The treatment of ulcerative colitis (UC) has been a major medical challenge due to the lack of safe and effective drugs. Molecular hybridization is a promising strategy for the development of drugs with pleiotropic activity, which has been demonstrated in a wide range of diseases. Tofacitinib has exhibited significant effects on the remission of UC, but a series of adverse effects have occurred during its clinical application. Herein, we propose to utilize a molecular hybridization strategy to link tofacitinib with a cytoprotective H(2)S donor (ADTOH) to obtain a series of hybridized molecules ZX-4C~ZX-6C. Among them, ZX-4C exhibited the best performance in the H(2)S release rate and the cytoprotective effects against dextran sulfate sodium (DSS)-induced injury. The in vivo studies showed that ZX-4C could effectively alleviate DSS-induced colitis by enhancing oxidative stress defense and reducing the inflammatory response, demonstrating that it is more potent than the parent drugs. The data from the present study support that this molecular hybridization strategy provides a promising avenue for the treatment of UC.
Discovery of Novel Tofacitinib-ADTOH Molecular Hybridization Derivatives for the Treatment of Ulcerative Colitis.
发现用于治疗溃疡性结肠炎的新型托法替尼-ADTOH分子杂交衍生物
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作者:Mou Yi, Wen Shuai, Wang Yan, Zhao Yao, Li Ying-Ping, Sha Hong-Kai, Gui Li-Juan, Jiang Zheng-Yu, Xu Xiang-Ming
| 期刊: | Antioxidants | 影响因子: | 6.600 |
| 时间: | 2025 | 起止号: | 2025 Mar 8; 14(3):325 |
| doi: | 10.3390/antiox14030325 | 研究方向: | 免疫/内分泌 |
| 疾病类型: | 肠炎 | ||
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