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Tri- and tetra-substituted naphthalene diimides as potent G-quadruplex ligands.
Cuenca, Francisco; Greciano, Olga; Gunaratnam, Mekala; Haider, Shozeb; Munnur, Deeksha; Nanjunda, Rupesh; Wilson, W David; Neidle, Stephen.
Afiliação
  • Cuenca F; CRUK Biomolecular Structure Group, The School of Pharmacy, University of London, 29/39 Brunswick Square, London WC1N 1AX, UK.
Bioorg Med Chem Lett ; 18(5): 1668-73, 2008 Mar 01.
Article em En | MEDLINE | ID: mdl-18243701
ABSTRACT
A series of tri- and tetra-substituted naphthalene diimides have been designed and synthesized. Several compounds show exceptional affinity for telomeric G-quadruplex DNA in classical and competition FRET assays and SPR studies. They inhibit telomerase in the TRAP assay, and show potent senescence-based short-term anti-proliferative effects on MCF7 and A549 cancer cell lines, and localize in the nucleus and particularly the nucleolus of MCF7 cells.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenantrolinas / Quadruplex G / Antineoplásicos Idioma: En Ano de publicação: 2008 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenantrolinas / Quadruplex G / Antineoplásicos Idioma: En Ano de publicação: 2008 Tipo de documento: Article