Insight into Structure-Activity Relationship of New Compounds for Breast Cancer Treatment

乳腺癌 药效团 表观遗传学 癌症 医学 计算生物学 癌症研究 化学 生物信息学 生物 内科学 生物化学 基因
作者
Lu Li,Qiangsheng Zhang
出处
期刊:Current Topics in Medicinal Chemistry [Bentham Science]
卷期号:23 (25): 2373-2393 被引量:1
标识
DOI:10.2174/0115680266253686230921054429
摘要

Background: Breast cancer has always been a vicious disease that threatens female health. Although the existing surgery, radiotherapy, chemotherapy, and kinase-targeted drugs have achieved certain effects, there are still many shortcomings. Novel compounds used to treat breast cancer, particularly TNBC, are eagerly being discovered. Methods: More than 100 novel compounds that show anti-breast cancer growth were compiled from public databases. The compound design strategies, structure-activity relationship research, and activity evaluation methods have also been reviewed. Results: These novel anti-breast cancer compounds can be divided into mechanisms of action: kinase inhibitors, epigenetic inhibitors, dual inhibitors, degraders, metal complexes, etc. The design strategies mainly include conformational constraint, scaffold-hopping, merging key pharmacophores, etc. Structure-activity relationship studies of these new compounds mainly focus on increasing activity, improving selectivity, increasing membrane permeability, reducing toxicity, improving pharmacokinetic properties, etc. Conclusion: Through the structural optimization of kinase inhibitors, microtubule-targeted drugs, and metal complexes, it is expected to obtain more advantageous breast cancer treatment drugs. It cannot be ignored that epigenetic inhibitors, dual inhibitors and degraders may bring new breast cancer treatment strategies.
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