Several N-(indol-3-ylglyoxylyl)amino acid derivatives were synthesized and tested for their affinity for the benzodiazepine receptor in bovine cortical membranes. From these compounds, the N-[(5-chloro-, 5-bromo-, or 5-nitroindol-3-yl)glyoxylyl]glycine or -alanine esters were clearly the most potent, while the 5-methoxy analogues were considerably less active. Moreover, esters were more active than the corresponding acids. It is concluded that the affinity of these derivatives for the benzodiazepine receptor is profoundly dependent on amino acid molecular size, as well as the hydrophobic and electronic properties of the compounds.
|Autori:||MARTINI C; GERVASIO T; LUCACCHINI A; DASETTIMO A; PRIMOFIORE G; MARINI AM|
|Titolo:||SPECIFIC-INHIBITION OF BENZODIAZEPINE RECEPTOR-BINDING BY SOME N-(INDOL-3-YLGLYOXYLYL)AMINO ACID-DERIVATIVES|
|Anno del prodotto:||1985|
|Digital Object Identifier (DOI):||10.1021/jm00382a022|
|Appare nelle tipologie:||1.1 Articolo in rivista|