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具有抗癌潜力的唑-磺胺类杂合体的最新进展。

Recent development of azole-sulfonamide hybrids with the anticancer potential.

机构信息

Huludao Central Hospital, Huludao, 125000, Liaoning, China.

出版信息

Future Med Chem. 2024;16(12):1267-1281. doi: 10.1080/17568919.2024.2351291. Epub 2024 May 30.

DOI:10.1080/17568919.2024.2351291
PMID:38989985
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11244697/
Abstract

Cancer exhibits heterogeneity that enables adaptability and remains grand challenges for effective treatment. Chemotherapy is a validated and critically important strategy for the treatment of cancer, but the emergence of multidrug resistance which may lead to recurrence of disease or even death is a major hurdle for successful chemotherapy. Azoles and sulfonamides are important anticancer pharmacophores, and azole-sulfonamide hybrids have the potential to simultaneously act on dual/multiple targets in cancer cells, holding great promise to overcome drug resistance. This review outlines the current scenario of azole-sulfonamide hybrids with the anticancer potential, and the structure-activity relationships as well as mechanisms of action are also discussed, covering articles published from 2020 onward.

摘要

癌症表现出的异质性使其具有适应性,仍然是有效治疗的重大挑战。化疗是一种经过验证的、至关重要的癌症治疗策略,但多药耐药的出现可能导致疾病复发甚至死亡,这是化疗成功的主要障碍。唑类和磺胺类是重要的抗癌药效团,唑-磺胺类杂合体有可能同时作用于癌细胞中的双重/多个靶点,有望克服耐药性。本综述概述了具有抗癌潜力的唑-磺胺类杂合体的现状,讨论了构效关系和作用机制,涵盖了 2020 年以来发表的文章。

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J Med Chem. 2023 Aug 10;66(15):10558-10578. doi: 10.1021/acs.jmedchem.3c00721. Epub 2023 Jul 27.
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Cancer chemotherapy and beyond: Current status, drug candidates, associated risks and progress in targeted therapeutics.癌症化疗及其他:当前状况、候选药物、相关风险以及靶向治疗的进展。
Genes Dis. 2022 Mar 18;10(4):1367-1401. doi: 10.1016/j.gendis.2022.02.007. eCollection 2023 Jul.
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Structure-guided identification of novel dual-targeting estrogen receptor α degraders with aromatase inhibitory activity for the treatment of endocrine-resistant breast cancer.基于结构的新型双重靶向雌激素受体 α 降解剂的鉴定及其对治疗内分泌抵抗性乳腺癌的芳香酶抑制活性。
Eur J Med Chem. 2023 May 5;253:115328. doi: 10.1016/j.ejmech.2023.115328. Epub 2023 Apr 6.
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Design, Synthesis, and Biological Evaluation of Sulfonamide Methoxypyridine Derivatives as Novel PI3K/mTOR Dual Inhibitors.新型PI3K/mTOR双重抑制剂——磺酰胺甲氧基吡啶衍生物的设计、合成及生物学评价
Pharmaceuticals (Basel). 2023 Mar 20;16(3):461. doi: 10.3390/ph16030461.
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PLoS One. 2023 Mar 23;18(3):e0283289. doi: 10.1371/journal.pone.0283289. eCollection 2023.
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