Song Jiangli, Chen Hanlian, Pan Rongkai, Jin Fangyu, Tang Jie, Huang Qianqian, Zhou Guohua, Song Xiumei
School of Chemistry & Chemical Engineering, Lingnan Normal University, Cunjin Road 29, Chikan District, Zhanjiang, Guangdong Province 524048, People's Republic of China.
School of Chemistry & Chemical Engineering, Lingnan Normal University, Cunjin Road 29, Chikan District, Zhanjiang, Guangdong Province 524048, People's Republic of China.
Int J Biol Macromol. 2025 Mar;295:139501. doi: 10.1016/j.ijbiomac.2025.139501. Epub 2025 Jan 3.
Understanding the interactions between small molecules and calf thymus deoxyribonucleic acid (ctDNA) is critical for certain aspects of drug discovery. In this study, three 11H-indeno[1,2-b]quinoxalin-11-one thiosemicarbazones were synthesized and their interaction with ctDNA was examined through various spectroscopic techniques, including ultraviolet (UV) spectroscopy, fluorescence spectroscopy, and circular dichroism (CD) spectrum, and through physicochemical methods, including viscosity measurements. In addition, the effects of these thiosemicarbazone compounds 4a, 4b and 4c on several cancer cell lines were explored. The results of UV absorption, fluorescence quenching and CD experiments indicated that compounds 4a, 4b and 4c primarily bound to ctDNA by an intercalation. This mode of interaction was further corroborated by viscosity measurements. Docked poses of compound 4a revealed that it formed a crucial N position hydrogen bond with the DNA receptor. The chemical structure of compound 4a was further confirmed by X-ray crystallographic analysis. Through biological evaluation, it was found that the in vitro cytotoxicity of three compounds agreed with the order of their binding strength to ctDNA, indicating that the antitumor activity of these compounds correlated with their binding affinity to ctDNA.
了解小分子与小牛胸腺脱氧核糖核酸(ctDNA)之间的相互作用对于药物发现的某些方面至关重要。在本研究中,合成了三种11H-茚并[1,2-b]喹喔啉-11-酮硫代半卡巴腙,并通过各种光谱技术,包括紫外(UV)光谱、荧光光谱和圆二色(CD)光谱,以及通过物理化学方法,包括粘度测量,研究了它们与ctDNA的相互作用。此外,还探究了这些硫代半卡巴腙化合物4a、4b和4c对几种癌细胞系的影响。紫外吸收、荧光猝灭和CD实验结果表明,化合物4a、4b和4c主要通过嵌入作用与ctDNA结合。粘度测量进一步证实了这种相互作用模式。化合物4a的对接构象表明它与DNA受体形成了关键的N位氢键。通过X射线晶体学分析进一步证实了化合物4a的化学结构。通过生物学评价发现,三种化合物的体外细胞毒性与其与ctDNA的结合强度顺序一致,表明这些化合物的抗肿瘤活性与其对ctDNA的结合亲和力相关。