Issue 42, 2009
From the journal:

Chemical Communications

G-quadruplex recognition by macrocyclic hexaoxazole (6OTD) dimer: greater selectivity than monomer†

Keisuke Iida,a   Masayuki Tera,a   Takatsugu Hirokawa,b   Kazuo Shin-yac  and  Kazuo Nagasawa*a  

* Corresponding authors

a Department of Biotechnology and Life Science Faculty of Technology, Tokyo University of Agriculture and Technology (TUAT), Koganei, Tokyo 184-8588, Japan
E-mail: knaga@cc.tuat.ac.jp
Fax: +81-42-388-7295
Tel: +81-42-388-7295

b Computational Biology Research Center National Institute of Advanced Industrial Science and Technology, Koto-ku, Tokyo 135-0064, Japan

c Biological Information Research Center National Institute of Advanced Industrial Science and Technology, Koto-ku, Tokyo 135-0064, Japan

Abstract

Macrocyclic hexaoxazole (6OTD) dimers were designed as candidates for potent G-quadruplex binders and synthesized.

Graphical abstract: G-quadruplex recognition by macrocyclic hexaoxazole (6OTD) dimer: greater selectivity than monomer

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Article information

DOI
https://doi.org/10.1039/B910242F
Article type
Communication
Submitted
26 May 2009
Accepted
25 Aug 2009
First published
14 Sep 2009

Chem. Commun., 2009, 6481-6483

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G-quadruplex recognition by macrocyclic hexaoxazole (6OTD) dimer: greater selectivity than monomer

K. Iida, M. Tera, T. Hirokawa, K. Shin-ya and K. Nagasawa, Chem. Commun., 2009, 6481 DOI: 10.1039/B910242F

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