The present invention is directed to tricyclic compounds, pharmaceutically acceptable compositions comprising compounds of the invention and methods of using said compositions in the treatment of various disorders.
[EN] TRICYCLIC COMPOUNDS AS ANTICANCER AGENTS<br/>[FR] COMPOSÉS TRICYCLIQUES UTILISÉS EN TANT QU'AGENTS ANTICANCÉREUX
申请人:BRISTOL MYERS SQUIBB CO
公开号:WO2016183114A1
公开(公告)日:2016-11-17
The present invention is directed to tricyclic compounds, pharmaceutically acceptable compositions comprising compounds of the invention and methods of using said compositions in the treatment of various disorders.
[EN] 5H-PYRIDO[3,2-B]INDOLE COMPOUNDS AS ANTICANCER AGENTS<br/>[FR] COMPOSÉS 5H-PYRIDO[3,2-B]INDOLE EN TANT QU'AGENTS ANTICANCÉREUX
申请人:BRISTOL MYERS SQUIBB CO
公开号:WO2016183115A1
公开(公告)日:2016-11-17
The present invention is directed to tricyclic compounds of formula (I), pharmaceutically acceptable compositions comprising compounds of the invention and said compositions for use in methods for the treatment of various disorders in particular cancer.
Described herein are compounds that are somatostatin modulators, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds in the treatment of conditions, diseases, or disorders that would benefit from modulation of somatostatin activity.
SYNTHETIC METHODOLOGY FOR THE REDUCTIVE ALKYLATION AT THE C-3 POSITION OF INDOLES
申请人:Michalak Ronald S.
公开号:US20080161581A1
公开(公告)日:2008-07-03
A process for the reductive alkylation at the C-3 position of an indole compound in which the indole is treated with an aldehyde in the presence of a Lewis acid and a silicon hydride reducing agent. The process is useful for alkylating the C-3 position of indoles that contain acid-sensitive substituents at the N-1 position.