文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

用于癌症治疗的秋水仙碱结合位点的双靶抑制剂。

Dual-target inhibitors of colchicine binding site for cancer treatment.

机构信息

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.

出版信息

Eur J Med Chem. 2024 Aug 5;274:116543. doi: 10.1016/j.ejmech.2024.116543. Epub 2024 May 31.


DOI:10.1016/j.ejmech.2024.116543
PMID:38823265
Abstract

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.

摘要

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。

相似文献

[1]
Dual-target inhibitors of colchicine binding site for cancer treatment.

Eur J Med Chem. 2024-8-5

[2]
An overview of tubulin inhibitors that interact with the colchicine binding site.

Pharm Res. 2012-7-20

[3]
Design, synthesis and biological evaluation of a novel tubulin inhibitor 7a3 targeting the colchicine binding site.

Eur J Med Chem. 2018-5-10

[4]
Targeting Tubulin-colchicine Site for Cancer Therapy: Inhibitors, Antibody- Drug Conjugates and Degradation Agents.

Curr Top Med Chem. 2019

[5]
Recent Advances in Heterocyclic Tubulin Inhibitors Targeting the Colchicine Binding Site.

Anticancer Agents Med Chem. 2016

[6]
Novel Natural Product- and Privileged Scaffold-Based Tubulin Inhibitors Targeting the Colchicine Binding Site.

Molecules. 2016-10-15

[7]
Identification and optimization of biphenyl derivatives as novel tubulin inhibitors targeting colchicine-binding site overcoming multidrug resistance.

Eur J Med Chem. 2022-1-15

[8]
Design and synthesis of novel 5-(4-chlorophenyl)furan derivatives with inhibitory activity on tubulin polymerization.

Future Med Chem. 2018-7-3

[9]
Structures of a diverse set of colchicine binding site inhibitors in complex with tubulin provide a rationale for drug discovery.

FEBS J. 2015-11-4

[10]
Recent advances in research of colchicine binding site inhibitors and their interaction modes with tubulin.

Future Med Chem. 2021-5

引用本文的文献

[1]
Microtubule-Targeting Agents: Advances in Tubulin Binding and Small Molecule Therapy for Gliomas and Neurodegenerative Diseases.

Int J Mol Sci. 2025-8-7

[2]
Optimization and Evaluation of Colchicine Patch Formulation Based on Box-Behnken Design.

AAPS PharmSciTech. 2025-7-8

[3]
Case report: Systemic sclerosis during neoadjuvant therapy for breast cancer in a 59-year-old woman.

Front Immunol. 2024-12-13

[4]
Core-Shell Chitosan Particles Targeting Membrane-Bound Heat Shock Protein 70 for Cancer Therapy.

Nanomaterials (Basel). 2024-11-22

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索