The in vitro monoamine oxidase inhibitory (MAOI) activities of 11 heteroarylisopropylamines vis-a-vis MAO-A and MAO-B were described and interpreted in terms of possible interactions with the enzyme active site. Molecular dynamics simulations allowed a comparison between the most active MAO-A inhibitor of the series, the 1-(2-benzofuryl)-2-aminopropane, and the specific, analogous MAO-A substrate serotonin. (c) 2005 Elsevier Ltd. All rights reserved.
The in vitro monoamine oxidase inhibitory (MAOI) activities of 11 heteroarylisopropylamines vis-a-vis MAO-A and MAO-B were described and interpreted in terms of possible interactions with the enzyme active site. Molecular dynamics simulations allowed a comparison between the most active MAO-A inhibitor of the series, the 1-(2-benzofuryl)-2-aminopropane, and the specific, analogous MAO-A substrate serotonin. (c) 2005 Elsevier Ltd. All rights reserved.
Solid-phase synthesis of pyrroles from enaminones and nitroalkenes
作者:Axel W. Trautwein、Günther Jung
DOI:10.1016/s0040-4039(98)01887-5
日期:1998.11
A versatile solid-phase synthesis of pyrrole-3-carboxamides from enaminones and α-alkyl-α-nitroalkenes is presented. The reaction is performed either in a two or three component pathway by treating a polymer bound enaminone with a nitroalkene or an aldehyde and a nitroalkane respectively.