Studies on anti-Helicobacter pylori agents. Part 1: Benzyloxyisoquinoline derivatives

Bioorg Med Chem. 1999 Nov;7(11):2647-66. doi: 10.1016/s0968-0896(99)00203-5.

Abstract

The synthesis and optimization of the anti-Helicobacter pylori activity of a novel series of benzyloxyisoquinoline derivatives that was discovered by a random screening process, are described. In the in vitro assay, compound 10c containing a 3-acetamido-2,6-dichlorobenzyl substituent was found to have extremely potent activity against H. pylori and no activity against other common bacteria. The anti-H. pylori activity of 10c was superior to that of amoxicillin (AMPC) (1) and clarithromycin (CAM) (2). However, 10c did not show in vivo efficacy in a mouse infection model; a feature attributed to the lack of strong bactericidal activity at short contact times.

MeSH terms

  • Amoxicillin / pharmacology
  • Animals
  • Anti-Bacterial Agents / chemical synthesis
  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / pharmacology*
  • Anti-Bacterial Agents / therapeutic use
  • Disease Models, Animal
  • Helicobacter Infections / drug therapy
  • Helicobacter pylori / drug effects*
  • Helicobacter pylori / physiology
  • Isoquinolines / chemical synthesis*
  • Isoquinolines / chemistry
  • Isoquinolines / pharmacology
  • Mice
  • Mice, Inbred ICR
  • Microbial Sensitivity Tests
  • Penicillins / pharmacology
  • Structure-Activity Relationship

Substances

  • Anti-Bacterial Agents
  • Isoquinolines
  • Penicillins
  • Amoxicillin