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INDOLE AND CARBAZOLE DERIVATIVES, PROCESS FOR THEIR PREPARATION, AND THEIR USE AS MRSA SENSITIVE ANTIBIOTICS

机译:吲哚和咔唑衍生物,其制备方法及其作为MRSA敏感抗生素的用途

摘要

The 1,3-bis(indol-3-yl)-tetrahydrocyclopenta[b]indoles, 1,4-bis(indol-3-yl)tetrahydrocarbazoles, 6,10-bis(indol-3-yl)hexahydrocyclohepta[b]indoles, 6,11-bis(indol-3-yl)hexahydrocycloocta[b]indoles and 11-(indol-3-yl)benzo[b]carbazoles of the general formulae and developed in accordance with the invention have a selective inhibiting effect on the growth of S. aureus and the methicillin-resistant S. aureus (MRSA) in the lower micro-molecular concentration range in a screening of additional Gram-positive and Gram-negative bacteria and fungi. The production of the compounds from dialdehydes and indoles at room temperature in glacial acetic acid constitutes a protective method in which the new structures are available with very good yields in some cases.
机译:1,3-双(吲哚-3-基)-四氢环戊[b]吲哚,1,4-双(吲哚-3-基)四氢咔唑,6,10-双(吲哚-3-基)六氢环庚[b]根据本发明开发的通式的6,11-双(吲哚-3-基)六氢环辛基[b]吲哚和11-(吲哚-3-基)苯并[b]咔唑具有选择性抑制作用筛选其他革兰氏阳性和革兰氏阴性细菌和真菌时,金黄色葡萄球菌和耐甲氧西林的金黄色葡萄球菌(MRSA)在较低的微分子浓度范围内的生长情况。在室温下在冰醋酸中由二醛和吲哚生成化合物构成了一种保护性方法,在该方法中,在某些情况下可以以很高的产率获得新结构。

著录项

  • 公开/公告号PL2968271T3

    专利类型

  • 公开/公告日2019-06-28

    原文格式PDF

  • 申请/专利权人 MARTIN-LUTHER-UNIVERSITÄT HALLE-WITTENBERG;

    申请/专利号PL20140722084T

  • 发明设计人 HILGEROTH ANDREAS;

    申请日2014-03-12

  • 分类号A61K31/403;A61K31/404;A61P31/04;C07D209/80;C07D209/86;C07D209/94;

  • 国家 PL

  • 入库时间 2022-08-21 12:01:12

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