Bioorg.Med.Chem.Lett_18_3790
PubMedID: 18524585

Related information

Citations formats

Pan L, Tan JH, Hou JQ, Huang SL, Gu LQ, Huang ZS (2008)
Design, synthesis and evaluation of isaindigotone derivatives as acetylcholinesterase and butyrylcholinesterase inhibitors
Bioorganic & Medicinal Chemistry Lett 18 :3790

Pan L, Tan JH, Hou JQ, Huang SL, Gu LQ, Huang ZS (2008)
Bioorganic & Medicinal Chemistry Lett 18 :3790