Carlier_1999_Bioorg.Med.Chem.Lett_9_2335

Reference

Title : Potent, easily synthesized huperzine A-tacrine hybrid acetylcholinesterase inhibitors - Carlier_1999_Bioorg.Med.Chem.Lett_9_2335
Author(s) : Carlier PR , Du DM , Han Y , Liu J , Pang YP
Ref : Bioorganic & Medicinal Chemistry Lett , 9 :2335 , 1999
Abstract :

Hybrid acetylcholinesterase inhibitors composed of a key fragment of huperzine A and an intact tacrine unit were prepared. The syntheses are quite direct, proceeding in a maximum of 4 linear steps from commercially available starting materials. The optimum hybrid inhibitor (+/-)-9g is 13-fold more potent than (-)-huperzine A, and 25-fold more potent than tacrine.

PubMedSearch : Carlier_1999_Bioorg.Med.Chem.Lett_9_2335
PubMedID: 10476864

Related information

Citations formats

Carlier PR, Du DM, Han Y, Liu J, Pang YP (1999)
Potent, easily synthesized huperzine A-tacrine hybrid acetylcholinesterase inhibitors
Bioorganic & Medicinal Chemistry Lett 9 :2335

Carlier PR, Du DM, Han Y, Liu J, Pang YP (1999)
Bioorganic & Medicinal Chemistry Lett 9 :2335