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易于合成用于 DNA 结合的聚酰胺配体的二聚体。

Facile dimer synthesis for DNA-binding polyamide ligands.

机构信息

Chemimstry Department, University of California, Berkeley, California 94720, USA.

出版信息

Org Lett. 2010 Aug 6;12(15):3488-90. doi: 10.1021/ol1013262.

Abstract

Pyrrole-imidazole polyamide ligands are highly sequence specific synthetic DNA-binding ligands that bind with high affinity. To counter the synthetic difficulties associated with coupling the electron-rich heterocyclic acids to the electron-deficient nucleophilic imidazole amine, a novel approach is described for synthesis of Fmoc-protected dimers for solid-phase peptide synthesis (SPPS). This method produces the dimers in high yields, is broadly applicable to other heterocyclic-containing polyamides, and results in improved ligand yields and synthesis times.

摘要

吡咯并咪唑聚酰胺配体是高度序列特异性的合成 DNA 结合配体,具有高亲和力。为了克服将富电子杂环酸偶联到缺电子亲核咪唑胺时所涉及的合成困难,本文描述了一种用于固相肽合成 (SPPS) 的 Fmoc 保护二聚体的新方法。该方法以高产率得到二聚体,广泛适用于其他含杂环的聚酰胺,并提高了配体的产率和合成时间。

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