发明名称 Carboxamide compounds and methods for using the same
摘要 Disclosed are carboxamide compounds, as well as pharmaceutical compositions and methods of use. One embodiment is a compound having the structure; in which R1, R2, R3, R4, D, J, Z, T, p, q, w and x are as described herein. In certain embodiments, a compound disclosed herein activates the AMPK pathway, and can be used to treat metabolism-related disorders and conditions.
申请公布号 US9062052(B2) 申请公布日期 2015.06.23
申请号 US201414493050 申请日期 2014.09.22
申请人 Rigel Pharmaceuticals, Inc. 发明人 Yu Jiaxin;Hong Hui;Darwish Ihab S.;Xu Xiang;Singh Rajinder
分类号 A61K31/437;C07D471/04;C07D211/58;C07D401/12;C07D401/14;C07D413/12;C07D413/14;C07D417/14;C07D487/08 主分类号 A61K31/437
代理机构 McDonnell Boehnen Hulbert & Berghoff LLP 代理人 Young Travis;McDonnell Boehnen Hulbert & Berghoff LLP
主权项 1. A compound having the structural formulaor a pharmaceutically acceptable salt or N-oxide thereof, wherein R1 is H, —(C1-C4 alkyl),—C(O)—(C1-C4 alkyl) or —C(O)O—(C1-C4 alkyl); each R15 is independently selected from —(C1-C3 alkyl), —(C1-C3 haloalkyl), —(C0-C3 alkyl)-L-R7, —(C0-C3 alkyl)-NR8R9, —(C0-C3 alkyl)-OR10 , —(C0-C3 alkyl)-C(O)R10, —(C0-C3 alkyl)-S(O)0-2R10 , -halogen, —NO2 and —CN and two R15 on the same carbon optionally combine to form oxo; v is 0, 1, 2, 3 or 4; G is —S(O)2—, L, or —(C0-C3 alkyl)-, in which each carbon of the —(C0-C3 alkyl)- is optionally and independently substituted with one or two R16; R17 is aryl or heteroaryl, optionally substituted with 1, 2or 3 substituents independently selected from —(C1-C3 alkyl), —(C1-C3 haloalkyl), —(C0-C3 alkyl)-L-R7, —(C0-C3 alkyl)-NR8R9, —(C0-C3 alkyl)-OR10, —(C0-C3 alkyl)-C(O)R10 , —(C0-C3 alkyl)-S(O)0-2 R10, -halogen, —NO2 and —CN; each R3 is independently selected from —(C1-C3 alkyl), —(C1-C3 haloalkyl), —(C0-C3 alkyl)-L-R7 , —(C0-C3 alkyl)-NR8R9, —(C0-C3 alkyl)-OR10, —(C0-C3 alkyl)-C(O)R10, —(C0-C3 alkyl)-S(O)0-2R10, -halogen, —NO2 and —CN; w is 0, 1, 2 or 3; each R4 is independently selected from —(C1-C3 alkyl), —(C1-C3 haloalkyl), —(C0-C3 alkyl)-L-R7, —(C0-C3 alkyl)-NR8R9, —(C0-C3 alkyl)-OR10, —(C0-C3 alkyl)-C(O)R10, —(C0-C3 alkyl)-S(O)0-2R10, -halogen, —NO2 and —CN, and two R4 groups optionally combine to form an oxo; x is 0, 1, 2, 3 or 4; Q is —S(O)2—, L, or —(C0-C3 alkyl)-, in which each carbon of the —(C0-C3 alkyl)- is optionally and independently substituted with one or two R16; the ring denoted by “A” is heteroaryl or aryl; each R5 is independently selected from —(C1-C3 alkyl), —(C1-C3 haloalkyl), —(C0-C3 alkyl)-L-R7, —(C0-C3 alkyl)-NR8R9, —(C0-C3 alkyl)-OR10, —(C0-C3 alkyl)-C(O)R10, —(C0-C3 alkyl)-S(O)0-2R10, -halogen, —NO2 and —CN; y is 0, 1, 2, 3 or 4; in which each L is independently selected from —NR9C(O)O —, —OC(O)NR9—, —NR9C(O)—NR9—, —NR9C(O)S —, —SC(O)NR9—, —NR9C(O)—, —C(O)—NR9—, —NR9C(S)O —, —OC(S)NR9—, —NR9C(S)—NR9—, —NR9C(S)S—, —SC(S)NR9—, —NR9C(S)—, —C(S)NR9—, —SC(O)NR9—, —NR9C(S)—, —S(O)0-2—, —C(O)O, —OC(O)—, —C(S)O—, —OC(S)—, —C(O)S—, —SC(O)—, —C(S)S—, —SC(S)—, —OC(O)O—, —SC(O)O—, —OC(O)S—, —SC(S)O—, —OC(S)S—, —NR9SO2—, —SO2NR9—and —NR9SO2NR9—,each R7, R8 and R10is independently selected from H, —(C1-C2 alkyl), —(C1-C2 haloalkyl), —(C0-C2 alkyl)-L-(C0-C2 alkyl), —(C0-C2 alkyl)-NR9(C0-C2 alkyl), —(C0-C 2 alkyl)-O—(C0-C2 alkyl), —(C0-C2 alkyl)-C(O)—(C0-C 2 alkyl) and —(C0-C 2 alkyl)-S(O)0-2—(C0-C2 alkyl),each R9 is independently selected from —H, —(C1-C4 alkyl), —C(O)—(C1-C4 alkyl) and —C(O)O—(C1-C4 alkyl), andeach R16 is independently selected from —(C1-C3 alkyl), —(C1-C3 haloalkyl), —(C0-C3 alkyl)-L-R7, —(C0-C3 alkyl)-NR8R9, —(C0-C3 alkyl)-OR10, —(C0-C3 alkyl)-C(O)R10, —(C0-C3 alkyl)-S(O)0-2R10, -halogen, —NO2 and —CN, and two R16 on the same carbon optionally combine to form an oxo.
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