5-Substituted 2-Aminopyridine C-Nucleosides as Protonated Cytidine Equivalents: Increasing Efficiency and Selectivity in DNA Triple-Helix Formation
- 1 June 1997
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (24) , 5499-5511
- https://doi.org/10.1021/ja9704904
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Erhöhung der Stabilität von DNA‐Tripelhelices bei neutralem pH durch Verwendung von Oligonucleotiden mit einem basischeren Desoxycytidin‐AnalogonAngewandte Chemie, 1996
- Syntheses of Two Pyridine C-Nucleosides as "Deletion-Modified" Analogs of dT and dCThe Journal of Organic Chemistry, 1995
- Synthesis of 6-amino-2′--methylcytidine, a protonated cytidine analog for triple helix binding studiesBioorganic & Medicinal Chemistry Letters, 1994
- Sequenzspezifische Erkennung und Modifikation von Doppelhelix‐DNA durch OligonucleotideAngewandte Chemie, 1993
- Triple-helix formation by oligodeoxynucleotides containing the carbocyclic analogs of thymidine and 5-methyl-2'-deoxycytidineJournal of the American Chemical Society, 1992
- Oligo(2′‐O‐methyl)ribonucleotides Effective probes for duplex DNAFEBS Letters, 1992
- Synthesis and cytotoxic activity of C-glycosidic nicotinamide riboside analogsJournal of Medicinal Chemistry, 1992
- Excited-state properties in supramolecular systems. Luminescence and intercomponent interactions in a 3-catenand and some 3-catenatesJournal of the American Chemical Society, 1991
- A Direct Route to 3‐(D‐Ribofuranosyl)pyridine NucleosidesHelvetica Chimica Acta, 1991
- FORMATION OF A THREE-STRANDED POLYNUCLEOTIDE MOLECULEJournal of the American Chemical Society, 1957