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new benzamidinici derivatives with anti-inflammatory and immunosuppressive activity.

机译:具有抗炎和免疫抑制活性的新型苯甲酰胺基衍生物。

摘要

Compounds which can be represented by the general formula (I) indicated below: and in which: A is selected independently from the carboxamide group, the thiocarboxamide group, and the carbonyl group, R1 is selected from an alkyl group having from 1 to 3 carbon atoms and the amino group, unsubstituted or substituted with the nitro group or the methyl group, R2 is selected independently from hydrogen, an alkyl group having from 1 to 4 carbon atoms, the methoxy, ethoxy, propoxy group, a mono-, bi- or tricyclic cycloalkane residue having from 5 to 12 carbon atoms, the adamantyl group, an aryl, naphthyl or heterocyclic group, unsubstituted or substituted with methyl, methoxy, hydroxy, amino or halogen groups, R3 and R4 are selected independently from hydrogen and an alkyl group having from 1 to 3 carbon atoms, R5 represents one or two substituents independently selected from hydrogen and the methyl, methoxyl and hydroxyl groups, n is a whole number from 0 to 6, and the amidine group is in the para or meta position relative to the "-A-NH-" group.
机译:可以由下述通式(I)表示的化合物:其中:A独立地选自羧酰胺基,硫代羧酰胺基和羰基,R 1选自具有1-3个碳原子的烷基。 R 2是未被取代或被硝基或甲基取代的原子和氨基,R 2独立地选自氢,具有1-4个碳原子的烷基,甲氧基,乙氧基,丙氧基,单-,双-或具有5至12个碳原子的三环环烷烃残基,金刚烷基,芳基,萘基或杂环基,未被取代或被甲基,甲氧基,羟基,氨基或卤素取代,R3和R4独立地选自氢和烷基具有1至3个碳原子的基团,R 5代表一个或两个独立地选自氢和甲基,甲氧基和羟基的取代基,n为0至6的整数,并且group基为t相对于“ -A-NH-”组的对位或间位。

著录项

  • 公开/公告号ITTO20010110A1

    专利类型

  • 公开/公告日2002-08-08

    原文格式PDF

  • 申请/专利权人 ROTTA RESEARCH LABORATORIUM S.P.A.;

    申请/专利号IT2001TO00110

  • 申请日2001-02-08

  • 分类号C07D277/10;A61K31/167;A61K31/17;A61K31/404;A61K31/426;A61K31/4402;A61P1/04;A61P19/02;A61P29;A61P35;A61P37/02;A61P43;C07C257/14;C07C257/22;C07C279/18;C07C279/36;C07C335/20;C07D209/14;C07D209/40;C07D213/36;C07D213/40;C07D277/48;

  • 国家 IT

  • 入库时间 2022-08-22 00:42:20

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