Literature DB >> 32187406

The Relation Between Position and Chemical Composition of Bis-Indole Substituents Determines Their Interactions with G-Quadruplex DNA.

Bagineni Prasad1, Rabindra Nath Das1, Jan Jamroskovic2, Rajendra Kumar1, Mattias Hedenström1, Nasim Sabouri2, Erik Chorell1.   

Abstract

G-quadruplex (G4) DNA structures are linked to fundamental biological processes and human diseases, which has triggered the development of compounds that affect these DNA structures. However, more knowledge is needed about how small molecules interact with G4 DNA structures. This study describes the development of a new class of bis-indoles (3,3-diindolyl-methyl derivatives) and detailed studies of how they interact with G4 DNA using orthogonal assays, biophysical techniques, and computational studies. This revealed compounds that strongly bind and stabilize G4 DNA structures, and detailed binding interactions which for example, show that charge variance can play a key role in G4 DNA binding. Furthermore, the structure-activity relationships generated opened the possibilities to replace or introduce new substituents on the core structure, which is of key importance to optimize compound properties or introduce probes to further expand the possibilities of these compounds as tailored research tools to study G4 biology.
© 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.

Entities:  

Keywords:  DNA structures; G-Quadruplexes; bis-indole; drug design; nitrogen heterocycles

Year:  2020        PMID: 32187406     DOI: 10.1002/chem.202000579

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  1 in total

1.  Macrocyclization of bis-indole quinolines for selective stabilization of G-quadruplex DNA structures.

Authors:  Rabindra Nath Das; Måns Andréasson; Rajendra Kumar; Erik Chorell
Journal:  Chem Sci       Date:  2020-09-16       Impact factor: 9.825

  1 in total

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