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DC Field | Value | Language |
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dc.contributor.author | Wirote Tuntiwechapikul | en_US |
dc.contributor.author | Thanachai Taka | en_US |
dc.contributor.author | Mathilde Béthencourt | en_US |
dc.contributor.author | Luksana Makonkawkeyoon | en_US |
dc.contributor.author | T. Randall Lee | en_US |
dc.date.accessioned | 2018-09-11T08:54:27Z | - |
dc.date.available | 2018-09-11T08:54:27Z | - |
dc.date.issued | 2006-08-01 | en_US |
dc.identifier.issn | 0960894X | en_US |
dc.identifier.other | 2-s2.0-33745141952 | en_US |
dc.identifier.other | 10.1016/j.bmcl.2006.04.078 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33745141952&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/61512 | - |
dc.description.abstract | Three 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.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
dc.title | The influence of pH on the G-quadruplex binding selectivity of perylene derivatives | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Bioorganic and Medicinal Chemistry Letters | en_US |
article.volume | 16 | en_US |
article.stream.affiliations | Faculty of Medicine, Chiang Mai University | en_US |
article.stream.affiliations | University of Houston | en_US |
Appears in Collections: | CMUL: Journal Articles |
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