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dc.contributor.authorWirote Tuntiwechapikulen_US
dc.contributor.authorThanachai Takaen_US
dc.contributor.authorMathilde Béthencourten_US
dc.contributor.authorLuksana Makonkawkeyoonen_US
dc.contributor.authorT. Randall Leeen_US
dc.description.abstractThree new perylene derivatives with branched ionizable side chains were synthesized, and their G-quadruplex binding specificities were compared by spectroscopic and electrophoretic analysis with two well-studied G-quadruplex ligands: PIPER and TmPyP4. The value of pH and consequent charge formation and self-aggregation of these perylene derivatives influences not only the type of G-quadruplex formation, but also the G-quadruplex binding selectivity. © 2006 Elsevier Ltd. All rights reserved.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleThe influence of pH on the G-quadruplex binding selectivity of perylene derivativesen_US
article.title.sourcetitleBioorganic and Medicinal Chemistry Lettersen_US
article.volume16en_US of Medicine, Chiang Mai Universityen_US of Houstonen_US
Appears in Collections:CMUL: Journal Articles

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