发明名称 Sigma receptors ligands with anti-apoptotic and/or pro-apoptotic properties, over cellular mechanisms, exhibiting prototypical cytoprotective and also anti-cancer activity
摘要 The present invention involves new and original sigma receptors ligands: (Mono- or dialkylaminoalkyl)-γ-butyrolactones, their analogues aminotetrahydroturanes, the (1-adamantyl)benzene alkylamines, the N,N Dialkyl α-[(adamantyl-1)benzyloxy-2]alkylamines and the 3-cyclopentyl adamantyl-amines or alkylamines or -alkyl phenylamines, their enantiomers or diastereoisomers, their pharmaceutically acceptable salts and Quinacrine Me-thylene blue, Asteinizole and their relative analogues with pro-apoptotic and/or anti-apoptotic properties over cellular biochemical mechanisms, with prototypical anti-cancer, antimetastatic and antiviral activities associated with antagonism of the neuropatic pain and, at very low doses, with cytoprotective and cytoregenerative activity against the cytodegenerative diseases.
申请公布号 US9180106(B2) 申请公布日期 2015.11.10
申请号 US201414205637 申请日期 2014.03.12
申请人 Anavex Life Sciences Corp. 发明人 Vamvakides Alexandre
分类号 A61K31/495;A61K31/4453;A61K31/137;A61K31/365;A61K31/13;A61K31/341;A61K31/343;A61K31/431;A61K31/44;A61K31/445;A61K31/5377;A61K31/5415;A61K31/64;A61K31/4525 主分类号 A61K31/495
代理机构 Novak Druce Connolly Bove + Quigg LLP 代理人 Novak Druce Connolly Bove + Quigg LLP
主权项 1. A method of treating melanoma in a subject comprising administering in a subject in need thereof a therapeutic amount of a first compound shown hereand a therapeutic amount of a second compound selected from the group consisting of quinacrine, methylene blue, or astemizole.
地址 New York NY US