Henan Key Laboratory of Natural Medicine Innovation and Transformation, Henan University, Kaifeng, Henan Province, 475004, China.
Translational Medicine Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, 450052, China.
Eur J Med Chem. 2024 Aug 5;274:116543. doi: 10.1016/j.ejmech.2024.116543. Epub 2024 May 31.
Colchicine binding site inhibitors (CBSIs) have attracted much attention due to their antitumor efficacies and the advantages of inhibiting angiogenesis and overcoming multidrug resistance. However, no CBSI has been currently approved for cancer treatment due to the insufficient efficacies, serious toxicities and poor pharmacokinetic properties. Design of dual-target inhibitors is becoming a potential strategy for cancer treatment to improve anticancer efficacy, decrease adverse events and overcome drug resistance. Therefore, we reviewed dual-target inhibitors of colchicine binding site (CBS), summarized the design strategies and the biological activities of these dual-target inhibitors, expecting to provide inspiration for developing novel dual inhibitors based on CBS.
秋水仙碱结合位点抑制剂(CBSIs)由于其抗肿瘤功效以及抑制血管生成和克服多药耐药性的优势而受到广泛关注。然而,由于疗效不足、毒性严重和药代动力学性质差,目前尚无 CBSI 被批准用于癌症治疗。设计双重靶标抑制剂正在成为癌症治疗的一种潜在策略,以提高抗癌疗效、减少不良反应和克服耐药性。因此,我们综述了秋水仙碱结合位点(CBS)的双重靶标抑制剂,总结了这些双重靶标抑制剂的设计策略和生物学活性,期望为基于 CBS 开发新型双重抑制剂提供启示。
Eur J Med Chem. 2024-8-5
Anticancer Agents Med Chem. 2016
AAPS PharmSciTech. 2025-7-8
Front Immunol. 2024-12-13
Nanomaterials (Basel). 2024-11-22