发明名称 SUBSTITUTED 2-(2,6-DIOXO-3-FLUOROPIPERIDIN-3-YL)-ISOINDOLINES AND THEIR USE TO REDUCE TNF.ALPHA. LEVELS
摘要 A chiral compound is described, in racemic, (R)- or (S)- form, which is a 2-(2,6-dioxo-3-fluoropiperidin-3-yl)- isoindoline of the formula: (see formula I) in which Y is oxygen or H2 and each of R1, R2, R3, and R4, independently of the others, is hydrogen, halo, alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms, or amino, or the acid addition salts of said 2-(2,6-dioxo-3- fluoropiperidin-3-yl)-isoindolines which contain a nitrogen atom capable of being protonated. 1-Oxo-2-(2,6-dioxo-3- fluoropiperidin-3-yl)-isoindolines and 1,3-dioxo-2-(2,6- dioxo-3-fluoropiperidin-3-yl)-isoindolines reduce the levels of inflammatory cytokines such as TNF.alpha. in a mammal. A typical embodiment is 1,3-dioxo-2-(2,6-dioxo-3--fluoropiperidin-3-yl)- isoindoline.
申请公布号 CA2317834(C) 申请公布日期 2007.07.24
申请号 CA19982317834 申请日期 1998.11.17
申请人 CELGENE CORPORATION 发明人 MULLER, GEORGE W.;STIRLING, DAVID I.;MAN, HON-WAH;CHEN, ROGER SHEN-CHU
分类号 C07D401/04;A61K31/4427;A61K31/4439;A61K31/445;A61K31/452;A61K31/4523;A61P17/06;A61P19/02;A61P29/00;A61P31/08;A61P31/10;A61P33/06;A61P35/00;A61P43/00;C07D 主分类号 C07D401/04
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