Title : Effect of cholinesterase inhibition in vitro by huperzine analogs - Tang_1994_Zhongguo.Yao.Li.Xue.Bao_15_107 |
Author(s) : Tang XC , Xu H , Feng J , Zhou TX , Liu JS |
Ref : Acta Pharmacol Sin , 15 :107 , 1994 |
Abstract :
Huperzine (Hup) A and B were first discovered and studied by Chinese. Fourteen analogs of Hup were tested for their anticholinesterase (anti-ChE) activity by colorimetric method using rat erythrocyte membrane and serum as enzyme sources. Hup-A showed the highest anti-AChE potency. The anti-BCHE activity of (-)dihydro and (-)tetrahydro analogs were potent than those of Hup-A. Their anti-AChE activities were comparable to those of physostigmine and galanthamine. Dihydro analog inhibition was of the mixed competitive type with a Ki value of 0.12 mumol.L-1. Tetrahydro analog inhibition was of the competitive type with a Ki value of 0.56 mumol.L-1. They were different from isoflurophate to bond to AChE in a reversible manner. |
PubMedSearch : Tang_1994_Zhongguo.Yao.Li.Xue.Bao_15_107 |
PubMedID: 8010100 |
Tang XC, Xu H, Feng J, Zhou TX, Liu JS (1994)
Effect of cholinesterase inhibition in vitro by huperzine analogs
Acta Pharmacol Sin
15 :107
Tang XC, Xu H, Feng J, Zhou TX, Liu JS (1994)
Acta Pharmacol Sin
15 :107