• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
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
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
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 @ 2026

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

金属药物治疗原生动物病:最新进展和新见解。

Metallodrugs for the Treatment of Trypanosomatid Diseases: Recent Advances and New Insights.

机构信息

Departamento de Quimica, Instituto de Ciencias Exatas, Universidade Federal de Juiz de Fora, Juiz de Fora, Brazil.

Departamento de Química, Instituto de Ciências Exatas, Universidade Federal de Juiz de Fora, Juiz de Fora, Brazil.

出版信息

Curr Pharm Des. 2021;27(15):1763-1789. doi: 10.2174/1381612826666201113104633.

DOI:10.2174/1381612826666201113104633
PMID:33185155
Abstract

Trypanosomatid parasites are responsible for many Neglected Tropical Diseases (NTDs). NTDs are a group of illnesses that prevail in low-income populations, such as in tropical and subtropical areas of Africa, Asia, and the Americas. The three major human diseases caused by trypanosomatids are African trypanosomiasis, Chagas disease and leishmaniasis. There are known drugs for the treatment of these diseases that are used extensively and are affordable; however, the use of these medicines is limited by several drawbacks such as the development of chemo-resistance, side effects such as cardiotoxicity, low selectivity, and others. Therefore, there is a need to develop new chemotherapeutic against these tropical parasitic diseases. Metal-based drugs against NTDs have been discussed over the years as alternative ways to overcome the difficulties presented by approved antiparasitic agents. The study of late transition metal-based drugs as chemotherapeutics is an exciting research field in chemistry, biology, and medicine due to the ability to develop multitarget antiparasitic agents. The evaluation of the late transition metal complexes for the treatment of trypanosomatid diseases is provided here, as well as some insights about their mechanism of action.

摘要

锥虫生物是许多被忽视的热带病(NTDs)的罪魁祸首。NTDs 是一组在低收入人群中流行的疾病,如非洲、亚洲和美洲的热带和亚热带地区。由锥虫引起的三种主要人类疾病是非洲锥虫病、恰加斯病和利什曼病。目前已有针对这些疾病的治疗药物广泛使用且价格实惠;然而,这些药物的使用受到多种因素的限制,如抗药性的发展、心脏毒性等副作用、选择性低等。因此,需要开发针对这些热带寄生虫病的新化疗药物。多年来,金属基药物已被讨论为克服已批准的抗寄生虫药物所带来的困难的替代方法。由于能够开发多靶点抗寄生虫药物,研究后期过渡金属基药物作为化疗药物是化学、生物学和医学领域令人兴奋的研究领域。本文提供了针对锥虫疾病治疗的后期过渡金属配合物的评估,以及关于其作用机制的一些见解。

相似文献

1
Metallodrugs for the Treatment of Trypanosomatid Diseases: Recent Advances and New Insights.金属药物治疗原生动物病:最新进展和新见解。
Curr Pharm Des. 2021;27(15):1763-1789. doi: 10.2174/1381612826666201113104633.
2
Exploring the Potential of Natural Products as Antiparasitic Agents for Neglected Tropical Diseases.探索天然产物作为治疗被忽视热带病的抗寄生虫药物的潜力。
Curr Top Med Chem. 2024;24(2):89-108. doi: 10.2174/0115680266256963230921061925.
3
Organometallic compounds in the discovery of new agents against kinetoplastid-caused diseases.有机金属化合物在发现针对动质体疾病的新药物中的作用。
Eur J Med Chem. 2018 Jul 15;155:459-482. doi: 10.1016/j.ejmech.2018.05.044. Epub 2018 Jun 1.
4
Aminoacyl-tRNA synthetase (AARS) as an attractive drug target in neglected tropical trypanosomatid diseases-Leishmaniasis, Human African Trypanosomiasis and Chagas disease.氨酰-tRNA 合成酶(AARS)作为被忽视的热带利什曼原虫病、非洲人类锥虫病和恰加斯病的一个有吸引力的药物靶点。
Mol Biochem Parasitol. 2022 Sep;251:111510. doi: 10.1016/j.molbiopara.2022.111510. Epub 2022 Aug 18.
5
Small molecules containing chalcogen elements (S, Se, Te) as new warhead to fight neglected tropical diseases.含有硫族元素(硫、硒、碲)的小分子作为对抗被忽视热带病的新型弹头。
Eur J Med Chem. 2023 Jan 15;246:115002. doi: 10.1016/j.ejmech.2022.115002. Epub 2022 Dec 5.
6
Metal Compounds in the Development of Antiparasitic Agents: Rational Design from Basic Chemistry to the Clinic.抗寄生虫药物开发中的金属化合物:从基础化学到临床的合理设计
Met Ions Life Sci. 2019 Jan 14;19. doi: 10.1515/9783110527872-019.
7
Drug discovery for the treatment of leishmaniasis, African sleeping sickness and Chagas disease.治疗利什曼病、非洲昏睡病和恰加斯病的药物发现。
Future Med Chem. 2013 Oct;5(15):1709-18. doi: 10.4155/fmc.13.161.
8
Proteasome as a Drug Target in Trypanosomatid Diseases.蛋白酶体作为一种药物靶点在原生动物疾病中的应用
Curr Drug Targets. 2023;24(10):781-789. doi: 10.2174/1389450124666230719104147.
9
Therapeutic Potential of Flavonoid Derivatives for Certain Neglected Tropical Diseases.类黄酮衍生物在某些被忽视热带病中的治疗潜力。
Curr Drug Targets. 2022;23(7):680-682. doi: 10.2174/1389450123666220309093827.
10
Application of Dithiocarbamates as Potential New Antitrypanosomatids-Drugs: Approach Chemistry, Functional and Biological.二硫代氨基甲酸盐作为潜在新型抗锥虫药物的应用:方法化学、功能和生物学研究。
Molecules. 2019 Aug 1;24(15):2806. doi: 10.3390/molecules24152806.

引用本文的文献

1
Zinc from an Essential Element to an Antiparasitic Therapeutic Agent.从必需元素到抗寄生虫治疗剂的锌。
ACS Omega. 2025 Jan 17;10(3):2393-2414. doi: 10.1021/acsomega.4c07331. eCollection 2025 Jan 28.
2
Metallomics: An Essential Tool for the Study of Potential Antiparasitic Metallodrugs.金属组学:研究潜在抗寄生虫金属药物的重要工具。
ACS Omega. 2024 Mar 25;9(14):15744-15752. doi: 10.1021/acsomega.3c10200. eCollection 2024 Apr 9.
3
The Amoebicidal Activity of Diferrocenyl Derivatives: A Significant Dependence on the Electronic Environment.
二茂铁衍生物的杀变形虫活性:对电子环境有显著依赖性。
Molecules. 2023 Aug 11;28(16):6008. doi: 10.3390/molecules28166008.
4
Zinc(II)-Sterol Hydrazone Complex as a Potent Anti- Agent: Synthesis, Characterization, and Insight into Its Mechanism of Antiparasitic Action.锌(II)-甾醇腙配合物作为一种有效的抗寄生虫剂:合成、表征及其抗寄生虫作用机制的深入研究。
Pharmaceutics. 2023 Mar 31;15(4):1113. doi: 10.3390/pharmaceutics15041113.
5
New Nucleic Base-Tethered Trithiolato-Bridged Dinuclear Ruthenium(II)-Arene Compounds: Synthesis and Antiparasitic Activity.新型核酸碱基连接的三硫醇桥联双核钌(II)-芳基配合物的合成与抗寄生虫活性。
Molecules. 2022 Nov 24;27(23):8173. doi: 10.3390/molecules27238173.
6
Drug Combination Studies of the Dipeptide Nitrile CD24 with Curcumin: A New Strategy to Synergistically Inhibit Rhodesain of .二肽腈 CD24 与姜黄素的联合药物研究:协同抑制. Rhodesain 的新策略
Int J Mol Sci. 2022 Nov 21;23(22):14470. doi: 10.3390/ijms232214470.
7
Development of Urea-Bond-Containing Michael Acceptors as Antitrypanosomal Agents Targeting Rhodesain.含脲键迈克尔受体作为靶向罗得西亚锥虫蛋白酶的抗锥虫剂的开发。
ACS Med Chem Lett. 2022 Jun 30;13(7):1083-1090. doi: 10.1021/acsmedchemlett.2c00084. eCollection 2022 Jul 14.