首页> 外国专利> New 1,3-disubstituted cycloheptene derivatives, are selective farnesyl transferase inhibitors useful for treating cancer diseases, restenosis or type I neurofibromatosis

New 1,3-disubstituted cycloheptene derivatives, are selective farnesyl transferase inhibitors useful for treating cancer diseases, restenosis or type I neurofibromatosis

机译:新的1,3-二取代的环庚烯衍生物是选择性的法呢基转移酶抑制剂,可用于治疗癌症,再狭窄或I型神经纤维瘤病

摘要

Compound of formula (I):wherein:X represents a bond or alkylene, CO, S(O)n, -S(O)n-A1-, -CO-A1-, -A-S(O)n-A'1- or -A1-CO-A'1-,Y represents aryl, heteroaryl, cycloalkyl or heterocycloalkyl, each unsubstituted or substituted,R1, R2, R3 and R4 each independently of the others represent hydrogen or aryl, heteroaryl, cycloalkyl or heterocycloalkyl, each unsubstituted or substituted,or R1, R2, R3 and R4, taken in pairs, together form a bond, or form a fused benzene ring or a fused aromatic or partially unsaturated heterocycle,T represents -CH(R5)-, -N(R5)- or -N(R5)CO-,V represents hydrogen or unsubstituted or substituted aryl or heteroaryl,A2 represents [C(R6)(R'6)]p,R7 and R8 are as defined in the description,their isomers and addition salts thereof with a pharmaceutically acceptable acid or base and medicinal products containing the same are useful as farnesyl transferase inhibitors.
机译:式(I)的化合物:其中:X表示键或亚烷基,CO,S(O)n,-S(O)n-A1-,-CO-A1-,-AS(O)n-A'1 -或-A1-CO-A'1-,Y代表未取代或取代的芳基,杂芳基,环烷基或杂环烷基,R1,R2,R3和R4各自独立地表示氢或芳基,杂芳基,环烷基或杂环烷基,成对的每个未取代或取代的或R1,R2,R3和R4一起形成键或形成稠合的苯环或稠合的芳族或部分不饱和杂环,T代表-CH(R5)-,-N( R5)-或-N(R5)CO-,V表示氢或未取代或取代的芳基或杂芳基,A2表示[C(R6)(R'6)] p,R7和R8如说明书中所定义,它们的异构体以及其与药学上可接受的酸或碱的加成盐以及包含其的药用产品可用作法呢基转移酶抑制剂。

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