embedded image whereinR is an optionally substituted cyclic group or an optionally substituted carbamoyl group, provided that R is not an optionally substituted 7-pyrido[2,3-d]pyrimidyl group;ring A is an optionally further substituted pyridazine ring;R1, R2, R3, R4, R11, R12, R13 and R14 are each independently a hydrogen atom or a substituent, or R1 and R11 in combination, R2 and R12 in combination, R3 and R13 in combination, or R4 and R14 in combination optionally form an oxo group, or R2 and R4 in combination optionally form a bond or an alkylene cross-linkage;m and n are each independently an integer of 0 to 2;ring B is an optionally substituted ring, provided that the two atoms constituting ring B, which are adjacent to the spiro carbon atom, are not oxygen atoms at the same time,or a salt thereof, or a prodrug thereof."/> Spiro compounds having stearoyl-CoA desaturase action
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Spiro compounds having stearoyl-CoA desaturase action

机译:具有硬脂酰辅酶A去饱和酶作用的螺化合物

摘要

The present invention aims to provide a novel SCD inhibitor.;The present invention relate to SCD inhibitor comprising A compound represented by the formula (I); embedded image whereinR is an optionally substituted cyclic group or an optionally substituted carbamoyl group, provided that R is not an optionally substituted 7-pyrido[2,3-d]pyrimidyl group;ring A is an optionally further substituted pyridazine ring;R1, R2, R3, R4, R11, R12, R13 and R14 are each independently a hydrogen atom or a substituent, or R1 and R11 in combination, R2 and R12 in combination, R3 and R13 in combination, or R4 and R14 in combination optionally form an oxo group, or R2 and R4 in combination optionally form a bond or an alkylene cross-linkage;m and n are each independently an integer of 0 to 2;ring B is an optionally substituted ring, provided that the two atoms constituting ring B, which are adjacent to the spiro carbon atom, are not oxygen atoms at the same time,or a salt thereof, or a prodrug thereof.
机译:本发明的目的是提供一种新型的SCD抑制剂。本发明涉及包含式(I)表示的化合物的SCD抑制剂。 “嵌入式图像” 其中R为任选取代的环状基团或任选取代的氨基甲酰基,条件是R不是任选取代的7-吡啶并[2,3-d]嘧啶基;环A是任选地进一步取代的哒嗪环;R 1 ,R 2 ,R 3 ,R 4 ,R 11 , R 12 ,R 13 和R 14 分别独立地是氢原子或取代基,或R 1 和R 11 组合,R 2 和R 12 组合,R 3 和R 13 < / Sub>组合,或R 4 和R 14 组合形成一个氧代基团,或R 2 和R 4 组合可任选形成键或亚烷基交联;m和n分别独立地是0至2的整数;环B是一个可选取代的环,前提是构成环B的两个与螺碳原子相邻的原子同时不是氧原子,或其盐或其前药。

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