Das Rabindra Nath, Andréasson Måns, Kumar Rajendra, Chorell Erik
Department of Chemistry, Umeå University 90187 Umeå Sweden
Chem Sci. 2020 Sep 16;11(38):10529-10537. doi: 10.1039/d0sc03519j.
The recognition of G-quadruplex (G4) DNA structures as important regulatory elements in biological mechanisms, and the connection between G4s and the evolvement of different diseases, has sparked interest in developing small organic molecules targeting G4s. However, such compounds often lack drug-like properties and selectivity. Here, we describe the design and synthesis of a novel class of macrocyclic bis-indole quinolines based on their non-macrocyclic lead compounds. The effects of the macrocyclization on the ability to interact with G4 DNA structures were investigated using biophysical assays and molecular dynamic simulations. Overall, this revealed compounds with potent abilities to interact with and stabilize G4 structures and a clear selectivity for both G4 DNA over dsDNA and for parallel/hybrid G4 topologies, which could be attributed to the macrocyclic structure. Moreover, we obtained knowledge about the structure-activity relationship of importance for the macrocyclic design and how structural modifications could be made to construct improved macrocyclic compounds. Thus, the macrocyclization of G4 ligands can serve as a basis for the optimization of research tools to study G4 biology and potential therapeutics targeting G4-related diseases.
G-四链体(G4)DNA结构作为生物机制中的重要调控元件被认识,以及G4与不同疾病演变之间的联系,引发了人们对开发靶向G4的小分子有机化合物的兴趣。然而,这类化合物往往缺乏类药物性质和选择性。在此,我们描述了基于其非大环先导化合物设计和合成的一类新型大环双吲哚喹啉。使用生物物理测定法和分子动力学模拟研究了大环化对与G4 DNA结构相互作用能力的影响。总体而言,这揭示了具有与G4结构相互作用并使其稳定的强大能力的化合物,以及对G4 DNA比对双链DNA以及对平行/杂合G4拓扑结构具有明显选择性,这可归因于大环结构。此外,我们获得了对于大环设计重要的构效关系知识,以及如何进行结构修饰以构建改进的大环化合物。因此,G4配体的大环化可作为优化研究工具以研究G4生物学和靶向G4相关疾病的潜在疗法的基础。