Facile synthesis of substituted trans-2-arylcyclopropylamine inhibitors of the human histone demethylase LSD1 and monoamine oxidases A and B
摘要:
A facile synthetic route to substituted trans-2-arylcyclopropylamines was developed to provide access to mechanism-based inhibitors of the human flavoenzyme oxidase lysine-specific histone demethylase LSD1 and related enzyme family members such as monoamine oxidases A and B. (c) 2008 Elsevier Ltd. All rights reserved.
Compounds of a certain formula (I)
in which Ra and Rb have the meanings indicated in the description, are novel effective compounds with anti-proliferative and apoptosis inducing activity.
[EN] NOVEL MORPHINANS USEFUL FOR TREATING MEDICAL DISORDERS<br/>[FR] NOUVEAUX MORPHINANES UTILES POUR LE TRAITEMENT DE TROUBLES MÉDICAUX
申请人:HUMANWELL PHARMACEUTICAL US
公开号:WO2020205735A1
公开(公告)日:2020-10-08
The present invention related to novel morphinans, compositions comprising the novel morphinans, and their uses as agonists of the kappa opioid receptor.
Compounds of a certain formula (I), in which Ra and Rb have the meanings indicated in the description, are novel effective compounds with anti-proliferative and apoptosis inducing activity.