Volume 119, Issue 23 pp. 4384-4387
Zuschrift

Highly Stable Pyrimidine-Motif Triplex Formation at Physiological pH Values by a Bridged Nucleic Acid Analogue

S. M. Abdur Rahman Dr.

S. M. Abdur Rahman Dr.

Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan, Fax: (+81) 6-6879-8204

On leave from the Faculty of Pharmacy, Dhaka University, Dhaka-1000, Bangladesh

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Sayori Seki

Sayori Seki

Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan, Fax: (+81) 6-6879-8204

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Satoshi Obika Dr.

Satoshi Obika Dr.

Graduate School of Pharmaceutical Sciences, Osaka University

PRESTO, JST, 4-1-8 Honcho Kawaguchi, Saitama 332-0012, Japan

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Sunao Haitani

Sunao Haitani

Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan, Fax: (+81) 6-6879-8204

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Kazuyuki Miyashita Prof.

Kazuyuki Miyashita Prof.

Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan, Fax: (+81) 6-6879-8204

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Takeshi Imanishi Prof.

Takeshi Imanishi Prof.

Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan, Fax: (+81) 6-6879-8204

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First published: 24 May 2007
Citations: 2

S.M.A.R. thanks the Japan Society of Promotion of Science (JSPS) for financial support.

Graphical Abstract

Aller guten Dinge sind drei: Eine neuartige überbrückte Nucleinsäure wurde entwickelt, in der die Furanose durch eine sechsgliedrige Brückeneinheit mit einer N-O-Bindung in einer Konformation vom N-Typ fixiert ist (siehe Bild). Oligonucleotide, die aus diesem Rest aufgebaut sind, bilden bei physiologischen pH-Werten stabile Triplexe.

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