[EN] 3-(2-(AMINOETHYL)-INDOL-4-OL DERIVATIVES, METHODS OF PREPARATION THEREOF, AND THE USE AS 5-HT2 RECEPTOR MODULATORS [FR] DÉRIVÉS DE 3-(2-(AMINOÉTHYL)-INDOL-4-OL, LEURS PROCÉDÉS DE PRÉPARATION ET LEUR UTILISATION EN TANT QUE MODULATEURS DU RÉCEPTEUR 5-HT2
Konformation und Rotationsbarrieren substituierter Glyoxylsäureamide
摘要:
Semiempirical calculations predict an orthogonal orientation of the carbonyl groups in tertiary glyoxylic acid amides, which is in good agreement with an X-ray structure analysis of 5. Due to the influence of the a-carbonyl group, the rotation barrier in the substituted glyoxylic acid amides 2a-d, 3a, 3b, and 4-6 (Delta G(c)(#)=84-92 kJ mol(-1)) is about 10 kJ/mol higher than in simple acid amides, as was found by dynamic NMR line shape analysis.
[EN] 3-ETHYLAMINO-INDOLE DIMERS AS SEROTONERGIC AGENTS USEFUL FOR THE TREATMENT OF DISORDERS RELATED THERETO<br/>[FR] DIMÈRES DE 3-ÉTHYLAMINO-INDOLE EN TANT QU'AGENTS SÉROTONINERGIQUES UTILES POUR LE TRAITEMENT DE TROUBLES ASSOCIÉS À CEUX-CI
申请人:[en]MINDSET PHARMA INC.
公开号:WO2024026573A1
公开(公告)日:2024-02-08
The present application relates to 3-ethylamino-indole dimers of general Formula I, to processes for their preparation, to compositions comprising them and to their use in activation of a serotonin receptor in a cell, as well as to treating diseases, disorders or conditions by activation of a serotonin receptor in or on a cell. The diseases, disorders or conditions include, for example, psychosis, mental illnesses and CNS disorders.