Suppr超能文献

恶二唑衍生物作为有前景的抗癌药物的二十年综述。

A two-decade overview of oxadiazole derivatives as promising anticancer agents.

作者信息

Salem Mo'men, El-Adl Khaled, El-Morsy Ahmed, Abulkhair Hamada S

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Sinai University-Arish branch Arish Egypt.

Pharmaceutical Chemistry Department, Faculty of Pharmacy, Heliopolis University for Sustainable Development Cairo Egypt

出版信息

RSC Adv. 2025 Sep 10;15(39):32778-32795. doi: 10.1039/d5ra03702f. eCollection 2025 Sep 5.

Abstract

One of the most difficult illnesses that people today must deal with is cancer. It is distinguished by aberrant cell division and growth, which results in the development of tumors and lumps. The heterocyclic nucleus has drawn a lot of interest in the field of chemotherapeutics; moreover, it is essential in medicinal chemistry. Oxadiazole is a nitrogen-oxygen heterocyclic core with five members that exhibits remarkable anticancer properties. Inhibiting different enzymes and growth factors is the mechanism linked to tumor defeat. This review has covered research conducted over the past 20 years as well as their potential applications in drug development as antineoplastic agents, given the significance of oxadiazole and its derivatives in this global panic problem. This review aims to highlight the anticancer properties of 1,3,4-oxadiazole and its derivatives, 1,2,4-oxadiazole.

摘要

当今人们必须应对的最棘手疾病之一就是癌症。它的特征是细胞异常分裂和生长,进而导致肿瘤和肿块的形成。杂环核在化疗领域引起了广泛关注;此外,它在药物化学中也至关重要。恶二唑是一种含五个成员的氮-氧杂环核心,具有显著的抗癌特性。抑制不同的酶和生长因子是与战胜肿瘤相关的机制。鉴于恶二唑及其衍生物在这一全球恐慌问题中的重要性,本综述涵盖了过去20年进行的研究及其作为抗肿瘤药物在药物开发中的潜在应用。本综述旨在突出1,3,4-恶二唑及其衍生物1,2,4-恶二唑的抗癌特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be6d/12422214/8d94de417f67/d5ra03702f-f1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验