Heller_2016_Eur.J.Med.Chem_126_652

Reference

Title : Amino derivatives of platanic acid act as selective and potent inhibitors of butyrylcholinesterase - Heller_2016_Eur.J.Med.Chem_126_652
Author(s) : Heller L , Kahnt M , Loesche A , Grabandt P , Schwarz S , Brandt W , Csuk R
Ref : Eur Journal of Medicinal Chemistry , 126 :652 , 2016
Abstract :

A set of thirtyfive 30-norlupan derivatives (2-36) was prepared from the natural triterpenoid platanic acid (PA), and the hydroxyl group at C-3, the carboxyl group at C-17 and the carbonyl group at C-20 were modified. These derivatives were tested for their inhibitory activity for the enzymes acetylcholinesterase (AChE, from electric eel) and butyrylcholinesterase (BChE, from equine serum) using Ellman's assay. Extra enzyme kinetic studies were performed. The most active compound was (3beta, 20R)-3-acetyloxy-20-amino-30-norlupan-28-oate (32) showing a Ki value of 0.01 +/- 0.003 muM for BChE. This compound proved to be a selective (FB = 851), mixed-type inhibitor for BChE.

PubMedSearch : Heller_2016_Eur.J.Med.Chem_126_652
PubMedID: 27936444

Related information

Citations formats

Heller L, Kahnt M, Loesche A, Grabandt P, Schwarz S, Brandt W, Csuk R (2016)
Amino derivatives of platanic acid act as selective and potent inhibitors of butyrylcholinesterase
Eur Journal of Medicinal Chemistry 126 :652

Heller L, Kahnt M, Loesche A, Grabandt P, Schwarz S, Brandt W, Csuk R (2016)
Eur Journal of Medicinal Chemistry 126 :652