Interactions of cyclic and non-cyclic naphthalene diimide derivatives with different nucleic acids.
Bioorg Med Chem
; 22(9): 2593-601, 2014 May 01.
Article
em En
| MEDLINE
| ID: mdl-24726302
ABSTRACT
Recently, strategy based on stabilization of G-quadruplex telomeric DNA by small organic molecule has been realized by naphthalene diimide derivatives (NDIs). At the same time NDIs bind to DNA duplex as threading intercalators. Here we present cyclic derivative of naphthalene diimide (ligand 1) as DNA-binding ligand with ability to recognition of different structures of telomeric G-quadruplexes and ability to bis-intercalate to double-stranded helixes. The results have been compared to non-cyclic derivative (ligand 2) and revealed that preferential binding of ligands to nucleic acids strongly depends on their topology and structural features of ligands.
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Texto completo:
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Base de dados:
MEDLINE
Assunto principal:
Oligonucleotídeos
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DNA
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Quadruplex G
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Imidas
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Naftalenos
Idioma:
En
Ano de publicação:
2014
Tipo de documento:
Article