Current Medicinal Chemistry

Atta-ur-Rahman, FRS
Honorary Life Fellow
Kings College
University of Cambridge


Backbone Modification of Nucleic Acids: Synthesis, Structure and Therapeutic Applications

Author(s): Jason Micklefield.


Nucleic acids have been extensively modified by replacing the phosphodiester group or the whole sugar-phosphodiester backbone with alternative anionic, neutral and cationic structures. Several of these modified oligonucleotides exhibit improved properties including enhanced recognition and binding to RNA, duplex DNA and proteins. This has resulted in the development of new and more potent antisense and antigene agents, as well as aptamers. Furthermore, backbone modified oligonucleotides have also been used in the development of several alternative strategies, which rely on altogether different mechanisms of action and show significant promise for therapeutic intervention. In this review the latest advances in the synthesis and evaluation of the most promising backbone modified oligos will be discussed, with a view to their future as novel pharmaceuticals.

Keywords: Nucleic Acids Synthesis, potent antisense, antigene agents, aptamers, Therapeutic Targets, Phosphoramidate Modification, Boranophosphate Oligos, Methylphosophonates, Deoxyribonucleic Guanidine (DNG) Oligos, Morpholino Oligos

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Article Details

Year: 2001
Page: [1157 - 1179]
Pages: 23
DOI: 10.2174/0929867013372391
Price: $58