Substituted 2-(2,6-dioxopiperidin-3-yl)-phthalimides and-1-oxoisoindolines and method of reducing TNFalpha levels
申请人:——
公开号:US20020173658A1
公开(公告)日:2002-11-21
Substituted 2-(2,6-dioxopiperidin-3-yl)phthalimides and 1-oxo-2-(2,6-dioxopiperidin-3-yl)isoindolines reduce the levels of TNF&agr; in a mammal. A typical embodiment is 1-oxo-2-(2,6-dioxo-3-methylpiperidin-3-yl)-4,5,6,7-tetrafluoroisoindoline.
Substituted 2-(2,6-dioxopiperidin-3-yl)-phthalimides and 1-oxoisoindolines and method of reducing TNF alpha levels
申请人:CELGENE CORPORATION
公开号:EP2859895A1
公开(公告)日:2015-04-15
Substituted 2-(2,6-dioxopiperidin-3-yl)phthalimides and 1-oxo-2-(2,6-dioxopiperidin-3-yl)isoindolines reduce the levels of TNFα in a mammal. Typical embodiments are 1-oxo-2-(2,6-dioxo-3-methylpiperidin-3-yl)-4,5,6,7-tetrafluoroisoindoline and 1,3-dioxo-2-(2,6-dioxo-3-methylpiperidin-3-yl)-4-aminoisoindoline.
Substituted 2-(2,6-Dioxopiperidin-3-yl)-phthalimides and 1-Oxoisoindolines and Method of Reducing TNFalpha Levels
申请人:Muller George W.
公开号:US20130030021A1
公开(公告)日:2013-01-31
Substituted 2-(2,6-dioxopiperidin-3-yl)phthalimides and 1-oxo-2-(2,6-dioxopiperidin-3-yl)isoindolines are disclosed. The compounds are useful, for example, in reducing the levels of TNFα in a mammal.
Substituted 2-(2,6-dioxopiperidin-3-yl)phthalimides and 1-oxo-2-(2,6-dioxopiperidin-3-yl)isoindolines are disclosed. The compounds are useful, for example, in reducing the levels of TNFα in a mammal.
[EN] SUBSTITUTED 2-(2,6-DIOXOPIPERIDIN-3-YL)-PHTHALIMIDES AND 1-OXOISOINDOLINES AND METHOD OF REDUCING TNF alpha LEVELS<br/>[FR] 1-OXOISOINDOLINES ET 2-(2,6-DIOXOPIPERIDIN-3-YL)-PHTALIMIDES SUBSTITUES ET PROCEDE POUR REDUIRE LES TAUX DE FNT ALPHA
申请人:CELGENE CORPORATION
公开号:WO1998054170A1
公开(公告)日:1998-12-03
(EN) Substituted 2-(2,6-dioxopiperidin-3-yl)-phthalimides and 1-oxo-2-(2,6-dioxopiperidin-3-yl)isoindolines reduce the levels of TNF$g(a) in a mammal. A typical embodiment is 1-oxo-2-(2,6-dioxo-3-methylpiperidin-3-yl)-4,5,6,7-tetrafluoroisoindoline.(FR) Ces 2-(2,6-dioxopipéridin-3-yl)-phtalimides et 1-oxo-2-(2,6-dioxopipéridin-3-yl)iso-indolines substitués permettent de réduire les taux de FNT$g(a) chez un mammifère. Dans une forme d'application typique, on utilise du 1-oxo-2-(2,6-dioxo-3-méthylpipéridin-3-yl)-4,5,6,7-tetrafluoroisoindoline.