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Self-assembled ionophores based on 8-phenyl-2'-deoxyguanosine analogues

Gubala, V., De Jesus, D., Rivera, J.M. (2006) Self-assembled ionophores based on 8-phenyl-2'-deoxyguanosine analogues. Tetrahedron Letters, 47 (9). pp. 1413-1416. ISSN 0040-4039. (doi:10.1016/j.tetlet.2005.12.100) (KAR id:45249)


Novel base-modified G-analogues act as self-assembled ionophores for various metal cations. Their extracting efficiency can be modulated by the presence and substitution pattern of a functionalized phenyl group that replaces the H8 in the guanine base.

Item Type: Article
DOI/Identification number: 10.1016/j.tetlet.2005.12.100
Additional information: Unmapped bibliographic data: LA - English [Field not mapped to EPrints] J2 - Tetrahedron Lett. [Field not mapped to EPrints] AD - Department of Chemistry, University of Puerto Rico, Río Piedras Campus, San Juan 00931, Puerto Rico [Field not mapped to EPrints] DB - Scopus [Field not mapped to EPrints]
Uncontrolled keywords: G-analogues, G-quadruplex, Ionophores, Self-assembly, 8 phenyl 2' deoxyguanosine, guanine, guanosine derivative, ionophore, metal ion, phenyl group, unclassified drug, article, extraction, molecular model, nuclear magnetic resonance spectroscopy
Divisions: Divisions > Division of Natural Sciences > Medway School of Pharmacy
Depositing User: Vladimir Gubala
Date Deposited: 14 Dec 2017 21:40 UTC
Last Modified: 16 Nov 2021 10:18 UTC
Resource URI: (The current URI for this page, for reference purposes)

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