Gubala, V., Rivera-Sanchez, M.C., Hobley, G., Rivera, J.M. (2007) The impact of 8-aryl-and 8-heteroaryl-2'-deoxyguanosine derivatives on G-quadruplex formation. Nucleic acids symposium series, 51 (1). pp. 39-40. ISSN 1746-8272. (doi:10.1093/nass/nrm020) (KAR id:45248)
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Official URL: https://doi.org/10.1093/nass/nrm020 |
Abstract
Guanine and G-rich oligonucleotides are known to self-assemble in the presence of a variety of cations to form higher ordered structures known as Gquadruplexes. We have synthesized a library of 8-aryl/heteroaryl-2'-deoxyguanosine derivatives (8ArGs) that are also able to self-assemble into quadruplex structures. We demonstrate that the properties of such quadruplexes can be modulated by the nature of the groups attached to the guanine base. These supramolecules are potentially useful in the development of self-assembled nanodevices.
Item Type: | Article |
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DOI/Identification number: | 10.1093/nass/nrm020 |
Additional information: | Unmapped bibliographic data: LA - English [Field not mapped to EPrints] J2 - Nucleic Acids Symp Ser (Oxf) [Field not mapped to EPrints] C2 - 18029575 [Field not mapped to EPrints] AD - Department of Chemistry, University of Puerto Rico, RÃo Piedras Campus, PO Box 23346, San Juan, Puerto Rico, 00931, USA. [Field not mapped to EPrints] DB - Scopus [Field not mapped to EPrints] |
Uncontrolled keywords: | deoxyguanosine, drug derivative, guanine quadruplex, nanomaterial, potassium, unclassified drug, article, chemistry, nuclear magnetic resonance, Deoxyguanosine, G-Quadruplexes, Nanostructures, Nuclear Magnetic Resonance, Biomolecular, Potassium |
Divisions: | Divisions > Division of Natural Sciences > Medway School of Pharmacy |
Depositing User: | Vladimir Gubala |
Date Deposited: | 14 Dec 2017 21:36 UTC |
Last Modified: | 05 Nov 2024 10:29 UTC |
Resource URI: | https://kar.kent.ac.uk/id/eprint/45248 (The current URI for this page, for reference purposes) |
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