Jin_2003_Arzneimittelforschung_53_753

Reference

Title : Synthesis and docking studies of alkylene-linked dimers of (-)-huperzine A - Jin_2003_Arzneimittelforschung_53_753
Author(s) : Jin G , Luo X , He X , Jiang H , Zhang H , Bai D
Ref : Arzneimittelforschung , 53 :753 , 2003
Abstract :

(-)-Huperzine A (5, HupA), an alkaloid isolated from the herb Huperzia serrata, is a potent, selective and reversible acetylcholinesterase (AchE) inhibitor. Based on the hypothesis with respect to two binding sites in the active gorge of AChE and the good example of bis-tacrine, it was predicted from the docking studies of alkylene-linked dimers of HupA that dimers 6 (n = 5, 7, 9) might have good AChE inhibitory activity. Therefore, six dimers with 7-12 methylene units as tethers were thus prepared. It was found that these dimers were less potent than HupA in inhibition of AChE. The difference of the inhibitory potency between these dimers is coincident with the results of the docking studies.

PubMedSearch : Jin_2003_Arzneimittelforschung_53_753
PubMedID: 14677369

Related information

Citations formats

Jin G, Luo X, He X, Jiang H, Zhang H, Bai D (2003)
Synthesis and docking studies of alkylene-linked dimers of (-)-huperzine A
Arzneimittelforschung 53 :753

Jin G, Luo X, He X, Jiang H, Zhang H, Bai D (2003)
Arzneimittelforschung 53 :753