Abstract

Phenanthridine derivatives are one of the most intensively studied families of biologically active compounds with efficient DNA binding capability. Attracting attention since DNA structure discovery (1960s), they were early recognized as a symbol of DNA intercalative binding, for many decades applied as gold-standard DNA- and RNA-fluorescent markers (ethidium bromide), probes for cell viability (propidium iodide), but also “ill-famed” for various toxic (genotoxic) and mutagenic effects. After two decades of low interest, the discovery of phenanthridine alkaloids and new studies of antiparasitic/antitumor properties of phenanthridine derivatives resulted in the strong increase of the scientific interest about the turn of this century. Here are summarized phenanthridine-related advances in the 21st century (2000-present period) with emphasis on the supramolecular interactions and bioorganic chemistry, as well as novel or improved synthetic approaches.

Highlights

  • The search for therapeutic agents of the phenanthridine type has increased when the outstanding trypanocidal activity of some phenanthridinium compounds became apparent [1]

  • One of the most studied and used phenanthridine derivatives is 3,8diamino-5-ethyl-6-phenylphenanthridinium known as ethidium bromide (EB), for many decades applied as gold-standard DNA- and RNA-fluorescent marker, and its close analogue as a probe for cell viability

  • Discovery of phenanthridine alkaloid analogues and in parallel new studies of antiparasitic properties of phenanthridine derivatives resulted in a strong increase of the scientific

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Summary

Introduction

The search for therapeutic agents of the phenanthridine type has increased when the outstanding trypanocidal activity of some phenanthridinium compounds became apparent [1]. The method is limited to ortho-substituted aryl iodides as starting material and requires a convenient imine derivative allowing the cleavage of the nitrogen-attached group (R5) at Scheme 11: The common Pd-catalyst for the biphenyl conjugation results simultaneously in picolinamide-directed cyclisation; obtained N-picolinamide dihydrophenanthridine is converted to phenanthridine [32].

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