The self-assembly of a lipophilic derivative of (5'S)-5',8-cyclo-2'-deoxyguanosine, a mutagenic product formed by hydroxyl radical attack against DNA, has been investigated. This derivative forms, with high fidelity, a dodecameric complex composed of three stacked G-quartets in the presence of strontium picrate. This is the first example of a fully-anti lipophilic G-quadruplex

A lipophilic “fully-anti” dodecamer from a (5'S)-5',8-cyclo-2'-deoxyguanosine / Stefano, Masiero; Silvia, Pieraccini; Chryssostomos, Chatgilialoglu; Michael A., Terzidis; Baldassarri, ENRICO JUNIOR; Giovanna, Fragneto; Mariani, Paolo. - In: CHEMICAL COMMUNICATIONS. - ISSN 1359-7345. - STAMPA. - 50:(2014), pp. 10722-10725. [10.1039/C4CC04275A]

A lipophilic “fully-anti” dodecamer from a (5'S)-5',8-cyclo-2'-deoxyguanosine

BALDASSARRI, ENRICO JUNIOR;MARIANI, Paolo
2014-01-01

Abstract

The self-assembly of a lipophilic derivative of (5'S)-5',8-cyclo-2'-deoxyguanosine, a mutagenic product formed by hydroxyl radical attack against DNA, has been investigated. This derivative forms, with high fidelity, a dodecameric complex composed of three stacked G-quartets in the presence of strontium picrate. This is the first example of a fully-anti lipophilic G-quadruplex
2014
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11566/179709
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 4
  • ???jsp.display-item.citation.isi??? 4
social impact