• 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

微管蛋白作为一种抗原生动物药物靶点。

Tubulin as an antiprotozoal drug target.

作者信息

Werbovetz Karl A

机构信息

Division of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, Ohio State University, 332 Lloyd M Parks Hall, 500 West 12th Avenue, Columbus, OH 43210, USA.

出版信息

Mini Rev Med Chem. 2002 Dec;2(6):519-29. doi: 10.2174/1389557023405648.

DOI:10.2174/1389557023405648
PMID:12370037
Abstract

Since tubulin is a known anticancer and anthelmintic drug target, the investigation of protozoal tubulin could lead to the development of new antiparasitic drugs. This review outlines the current state of knowledge concerning drug-mammalian tubulin interactions, the effects of antimicrotubule agents on parasites and parasite tubulin, and our current hypotheses regarding the development of selective ligands for protozoal tubulin as antiparasitic drug candidates.

摘要

由于微管蛋白是一种已知的抗癌和抗蠕虫药物靶点,对原生动物微管蛋白的研究可能会促成新型抗寄生虫药物的开发。本综述概述了关于药物与哺乳动物微管蛋白相互作用、抗微管药物对寄生虫和寄生虫微管蛋白的影响,以及我们目前关于开发原生动物微管蛋白选择性配体作为抗寄生虫药物候选物的假说等方面的现有知识状况。

相似文献

1
Tubulin as an antiprotozoal drug target.微管蛋白作为一种抗原生动物药物靶点。
Mini Rev Med Chem. 2002 Dec;2(6):519-29. doi: 10.2174/1389557023405648.
2
Scientific hypothesis: a new strategy for the design of anti-protozoal drugs--DNA polymerase as a drug target.科学假说:抗寄生虫药物设计的新策略——以DNA聚合酶作为药物靶点。
Appl Parasitol. 1994 Sep;35(3):157-68.
3
Polyamine metabolism as chemotherapeutic target in protozoan parasites.多胺代谢作为原生动物寄生虫化疗靶点
Mini Rev Med Chem. 2002 Dec;2(6):553-63. doi: 10.2174/1389557023405549.
4
DNA topoisomerases as targets for antiprotozoal therapy.作为抗寄生虫治疗靶点的DNA拓扑异构酶
Mini Rev Med Chem. 2003 Sep;3(6):597-608. doi: 10.2174/1389557033487863.
5
Targeting polyamines of parasitic protozoa in chemotherapy.化疗中针对寄生原生动物多胺的研究
Trends Parasitol. 2001 May;17(5):242-9. doi: 10.1016/s1471-4922(01)01908-0.
6
Apicidin: a novel antiprotozoal agent that inhibits parasite histone deacetylase.阿皮西丁:一种新型抗寄生虫药,可抑制寄生虫组蛋白脱乙酰酶。
Proc Natl Acad Sci U S A. 1996 Nov 12;93(23):13143-7. doi: 10.1073/pnas.93.23.13143.
7
The acidocalcisome as a target for chemotherapeutic agents in protozoan parasites.酸性钙小体作为原生动物寄生虫化疗药物的靶点。
Curr Pharm Des. 2008;14(9):882-8. doi: 10.2174/138161208784041079.
8
Cellular effects of leishmanial tubulin inhibitors on L. donovani.利什曼原虫微管蛋白抑制剂对杜氏利什曼原虫的细胞效应
Mol Biochem Parasitol. 2000 Oct;110(2):223-36. doi: 10.1016/s0166-6851(00)00272-3.
9
[Target points of antiparasitic drugs].[抗寄生虫药物的靶点]
Wiad Parazytol. 1988;34(4-6):529-43.
10
Mitochondrion of protozoan parasite emerges as potent therapeutic target: exciting drugs are on the horizon.原生动物寄生虫的线粒体成为有力的治疗靶点:令人兴奋的药物即将问世。
Curr Pharm Des. 2008;14(9):839-46. doi: 10.2174/138161208784041024.

引用本文的文献

1
Structure-Activity Relationships, Tolerability and Efficacy of Microtubule-Active 1,2,4-Triazolo[1,5-a]pyrimidines as Potential Candidates to Treat Human African Trypanosomiasis.微管活性 1,2,4-三唑并[1,5-a]嘧啶作为治疗人类非洲锥虫病的潜在候选药物的构效关系、耐受性和疗效。
ChemMedChem. 2023 Oct 17;18(20):e202300193. doi: 10.1002/cmdc.202300193. Epub 2023 Jul 24.
2
What about the Cytoskeletal and Related Proteins of Tapeworms in the Host's Immune Response? An Integrative Overview.绦虫的细胞骨架及相关蛋白在宿主免疫反应中作用如何?综合概述。
Pathogens. 2023 Jun 18;12(6):840. doi: 10.3390/pathogens12060840.
3
Structure-Activity Relationships, Tolerability and Efficacy of Microtubule-Active 1,2,4-Triazolo[1,5- ]pyrimidines as Potential Candidates to Treat Human African Trypanosomiasis.
作为治疗人类非洲锥虫病潜在候选药物的微管活性1,2,4-三唑并[1,5-a]嘧啶的构效关系、耐受性及疗效
bioRxiv. 2023 Mar 11:2023.03.11.532093. doi: 10.1101/2023.03.11.532093.
4
Congeners Derived from Microtubule-Active Phenylpyrimidines Produce a Potent and Long-Lasting Paralysis of In Vitro.源自微管活性苯基嘧啶的同系物在体外可产生强效且持久的麻痹作用。
ACS Infect Dis. 2021 May 14;7(5):1089-1103. doi: 10.1021/acsinfecdis.0c00508. Epub 2020 Oct 31.
5
infection in sheep: Different patterns of virulence and pathogenicity associated with differentially expressed proteomes.绵羊感染:与差异表达蛋白质组相关的不同毒力和致病性模式。
Vet Parasitol X. 2019 Jun 8;2:100014. doi: 10.1016/j.vpoa.2019.100014. eCollection 2019 Nov.
6
An Antiparasitic Compound from the Medicines for Malaria Venture Pathogen Box Promotes Tubulin Polymerization.一种来自疟疾药物研发风险病原体盒的抗寄生虫化合物可促进微管蛋白聚合。
ACS Infect Dis. 2020 Aug 14;6(8):2057-2072. doi: 10.1021/acsinfecdis.0c00122. Epub 2020 Jul 20.
7
Lead optimization of selective tubulin inhibitors as anti-trypanosomal agents.作为抗锥虫药物的选择性微管抑制剂的先导优化。
Bioorg Med Chem. 2019 Apr 15;27(8):1517-1528. doi: 10.1016/j.bmc.2019.02.049. Epub 2019 Feb 25.
8
Recombinant α- and β-tubulin from Echinococcus granulosus: expression, purification and polymerization.细粒棘球绦虫重组α-微管蛋白和β-微管蛋白:表达、纯化及聚合
Parasite. 2018;25:62. doi: 10.1051/parasite/2018063. Epub 2018 Dec 5.
9
Brain-Penetrant Triazolopyrimidine and Phenylpyrimidine Microtubule Stabilizers as Potential Leads to Treat Human African Trypanosomiasis.穿透血脑屏障的三唑并嘧啶和苯嘧啶微管稳定剂可作为治疗人类非洲锥虫病的潜在药物。
ChemMedChem. 2018 Sep 6;13(17):1751-1754. doi: 10.1002/cmdc.201800404. Epub 2018 Aug 7.
10
Synthesis and biological evaluation of selective tubulin inhibitors as anti-trypanosomal agents.作为抗锥虫剂的选择性微管蛋白抑制剂的合成及生物学评价
Bioorg Med Chem. 2017 Jun 15;25(12):3215-3222. doi: 10.1016/j.bmc.2017.04.009. Epub 2017 Apr 8.