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Bioorg Med Chem Lett ; 23(10): 2948-50, 2013 May 15.
Article in English | MEDLINE | ID: mdl-23578689

ABSTRACT

Racemic 5-(trans-2-aminomethylcyclopropyl)indoles, 5-(trans-2-aminomethylcyclopentyl) indoles, and 5-(cis-2-aminomethylcyclopentyl)indoles were synthesized and evaluated as selective serotonin reuptake inhibitors. These analogs followed SAR trends similar to those previously reported for 3-cycloalkyl substituted indoles. The most potent analogs exhibited single digit nanomolar inhibition at the human serotonin transporter but were 10-fold less active than the previously reported compounds.


Subject(s)
Methylamines/pharmacology , Selective Serotonin Reuptake Inhibitors/pharmacology , Serotonin Plasma Membrane Transport Proteins/metabolism , Dose-Response Relationship, Drug , Humans , Methylamines/chemical synthesis , Methylamines/chemistry , Molecular Conformation , Molecular Structure , Selective Serotonin Reuptake Inhibitors/chemical synthesis , Selective Serotonin Reuptake Inhibitors/chemistry , Structure-Activity Relationship
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