In this manuscript, we describe a synthetic approach to a novel benzodifuran derivative as well as CD studies regarding its ability to interact with DNA and RNA. After the chemical synthesis and ESI-MS and NMR characterization, this heteroaromatic molecule was investigated by CD spectroscopy in order to evaluate it as a potential nucleic acid binder. Interestingly, the benzodifuran compound was found to be able to induce conformational changes in both DNA and RNA homoadenine molecules forming in the latter case a complex with a 6:1 benzodifuran/nucleobase stoichiometric ratio, as evidenced by CD titration experiments.

Synthesis of a novel benzodifuran derivative and its molecular recognition of poly rA RNA / Roviello, Giovanni N.; Roviello, Valentina; Musumeci, Domenica; Pedone, Carlo. - In: BIOLOGICAL CHEMISTRY. - ISSN 1437-4315. - 394:9(2013), pp. 1235-1239. [10.1515/hsz-2013-0154]

Synthesis of a novel benzodifuran derivative and its molecular recognition of poly rA RNA

Valentina Roviello;MUSUMECI, DOMENICA;PEDONE, CARLO
2013

Abstract

In this manuscript, we describe a synthetic approach to a novel benzodifuran derivative as well as CD studies regarding its ability to interact with DNA and RNA. After the chemical synthesis and ESI-MS and NMR characterization, this heteroaromatic molecule was investigated by CD spectroscopy in order to evaluate it as a potential nucleic acid binder. Interestingly, the benzodifuran compound was found to be able to induce conformational changes in both DNA and RNA homoadenine molecules forming in the latter case a complex with a 6:1 benzodifuran/nucleobase stoichiometric ratio, as evidenced by CD titration experiments.
2013
Synthesis of a novel benzodifuran derivative and its molecular recognition of poly rA RNA / Roviello, Giovanni N.; Roviello, Valentina; Musumeci, Domenica; Pedone, Carlo. - In: BIOLOGICAL CHEMISTRY. - ISSN 1437-4315. - 394:9(2013), pp. 1235-1239. [10.1515/hsz-2013-0154]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/565279
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