申请人:Takeda Pharmaceutical Company Limited
公开号:US07514441B2
公开(公告)日:2009-04-07
There is provided a calcium receptor modulator comprising a compound of the formula (I):
wherein ring A is an optionally substituted 5- to 7-membered ring; ring B is an optionally substituted 5- to 7-membered heterocyclic ring; X1 is CR1, CR1R2, N or NR13; X2 is N or NR3; Y is C, CR4 or N, Z is CR5, CR5R6, N or NR7; Ar is an optionally substituted cyclic group; R is H, an optionally substituted hydrocarbon group, etc.; and is a single bond or a double bond; R1, R2, R3, R4, R5, R6, R7 and R13 are independently H, an optionally substituted hydrocarbon group; or a salt thereof or a prodrug thereof. Compounds of the formula (II) and (III):
wherein ring A is an optionally substituted 5- to 7-membered ring; Q is C, CR5 or N; R8, R9, R10, R11 and R12 are independently, H, an optionally substituted hydrocarbon group, etc., or a salt thereof are also provided. Also specify X1, R3, R1, Y and X3 in formula (II) and (III) as before.
提供了一种钙受体调节剂,包括式(I)的化合物:其中环A是可选取代的5-至7成员环;环B是可选取代的5-至7成员杂环;X1是CR1,CR1R2,N或NR13;X2是N或NR3;Y是C,CR4或N,Z是CR5,CR5R6,N或NR7;Ar是可选取代的环状基团;R是H,可选取代的烃基团等; 是单键或双键;R1、R2、R3、R4、R5、R6、R7和R13独立地是H,可选取代的烃基团;或其盐或前药。还提供了式(II)和(III)的化合物:其中环A是可选取代的5-至7成员环;Q是C,CR5或N;R8、R9、R10、R11和R12独立地是H,可选取代的烃基团等,或其盐。同样在式(II)和(III)中指定X1、R3、R1、Y和X3,如前所述。