发明名称 Compounds
摘要 (I) Compounds of formula (I) or a pharmaceutically acceptable salt or solvate thereof wherein R1, R2 and R3 are as herein defined; R4 is a substitutent as herein defined or both R4 groups form a ring together with the carbon atoms to which they are attached to form a fused bicyclic ring containing from 8 to 12 atoms which may be saturated or unsaturated provided that when R1 is a substituted or unsubstituted pyrazolyl then R4 is not H and where both adjacent R4 groups form a ring with the atoms to which they are attached the adjacent R4 groups do not form an unsaturated carbocyclic ring with 6 carbon atoms; when R1 is a substituted or unsubstituted C6-10aryl then R4 is not H or methyl and where both adjacent R4 groups form a ring with the atoms to which they are attached the adjacent R4 groups do not form an unsaturated carbocyclic ring with 6 carbon atoms; and when R1 is a substituted or unsubstituted pyridyl then R4 is not methyl. The compound 4-fluoro-N-[[1-[4-(2-methylpyrazol-3-yl)phthalazin-1-yl]pyrrolidin-3-yl]methyl]-2-(trifluoromethyl)benzamide is also provided. The compounds of formula (I) are useful as inhibitors in the hedgehog signalling pathway, particularly Smoothened (Smo) in the treatment of cancer.
申请公布号 GB2528298(A) 申请公布日期 2016.01.20
申请号 GB20140012660 申请日期 2014.07.16
申请人 REDX PHARMA PLC 发明人 RICHARD ARMER;MATILDA BINGHAM;INDER BHAMRA;JONATHAN BEADLE;ANDREW MCCARROLL
分类号 C07D401/14;A61K31/501;A61K31/502;A61K31/5025;A61K31/513;A61P35/00;C07D403/14;C07D409/14;C07D413/14;C07D487/04 主分类号 C07D401/14
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