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CHINAZOLINONE HEMMEN THE FARNESYLTRANSFERASE

机译:中唑啉酮的人法呢基转移酶

摘要

This invention concerns compounds of formulathe pharmaceutically acceptable acid addition salts and the stereochemically isomeric forms thereof, wherein the dotted line represents an optional bond; X is oxygen or sulfur; R1 and R2 each independently are hydrogen, hydroxy, halo, cyano, C1-6alkyl, trihalomethyl, trihalomethoxy, C2-6alkenyl, C1-6alkyloxy, hydroxyC1-6alkyloxy, C1-6alkyloxyC1-6alkyloxy, C1-6alkyloxycarbonyl, aminoC1-6alkyloxy, mono- or di(C1-6alkyl)aminoC1-6alkyloxy, Ar1, Ar1C1-6alkyl, Ar1oxy, Ar1C1-6alkyloxy; or when on adjacent positions R1 and R2 taken together may form a bivalent radical; R3 and R4 each independently are hydrogen, halo, cyano, C1-6alkyl, C1-6alkyloxy, Ar1oxy, C1-6alkylthio, di(C1-6alkyl)amino, trihalomethyl, trihalomethoxy; R5 is hydrogen, halo, cyano, optionally substituted C1-6alkyl, C1-6alkyloxycarbonyl or Ar1; or a radical of formula -OR10, -SR10, -NR11R12; R6 is an optionally substituted imidazolyl moiety; R7 is hydrogen or C1-6alkyl provided that the dotted line does not represent a bond; R8 is hydrogen, C1-6alkyl or Ar2CH2 or Het1CH2; R9 is hydrogen, C1-6alkyl, C1-6alkyloxy or halo, or R8 and R9 taken together may form a bivalent radical; Ar1 and Ar2 are optionally substituted phenyl and Het1 is optionally substituted pyridinyl; having farnesyl transferase inhibiting activity; their preparation, compositions containing them and their use as a medicine.
机译:本发明涉及下式的化合物:药学上可接受的酸加成盐及其立体化学异构形式,其中虚线代表任选的键; X是氧或硫; R 1和R 2各自独立地是氢,羟基,卤素,氰基,C 1-6烷基,三卤甲基,三卤甲氧基,C 2-6烯基,C 1-6烷氧基,羟基C 1-6烷氧基,C 1-6烷氧基C 1-6烷氧基,C 1-6烷氧基羰基,氨基C 1-6烷氧基,单-或二(C 1-6烷基)氨基C 1-6烷氧基,Ar 1,Ar 1 C 1-6烷基,Ar 1氧基,Ar 1 C 1-6烷氧基;或或者当在相邻位置R1和R2上一起形成二价基团时; R3和R4各自独立地是氢,卤素,氰基,C1-6烷基,C1-6烷氧基,Ar1氧基,C1-6烷硫基,二(C1-6烷基)氨基,三卤甲基,三卤甲氧基; R5是氢,卤素,氰基,任选取代的C1-6烷基,C1-6烷氧羰基或Ar1;或式-OR10,-SR10,-NR11R12的基团; R6是任选取代的咪唑基部分; R7是氢或C1-6烷基,条件是虚线不代表键。 R8是氢,C1-6烷基或Ar2CH2或Het1CH2; R 9是氢,C 1-6烷基,C 1-6烷氧基或卤素,或R 8和R 9一起可以形成二价基团; Ar 1和Ar 2是任选取代的苯基,Het 1是任选取代的吡啶基;具有法呢基转移酶抑制活性;它们的制剂,含有它们的组合物及其作为药物的用途。

著录项

  • 公开/公告号DE69838025T2

    专利类型

  • 公开/公告日2008-05-08

    原文格式PDF

  • 申请/专利权人 JANSSEN PHARMACEUTICA N.V.;

    申请/专利号DE1998638025T

  • 发明设计人

    申请日1998-04-17

  • 分类号C07D403/06;C07D405/04;A61K31/505;C07D401/14;

  • 国家 DE

  • 入库时间 2022-08-21 19:47:34

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