4.5 Review

G-Quadruplex Binding Ligands: from Naturally Occurring to Rationally Designed Molecules

期刊

CURRENT PHARMACEUTICAL DESIGN
卷 18, 期 14, 页码 1948-1972

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/138161212799958431

关键词

DNA G-quadruplex; RNA G-quadruplex; telomere; oncogene promoter G-quadruplex; telomeric RNA

资金

  1. National Research Foundation of Korea (NRF)
  2. Ministry of Education, Science, and Technology [2008-0060771, 2010-0029358]
  3. National Research Foundation of Korea [2010-0029358, 2008-0060771] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Guanine-rich nucleic acid sequences are known to form G-quadruplex -four-stranded DNA or RNA structures stabilized by an array of Hoogsteen hydrogen bonds. G-quadruplex structures are involved in the modulation of gene expression at the transcription and translation levels. Accordingly, G-quadruplexes are considered as novel therapeutic targets for anticancer drug development. In this review, the authors provide a brief, up-to-date summary of G-quadruplex binding ligands, including naturally occurring molecules, synthetic compounds, and molecules identified by computational database screening. The key structural motifs of G-quadruplex binding ligands, that is, an aromatic core and basic side chains, are addressed in the context of how these molecules interact with G-quadruplex. A better understanding of these interactions would facilitate the rational design of ligands selective for DNA or RNA G-quadruplex.

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