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2000
Volume 7, Issue 3
  • ISSN: 1389-5575
  • E-ISSN: 1875-5607

Abstract

Novel compounds have been developed that (in many cases) inhibit cholinesterases and concomitantly interact with at least one further pharmacological target, such as 5-HT3 or H3 receptors. But also enzymes like monoamine oxidase and the serotonin transporter have been targeted. Hybrid molecules can also incorporate antioxidant or neuronal Ca2+- channel-blocking structures.

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/content/journals/mrmc/10.2174/138955707780059817
2007-03-01
2025-06-26
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