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二聚体2-氨基-1,8-萘啶及相关DNA结合分子的合成。

Synthesis of dimeric 2-amino-1,8-naphthyridine and related DNA-binding molecules.

作者信息

Nakatani Kazuhiko, He Hanping, Uno Shin-Nosuke, Yamamoto Tsuyoshi, Dohno Chikara

机构信息

Osaka University, Ibaraki, Japan.

出版信息

Curr Protoc Nucleic Acid Chem. 2008 Mar;Chapter 8:Unit 8.6. doi: 10.1002/0471142700.nc0806s32.

Abstract

The synthetic protocols for dimeric 2-amino-1,8-naphthyridine and related compounds are described in this unit. These compounds represent a novel class of compounds that bind selectively to mismatched base pairs. The compounds consist of two main components: the heterocycles and a linker. Connecting two heterocycles by a linker was found to modulate the binding selectivity. This unit describes the synthesis of dimeric 2-amino-1,8-naphthyridine (which binds to the G-G mismatch), naphthyridine-azaquinolone (for the G-A mismatch), N-alkyl naphthyridine dimer (for the C-C mismatch), and naphthyridine carbamate dimer (for G-G mismatches in the (CGG)(n) trinucleotide repeat). Protocols for connecting the short linker to these molecules providing the compounds suitable for immobilization on solid surface are also described.

摘要

本单元介绍了二聚体2-氨基-1,8-萘啶及相关化合物的合成方案。这些化合物代表了一类新型化合物,它们能选择性地与错配碱基对结合。这些化合物由两个主要成分组成:杂环和连接体。研究发现,通过连接体连接两个杂环可调节结合选择性。本单元描述了二聚体2-氨基-1,8-萘啶(与G-G错配结合)、萘啶-氮杂喹诺酮(用于G-A错配)、N-烷基萘啶二聚体(用于C-C错配)和萘啶氨基甲酸酯二聚体(用于(CGG)(n)三核苷酸重复序列中的G-G错配)的合成。还介绍了将短连接体连接到这些分子上以提供适合固定在固体表面的化合物的方案。

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