• 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

相似文献

1
New targets for antimalarial drug discovery.抗疟药物发现的新靶标。
Curr Opin Microbiol. 2022 Dec;70:102220. doi: 10.1016/j.mib.2022.102220. Epub 2022 Oct 11.
2
Prioritization of Molecular Targets for Antimalarial Drug Discovery.抗疟药物发现中分子靶标的优先级排序。
ACS Infect Dis. 2021 Oct 8;7(10):2764-2776. doi: 10.1021/acsinfecdis.1c00322. Epub 2021 Sep 15.
3
Efforts Aimed To Reduce Attrition in Antimalarial Drug Discovery: A Systematic Evaluation of the Current Antimalarial Targets Portfolio.旨在减少抗疟药物研发中损耗的努力:对抗疟靶点组合的系统评估
ACS Infect Dis. 2018 Apr 13;4(4):568-576. doi: 10.1021/acsinfecdis.7b00211. Epub 2018 Jan 24.
4
Insights into Integrated Lead Generation and Target Identification in Malaria and Tuberculosis Drug Discovery.疟疾和结核病药物发现中的综合线索生成和靶标鉴定的新见解。
Acc Chem Res. 2017 Jul 18;50(7):1606-1616. doi: 10.1021/acs.accounts.6b00631. Epub 2017 Jun 21.
5
Tackling resistance: emerging antimalarials and new parasite targets in the era of elimination.应对耐药性:消除疟疾时代的新型抗疟药物与新的寄生虫靶点
F1000Res. 2018 Aug 1;7. doi: 10.12688/f1000research.14874.1. eCollection 2018.
6
MalDA, Accelerating Malaria Drug Discovery.疟疾药物研发加速计划(Malaria Drug Discovery Accelerator,简称 MalDA)
Trends Parasitol. 2021 Jun;37(6):493-507. doi: 10.1016/j.pt.2021.01.009. Epub 2021 Feb 26.
7
New horizons in antimalarial drug discovery in the last decade by chemoinformatic approaches.过去十年间通过化学信息学方法进行抗疟药物发现的新进展。
Comb Chem High Throughput Screen. 2015;18(2):129-50. doi: 10.2174/1386207318666141229125155.
8
The antimalarial resistome - finding new drug targets and their modes of action.抗疟耐药组学——寻找新的药物靶点及其作用模式。
Curr Opin Microbiol. 2020 Oct;57:49-55. doi: 10.1016/j.mib.2020.06.004. Epub 2020 Jul 15.
9
The antimalarial pipeline.抗疟药物研发管线。
Curr Opin Pharmacol. 2018 Oct;42:1-6. doi: 10.1016/j.coph.2018.05.006. Epub 2018 May 31.
10
Medicinal Chemistry and Target Identification of Synthetic Clinical and Advanced Preclinical Antimalarial Candidates (2000 - 2022).合成临床及临床前抗疟候选药物(2000 - 2022年)的药物化学与靶点鉴定
Curr Top Med Chem. 2023;23(3):227-247. doi: 10.2174/1568026623666221220140526.

引用本文的文献

1
Combating Malaria: Targeting the Ubiquitin-Proteasome System to Conquer Drug Resistance.抗击疟疾:靶向泛素-蛋白酶体系统以克服耐药性
Trop Med Infect Dis. 2025 Apr 3;10(4):94. doi: 10.3390/tropicalmed10040094.
2
Identification and characterization of thiamine analogs with antiplasmodial activity.具有抗疟原虫活性的硫胺类似物的鉴定与表征
Antimicrob Agents Chemother. 2024 Dec 5;68(12):e0109624. doi: 10.1128/aac.01096-24. Epub 2024 Oct 29.

本文引用的文献

1
Reaction hijacking of tyrosine tRNA synthetase as a new whole-of-life-cycle antimalarial strategy.酪氨酸 tRNA 合成酶的反应劫持作为一种新的全生命周期抗疟策略。
Science. 2022 Jun 3;376(6597):1074-1079. doi: 10.1126/science.abn0611. Epub 2022 Jun 2.
2
Basis for drug selectivity of plasmepsin IX and X inhibition in Plasmodium falciparum and vivax.裂殖体疟原虫和 vivax 中裂殖体蛋白酶 IX 和 X 抑制的药物选择性基础。
Structure. 2022 Jul 7;30(7):947-961.e6. doi: 10.1016/j.str.2022.03.018. Epub 2022 Apr 22.
3
Preclinical characterization and target validation of the antimalarial pantothenamide MMV693183.抗疟泛酰巯基乙胺 MMV693183 的临床前特征描述和靶标验证。
Nat Commun. 2022 Apr 20;13(1):2158. doi: 10.1038/s41467-022-29688-5.
4
Design, Synthesis, and Proof-of-Concept of Triple-Site Inhibitors against Aminoacyl-tRNA Synthetases.设计、合成及三靶点氨酰-tRNA 合成酶抑制剂的概念验证
J Med Chem. 2022 Apr 14;65(7):5800-5820. doi: 10.1021/acs.jmedchem.2c00134. Epub 2022 Apr 1.
5
Double drugging of prolyl-tRNA synthetase provides a new paradigm for anti-infective drug development.双重靶向脯氨酰-tRNA 合成酶为抗感染药物研发提供了新范例。
PLoS Pathog. 2022 Mar 25;18(3):e1010363. doi: 10.1371/journal.ppat.1010363. eCollection 2022 Mar.
6
Acetyl-CoA Synthetase Is Essential for Parasite Intraerythrocytic Development and Chromatin Modification.乙酰辅酶 A 合成酶对于寄生虫的红细胞内发育和染色质修饰是必需的。
ACS Infect Dis. 2021 Dec 10;7(12):3224-3240. doi: 10.1021/acsinfecdis.1c00414. Epub 2021 Nov 12.
7
Design of proteasome inhibitors with oral efficacy in vivo against and selectivity over the human proteasome.设计具有体内抗 和对人蛋白酶体选择性的口服功效的蛋白酶体抑制剂。
Proc Natl Acad Sci U S A. 2021 Sep 28;118(39). doi: 10.1073/pnas.2107213118.
8
Seasonal Malaria Vaccination with or without Seasonal Malaria Chemoprevention.季节性疟疾疫苗接种,无论是否进行季节性疟疾化学预防。
N Engl J Med. 2021 Sep 9;385(11):1005-1017. doi: 10.1056/NEJMoa2026330. Epub 2021 Aug 25.
9
Chemogenomics identifies acetyl-coenzyme A synthetase as a target for malaria treatment and prevention.化学生物基因组学鉴定乙酰辅酶 A 合成酶为疟疾治疗和预防的靶点。
Cell Chem Biol. 2022 Feb 17;29(2):191-201.e8. doi: 10.1016/j.chembiol.2021.07.010. Epub 2021 Aug 3.
10
Repositioning and Characterization of 1-(Pyridin-4-yl)pyrrolidin-2-one Derivatives as Cytoplasmic Prolyl-tRNA Synthetase Inhibitors.1-(吡啶-4-基)吡咯烷-2-酮衍生物作为细胞质脯氨酰-tRNA合成酶抑制剂的重新定位与表征
ACS Infect Dis. 2021 Jun 11;7(6):1680-1689. doi: 10.1021/acsinfecdis.1c00020. Epub 2021 Apr 30.

抗疟药物发现的新靶标。

New targets for antimalarial drug discovery.

机构信息

Department of Pediatrics MC 0760, School of Medicine, University of California, La Jolla, San Diego, CA 92093, USA.

Department of Pediatrics MC 0760, School of Medicine, University of California, La Jolla, San Diego, CA 92093, USA.

出版信息

Curr Opin Microbiol. 2022 Dec;70:102220. doi: 10.1016/j.mib.2022.102220. Epub 2022 Oct 11.

DOI:10.1016/j.mib.2022.102220
PMID:36228458
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9934905/
Abstract

Phenotypic screening methods have placed numerous preclinical candidates into the antimalarial drug-discovery pipeline. As more chemically validated targets become available, efforts are shifting to target-based drug discovery. Here, we briefly review some of the most attractive targets that have been identified in recent years.

摘要

表型筛选方法已经将众多临床前候选药物纳入抗疟药物发现管道。随着更多经过化学验证的靶点的出现,人们的工作重点正在转向基于靶点的药物发现。在这里,我们简要回顾一下近年来发现的一些最有吸引力的靶点。