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Deuterated isoindolin-1,3-dione derivatives as PDE4 and TNF-alpha inhibitors

机译:氘代异吲哚啉-1,3-二酮衍生物作为PDE4和TNF-α抑制剂

摘要

A compound of Formula I: ** Formula ** or a pharmaceutically acceptable salt thereof, wherein: R1 is selected from CH3, CH2D, CHD2 and CD3; R2 is CH3 or CD3; R3 is CD3; R4 is an ethyl group substituted with zero to five deuterium atoms, or is a cyclopentyl group substituted with zero to nine deuterium atoms; X is selected from CH2, CHD, CD2 and C = O; each of Y1a, Y1b, Y2, Y3, Y4, Y5, Y7 and Y8 is independently selected from H and D; Y6 is selected from Cl, H and D; and in which the isotopic enrichment factor for each designated deuterium atom is at least 6,000.
机译:式I的化合物:式**或其药学上可接受的盐,其中:R1选自CH3,CH2D,CHD2和CD3; R2是CH3或CD3; R3是CD3; R 4为被0〜5个氘原子取代的乙基,或为被0〜9个氘原子取代的环戊基。 X选自CH 2,CHD,CD 2和C> = O; Y1a,Y1b,Y2,Y3,Y4,Y5,Y7和Y8各自独立地选自H和D; Y6选自Cl,H和D;并且其中每个指定的氘原子的同位素富集因子至少为6,000。

著录项

  • 公开/公告号ES2568629T3

    专利类型

  • 公开/公告日2016-05-03

    原文格式PDF

  • 申请/专利权人 CONCERT PHARMACEUTICALS INC.;

    申请/专利号ES20130190362T

  • 发明设计人 LIU JULIE F.;

    申请日2010-06-15

  • 分类号C07B59;

  • 国家 ES

  • 入库时间 2022-08-21 14:22:11

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