首页> 外国专利> New inhibitors n-myristoyl transferase, their preparation process and pharmaceutical compositions containing them.

New inhibitors n-myristoyl transferase, their preparation process and pharmaceutical compositions containing them.

机译:新抑制剂正肉豆蔻酰基转移酶,其制备方法和包含它们的药物组合物。

摘要

The invention relates to compounds of formula (I): USED AS INHIBITORS OF N-myristoyltransferase, in which R SUB 1 is a hydrogen atom, an alkyl group (C SUB 1-C SUB 6) substituted or unsubstituted, substituted phenyl or unsubstituted cycloalkyl, (C 3-C SUB SUB 7) methyl, (IMIDAZOLI-2-YL) mETHYL substituted or unsubstituted, (INDOL-3-YL) mETHYL substituted or unsubstituted, (1 -ARAINDOLIZIN-2 -yl) methyl, R SUB 2, R SUB 3 identical or different, represent a hydrogen atom or an alkyl group (C 1-C SUB SUB 6), or when R SUB 1 is a hydrogen atom, R SUB 2 SUB YR 3 formed with carbon atoms and nitrogen which they are attached, a heterocycle mono-, bi- or tricyclic, X represents a group -CO-, -SO SUB 2-, -PO (OH) -, Y represents a SUB GROUP -COR 5 (C SUB SUB 6-C 21) alkyl, substituted or substituted phenyl wherein, as appropriate, one or more groups methylenes may be replaced by an oxygen atom, OR SULFUR NUCLEO P.FENILENO, its isomers, diastereoisomers and epimers as well as their addition salts with an acid or a pharmaceutically acceptable base. MEDICINES.
机译:本发明涉及式(I)的化合物:用作N-肉豆蔻酰基转移酶的抑制剂,其中R SUB 1是氢原子,被取代或未被取代的烷基(C SUB 1-C SUB 6),被取代的苯基或未被取代的环烷基,(C 3-C SUB SUB 7)甲基,(咪唑啉-2-基)甲基取代或未取代的,(INDOL-3-YL)甲基取代或未取代的,(1-ARAINDOLIZIN-2-基)甲基,R SUB 2 R SUB 3相同或不同,表示氢原子或烷基(C 1 -C SUB SUB 6),或者当R SUB 1为氢原子时,R SUB 2 SUB YR 3由碳原子和氮形成连接的是杂环单,双或三环,X代表基团-CO-,-SO SUB 2-,-PO(OH)-,Y代表SUB GROUP -COR 5(C SUB SUB 6-C 21 )烷基,取代或取代的苯基,其中一个或多个亚甲基可以适当地被一个氧原子取代,或SULFUR NUCLEO P.FENILENO,其异构体,非对映异构体和差向异构体及其加成盐含有酸或药学上可接受的碱。药物。

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