Department of Medicinal Chemistry, College of Pharmacy, The University of Florida, Gainesville, FL 32610, USA.
Department of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Molecules. 2023 Jan 9;28(2):677. doi: 10.3390/molecules28020677.
In the past 25 years, a number of efforts have been made toward the development of small molecule interleukin-6 (IL-6) signaling inhibitors, but none have been approved to date. Monosaccharides are a diverse class of bioactive compounds, but thus far have been unexplored as a scaffold for small molecule IL-6-signaling inhibitor design. Therefore, in this present communication, we combined a structure-based drug design approach with carbohydrate building blocks to design and synthesize novel IL-6-signaling inhibitors targeting glycoprotein 130 (gp130). Of this series of compounds, and were the top lead compounds, displaying IC values of 6.9 and 16 µM against SUM159 cell lines, respectively, while still retaining preferential activity against the IL-6-signaling pathway. The carbohydrate moiety was found to improve activity, as -unsubstituted triazole analogues of these compounds were found to be less active in vitro compared to the leads themselves. Thus, and are promising scaffolds for further development and study as IL-6-signaling inhibitors.
在过去的 25 年中,人们做出了许多努力来开发小分子白细胞介素 6(IL-6)信号抑制剂,但迄今为止尚无一种获得批准。单糖是一类具有生物活性的化合物,但迄今为止尚未被探索作为小分子 IL-6 信号抑制剂设计的支架。因此,在本通讯中,我们将基于结构的药物设计方法与碳水化合物构建块相结合,设计并合成了针对糖蛋白 130(gp130)的新型 IL-6 信号抑制剂。在这一系列化合物中, 和 是顶级先导化合物,对 SUM159 细胞系的 IC 值分别为 6.9 和 16µM,同时仍然对 IL-6 信号通路具有优先活性。发现碳水化合物部分可以提高活性,因为与先导化合物本身相比,这些化合物的 -未取代三唑类似物在体外的活性较低。因此, 和 是作为 IL-6 信号抑制剂进一步开发和研究的有前途的支架。