首页> 外国专利> New benzocycloheptenyl-alkanoic acid derivatives and analogs are selective vitronectin receptor antagonists useful e.g. for treating cardiovascular or inflammatory diseases or especially cancer

New benzocycloheptenyl-alkanoic acid derivatives and analogs are selective vitronectin receptor antagonists useful e.g. for treating cardiovascular or inflammatory diseases or especially cancer

机译:新的苯并环庚烯基-链烷酸衍生物和类似物是有用的选择性玻连蛋白受体拮抗剂,例如可用于药物治疗。用于治疗心血管或炎性疾病,尤其是癌症

摘要

Compounds of formula (1):wherein:G represents an optionally substituted phenyl or optionally substituted heterocycle, G1 and G2 being N or C,T1 represents -CH2-CH2-, -CH=CH- or =CH-CH2-, and T2 is a bond, or T1 represents -CH2- or =CH- and T2 is -CH2-, =CH-,R5 represents -(CH2)m-COOR6,R6 and R6' represent hydrogen, alkyl, optionally substituted aryl or optionally substituted arylalkyl,A represents -CO-, -CH2-, =CH- or -CH= and W represents -CH-, =C- or -C=, or A represents -CO- or -CH2- and W represents N,X represents -CO-X1-, -CO-NR6-X1-, -NR6-CO-X1-, -O-X1-, -SO2-NR6-X1- or -S(O)n-X1-,Y represents -Y1-, -Y2-Y1- or -Y1-Y2-Y1-, Y1 being an alkylene, alkenylene or alkynylene, and Y2 being an arylene, heteroarylene, cycloalkylene or heterocycloalkylene,Z represents -Z1-, -Z10-NR6-, and -Z10-NR6-CO-, Z1 being a heteroaryl, heterocycloalkyl, heteroarylalkyl, heterocycloalkylalkyl, fused arylheteroaryl, fused arylheterocycloalkyl, fused heteroarylheterocycloalkyl, fused heterocycloalkylheteroaryl or fused heteroarylheteroaryl, each of which is optionally substituted, or a group,Z2-NR6 or Z2-NR6-CO, Z2 being a group Z1, alkyl or heteroalkyl, andZ10 represents Z1 or an alkyl,its enantiomers, diastereoisomers, and addition salts thereof with a pharmaceutically acceptable acid or base,and medicinal products containing the same which are useful as vitronectin receptor antagonists.
机译:式(1)的化合物:其中:G代表任选取代的苯基或任选取代的杂环,G1和G2为N或C,T1代表-CH2-CH2-,-CH = CH-或= CH-CH2-,和T2是键,或T1代表-CH2-或= CH-,且T2是-CH2-,= CH-,R5代表-(CH2)m-COOR6,R6和R6'代表氢,烷基,可选被取代的芳基或可选被取代芳烷基,A代表-CO-,-CH2-,= CH-或-CH =,W代表-CH-,= C-或-C =,或A代表-CO-或-CH2-,W代表N,X代表-CO-X1-,-CO-NR6-X1-,-NR6-CO-X1-,-O-X1-,-SO2-NR6-X1-或-S(O)n-X1-,Y代表- Y 1-,-Y 2 -Y 1-或-Y 1 -Y 2 -Y 1-,Y 1为亚烷基,亚烯基或亚炔基,并且Y 2为亚芳基,杂亚芳基,亚环烷基或杂环亚烷基,Z表示-Z 1-,-Z 10 -NR 6-,和-Z 10 -NR 6 -CO-,Z 1为杂芳基,杂环烷基,杂芳基烷基,杂环烷基烷基,稠合的芳基杂芳基,稠合的芳基杂环烷基,稠合的杂芳基杂环烷基,稠合的杂环烷基杂合物各自任选被取代的芳基或稠合的杂芳基杂芳基或基团Z2-NR6或Z2-NR6-CO,Z2为基团Z1,烷基或杂烷基,且Z10代表Z1或烷基,其对映异构体,非对映异构体和加成基其与药学上可接受的酸或碱形成的盐以及包含其的药物产品可用作玻连蛋白受体拮抗剂。

著录项

  • 公开/公告号NO324052B1

    专利类型

  • 公开/公告日2007-08-06

    原文格式PDF

  • 申请/专利权人 LES LABORATOIRES SERVIER;

    申请/专利号NO20020004275

  • 申请日2002-09-06

  • 分类号C07D233/24;A61K31/4164;A61K31/4168;A61K31/417;A61K31/4184;A61K31/426;A61K31/4375;A61K31/44;A61K31/4402;A61K31/505;A61K31/55;A61P9;A61P19/10;A61P27/02;A61P29;A61P33/14;A61P35;A61P43;C07D213/36;C07D213/74;C07D223/04;C07D223/12;C07D233/48;C07D233/54;C07D235/10;C07D235/14;C07D235/30;C07D239/14;C07D277/18;C07D277/20;C07D277/42;C07D401/12;C07D403/12;C07D471/04;

  • 国家 NO

  • 入库时间 2022-08-21 20:56:48

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