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Titlebook: Development of Selective DNA-Interacting Ligands; Understanding the Fu Sefan Asamitsu Book 2020 The Editor(s) (if applicable) and The Autho

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书目名称Development of Selective DNA-Interacting Ligands
副标题Understanding the Fu
编辑Sefan Asamitsu
视频video
概述Nominated as an outstanding Ph.D. thesis by Kyoto University.Includes systematic and exhaustive reviews of non-canonical DNA structures.Offers extensive information on the synthesis of molecules, in a
丛书名称Springer Theses
图书封面Titlebook: Development of Selective DNA-Interacting Ligands; Understanding the Fu Sefan Asamitsu Book 2020 The Editor(s) (if applicable) and The Autho
描述This book addresses the development of both DNA-sequence-selective and DNA-form-selective ligands, with the aim of creating potential molecular probes and therapeutic agents for non-canonical DNA structure-caused human diseases.  .Over the past two decades, the structural diversity of DNA forms has been proven to have profound implications in various biological, neurological, and pharmacological events. In response, researchers have since made tremendous efforts to obtain highly active drugs interacting with disease-related non-canonical DNA structures. These drugs, however, have not yet been approved for clinical use. One obstacle impeding their clinical application has to do with selectivity.   .This book focuses on secondary DNA structures formed by trinucleotide repeat sequences (“hairpin form”) or guanine-rich sequences (“G-quadruplex form”), both of which are pathological molecules for neurodegenerative diseases and/or cancer. Most importantly, it contends that a particular secondary structure of DNA in the context of the human genome can be targeted with a minimal affinity to other DNA structures by means ofcareful and rational ligand design. This approach opens an avenue to
出版日期Book 2020
关键词Non-canonical DNA Structure; Trinucleotide Repeat; G-quadruplex; Synthetic Ligand; Rational Ligand Desig
版次1
doihttps://doi.org/10.1007/978-981-15-7716-1
isbn_softcover978-981-15-7718-5
isbn_ebook978-981-15-7716-1Series ISSN 2190-5053 Series E-ISSN 2190-5061
issn_series 2190-5053
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Singapor
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,Sequence-Specific DNA Alkylation and Transcriptional Inhibition by Long-Chain Hairpin Pyrrole–Imidabucil (Chl) conjugates targeted to CAG/CTG repeat sequences that are associated with trinucleotide repeat disorders. A high-resolution denaturing polyacrylamide sequencing gel analysis revealed sequence-specific alkylations by PI polyamide-Chl conjugates at the N3 of adenines or guanines in CAG/CTG
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Ligand-Mediated G-Quadruplex Induction in a Double-Stranded DNA Context by Cyclic Imidazole/Lysine ological events. Therefore, G4 ligands have attracted great attention as potential anticancer therapies or in molecular probe applications. Here, we designed cyclic imidazole/lysine polyamide (cIKP) as a new class of G4 ligand. It was readily synthesized without time-consuming column chromatography.
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Grundlagen der Tektonik und Strukturgeologiece plasmon resonance (SPR), and NMR techniques, we showed the dual and simultaneous recognition of the respective segment via hybrid molecules, and the synergistic and mutual effect of each binding component that was appropriately linked on higher binding affinity and modest sequence specificity. Mo
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Book 2020 and therapeutic agents for non-canonical DNA structure-caused human diseases.  .Over the past two decades, the structural diversity of DNA forms has been proven to have profound implications in various biological, neurological, and pharmacological events. In response, researchers have since made tr
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