Synthesis of 13H-Benzo[6,7]- and 13H-Benzo[4,5]indolo[3,2-c]- quinolines: A New Series of Potent Specific Ligands for Triplex DNA-Reference-Cited by-同舟云学术

Synthesis of 13H-Benzo[6,7]- and 13H-Benzo[4,5]indolo[3,2-c]- quinolines: A New Series of Potent Specific Ligands for Triplex DNA

Published:1998-03-01 Issue:11 Volume:120 Page:2501-2507
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Nguyen Chi Hung¹,Marchand Christophe¹,Delage Stéphane¹,Sun Jian-Sheng¹,Garestier Thérèse¹,Hélène Claude¹,Bisagni Emile¹

Affiliation:

1. Contribution from the UMR 176 CNRS−Institut Curie, Section Recherche 15 rue Georges Clémenceau, 91405 Orsay, France, and Laboratoire de Biophysique, Muséum National d'Histoire Naturelle INSERM U 201 et CNRS URA 481 43 rue Cuvier, 75231 Paris Cedex 05, France

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja971707x

Reference28 articles.

1. Binding of ethidium bromide to a DNA triple helix. Evidence for intercalation.

2. Intercalation of ethidium bromide into a triple-stranded oligonucleotide

3. Triple Helix-Specific Ligands

4. Characterization of a Triple Helix-specific Ligand

5. Self-association and DNA-binding properties of two triple helix-specific ligands: comparison of a benzo[e]pyridoindole and a benzo[g]pyridoindole

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