Brufani_1994_Farmaco_40_743

Reference

Title : Synthesis of 2'-heptylcarbamoyloxy-2-methyl-6,7-benzomorphan: a new analogue of heptylphysostigmine (MF 201) - Brufani_1994_Farmaco_40_743
Author(s) : Brufani M , Filocamo L , Imbriani E , Lappa S , Mannina L
Ref : Farmaco , 40 :743 , 1994
Abstract :

The synthesis of 2'-heptylcarbamoyloxy-2-methyl-6,7-benzomorphan is described. The compound is structurally related to the cholinesterase inhibitor heptylphysostigmine (MF 201) because the angular methyl group of the esoroline nucleus has been changed into a bridging carbon and the anilinic nitrogen has been replaced by a methylene group. This compound proved to be a potent cholinesterase in vitro inhibitor.

PubMedSearch : Brufani_1994_Farmaco_40_743
PubMedID: 7832976

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Citations formats

Brufani M, Filocamo L, Imbriani E, Lappa S, Mannina L (1994)
Synthesis of 2'-heptylcarbamoyloxy-2-methyl-6,7-benzomorphan: a new analogue of heptylphysostigmine (MF 201)
Farmaco 40 :743

Brufani M, Filocamo L, Imbriani E, Lappa S, Mannina L (1994)
Farmaco 40 :743