文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
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
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
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 @ 2025

抗利什曼原虫和锥虫药物研发:进展与挑战。

Anti-trypanosomatid drug discovery: progress and challenges.

机构信息

Wellcome Centre for Anti-Infectives Research, Division of Biological Chemistry and Drug Discovery, University of Dundee, Dundee, UK.

出版信息

Nat Rev Microbiol. 2023 Jan;21(1):35-50. doi: 10.1038/s41579-022-00777-y. Epub 2022 Aug 22.


DOI:10.1038/s41579-022-00777-y
PMID:35995950
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9395782/
Abstract

Leishmaniasis (visceral and cutaneous), Chagas disease and human African trypanosomiasis cause substantial death and morbidity, particularly in low- and middle-income countries. Although the situation has improved for human African trypanosomiasis, there remains an urgent need for new medicines to treat leishmaniasis and Chagas disease; the clinical development pipeline is particularly sparse for Chagas disease. In this Review, we describe recent advances in our understanding of the biology of the causative pathogens, particularly from the drug discovery perspective, and we explore the progress that has been made in the development of new drug candidates and the identification of promising molecular targets. We also explore the challenges in developing new clinical candidates and discuss potential solutions to overcome such hurdles.

摘要

利什曼病(内脏利什曼病和皮肤利什曼病)、恰加斯病和非洲人类锥虫病会导致大量死亡和发病,尤其是在中低收入国家。尽管非洲锥虫病的情况有所改善,但仍迫切需要新的药物来治疗利什曼病和恰加斯病;恰加斯病的临床研发管道尤其稀缺。在这篇综述中,我们描述了对病原体生物学的最新理解,特别是从药物发现的角度来看,还探讨了在开发新的候选药物和确定有前途的分子靶标方面取得的进展。我们还探讨了开发新的临床候选药物所面临的挑战,并讨论了克服这些障碍的潜在解决方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4a8/9395782/f89429fd46c9/41579_2022_777_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4a8/9395782/14bd57b38275/41579_2022_777_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4a8/9395782/d47074e63206/41579_2022_777_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4a8/9395782/051c954ee78d/41579_2022_777_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4a8/9395782/f89429fd46c9/41579_2022_777_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4a8/9395782/14bd57b38275/41579_2022_777_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4a8/9395782/d47074e63206/41579_2022_777_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4a8/9395782/051c954ee78d/41579_2022_777_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4a8/9395782/f89429fd46c9/41579_2022_777_Fig4_HTML.jpg

相似文献

[1]
Anti-trypanosomatid drug discovery: progress and challenges.

Nat Rev Microbiol. 2023-1

[2]
Pharmacological approaches to antitrypanosomal chemotherapy.

Mem Inst Oswaldo Cruz. 1999

[3]
Drug discovery for the treatment of leishmaniasis, African sleeping sickness and Chagas disease.

Future Med Chem. 2013-10

[4]
Novel compounds to combat trypanosomatid infections: a medicinal chemical perspective.

Expert Opin Ther Pat. 2011-3-24

[5]
Management of trypanosomiasis and leishmaniasis.

Br Med Bull. 2012-11-7

[6]
Proteasome as a Drug Target in Trypanosomatid Diseases.

Curr Drug Targets. 2023

[7]
Parasite prolyl oligopeptidases and the challenge of designing chemotherapeuticals for Chagas disease, leishmaniasis and African trypanosomiasis.

Curr Med Chem. 2013

[8]
Metallodrugs for the Treatment of Trypanosomatid Diseases: Recent Advances and New Insights.

Curr Pharm Des. 2021

[9]
An Overview on Target-Based Drug Design against Kinetoplastid Protozoan Infections: Human African Trypanosomiasis, Chagas Disease and Leishmaniases.

Molecules. 2021-7-30

[10]
A promising pipeline of preclinical drug candidates for leishmaniasis and chronic Chagas' disease.

Trends Parasitol. 2024-3

引用本文的文献

[1]
Decoding post-transcriptional gene expression controls in trypanosomatids using machine learning.

Wellcome Open Res. 2025-7-9

[2]
Design, Synthesis, and Biological Evaluation of -Acylhydrazones and Their Activity Against Promastigotes.

Microorganisms. 2025-7-2

[3]
High-throughput screening identifies novel chemical scaffolds targeting Leishmania donovani parasites.

World J Microbiol Biotechnol. 2025-7-4

[4]
Discovery of Novel CRK12 Inhibitors for the Treatment of Human African Trypanosomiasis: An Integrated Computational and Experimental Approach.

Pharmaceuticals (Basel). 2025-5-23

[5]
Unraveling Common Patterns and Differences among Cruzipains through Molecular Dynamics Simulations and Structural Analyses.

ACS Omega. 2025-5-2

[6]
Distinct modes of interaction within eIF4F-like complexes and susceptibility to the RocA inhibitor for the Trypanosoma brucei EIF4AI translation initiation factor.

PLoS One. 2025-5-9

[7]
Exploring Lamiaceae diterpenoids as potential multitarget therapeutics for leishmaniasis and chagas disease.

Mol Divers. 2025-4-26

[8]
Allosteric inhibition of trypanosomatid pyruvate kinases by a camelid single-domain antibody.

Elife. 2025-3-31

[9]
The Cyanobacterial Oxadiazine Nocuolin A Shows Broad-Spectrum Toxicity Against Protozoans and the Nematode C. elegans.

Microb Ecol. 2025-3-4

[10]
Zinc from an Essential Element to an Antiparasitic Therapeutic Agent.

ACS Omega. 2025-1-17

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索