• 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

抗疟药物发现和开发的最新技术。

The state of the art in anti-malarial drug discovery and development.

机构信息

Medicines for Malaria Venture, ICC, Geneva, Switzerland.

出版信息

Curr Top Med Chem. 2011;11(10):1226-54. doi: 10.2174/156802611795429194.

DOI:10.2174/156802611795429194
PMID:21401508
Abstract

Malaria is one of the most prevalent and devastating infectious diseases of our time. Yet, unfortunately, apart from artemisinin combination therapies there are relatively few effective treatments for Plasmodium falciparum and only one treatment for the radical cure of Plasmodium vivax. Novel classes of antimalarial medicines are urgently needed given the long-term inevitability of resistance to current therapies and the need for drugs that are well tolerated by all. This review summarises the antimalarials developed and registered thus far, as well as describing some of the new small molecule therapy approaches being developed as a contribution towards the malaria eradication agenda.

摘要

疟疾是我们这个时代最流行和最具破坏性的传染病之一。然而,不幸的是,除了青蒿素联合疗法外,针对恶性疟原虫和间日疟原虫根治的有效治疗方法相对较少。鉴于当前疗法的耐药性不可避免且需要所有患者都能耐受的药物,迫切需要新型抗疟药物。本综述总结了迄今为止开发和注册的抗疟药物,并描述了一些正在开发的新的小分子治疗方法,为消除疟疾议程做出贡献。

相似文献

1
The state of the art in anti-malarial drug discovery and development.抗疟药物发现和开发的最新技术。
Curr Top Med Chem. 2011;11(10):1226-54. doi: 10.2174/156802611795429194.
2
Malaria chemotherapy: recent advances in drug development.疟疾化疗:药物研发的最新进展
Recent Pat Antiinfect Drug Discov. 2010 Nov;5(3):195-225. doi: 10.2174/157489110793348776.
3
Natural products as starting points for future anti-malarial therapies: going back to our roots?天然产物作为未来抗疟疗法的起点:回归本源?
Malar J. 2011 Mar 15;10 Suppl 1(Suppl 1):S3. doi: 10.1186/1475-2875-10-S1-S3.
4
Recent progress in the identification and development of anti-malarial agents using virtual screening based approaches.基于虚拟筛选方法的抗疟药物鉴定与开发的最新进展。
Comb Chem High Throughput Screen. 2015;18(3):257-68. doi: 10.2174/1386207318666150305154913.
5
Susceptibility of Plasmodium falciparum to artemisinins and Plasmodium vivax to chloroquine in Phuoc Chien Commune, Ninh Thuan Province, south-central Vietnam.越南中南部宁顺省福川乡恶性疟原虫对青蒿素类药物的敏感性和间日疟原虫对氯喹的敏感性。
Malar J. 2019 Jan 17;18(1):10. doi: 10.1186/s12936-019-2640-2.
6
Hits, leads and drugs against malaria through diversity-oriented synthesis.通过多样性导向合成寻找、引导和研发疟疾药物。
Future Med Chem. 2012 Dec;4(18):2279-94. doi: 10.4155/fmc.12.178.
7
Artemisinin derivatives and malaria: useful, in combination with other antimalarials.青蒿素衍生物与疟疾:与其他抗疟药物联合使用时有效。
Prescrire Int. 2008 Aug;17(96):162-8.
8
Artemisinin-naphthoquine for treating uncomplicated Plasmodium falciparum malaria.青蒿素-萘酚喹治疗非复杂性恶性疟原虫疟疾
Cochrane Database Syst Rev. 2015 Feb 23;2015(2):CD011547. doi: 10.1002/14651858.CD011547.
9
Antimalarial activity of 4-amidinoquinoline and 10-amidinobenzonaphthyridine derivatives.4-脒基喹啉和10-脒基苯并萘啶衍生物的抗疟活性。
J Med Chem. 2015 Apr 23;58(8):3411-31. doi: 10.1021/jm501809x. Epub 2015 Apr 9.
10
Quinoline--a promising fragment in the search for new antimalarials.喹啉——寻找新型抗疟药物过程中一个有前景的片段。
Mini Rev Med Chem. 2014 Apr;14(4):332-44. doi: 10.2174/1389557514666140220123226.

引用本文的文献

1
The Importance of Murine Models in Determining In Vivo Pharmacokinetics, Safety, and Efficacy in Antimalarial Drug Discovery.小鼠模型在抗疟药物发现中确定体内药代动力学、安全性和疗效方面的重要性。
Pharmaceuticals (Basel). 2025 Mar 18;18(3):424. doi: 10.3390/ph18030424.
2
Therapeutic Approaches for Non-Melanoma Skin Cancer: Standard of Care and Emerging Modalities.非黑色素瘤皮肤癌的治疗方法:标准护理和新兴疗法。
Int J Mol Sci. 2024 Jun 27;25(13):7056. doi: 10.3390/ijms25137056.
3
Revisiting drug-protein interaction prediction: a novel global-local perspective.
重新审视药物-蛋白质相互作用预测:一种新颖的全局-局部视角。
Bioinformatics. 2024 May 2;40(5). doi: 10.1093/bioinformatics/btae271.
4
Vitamin D receptor (VDR) on the cell membrane of mouse macrophages participates in the formation of lipopolysaccharide tolerance: mVDR is related to the effect of artesunate to reverse LPS tolerance.鼠巨噬细胞膜上的维生素 D 受体 (VDR) 参与脂多糖耐受的形成:mVDR 与青蒿琥酯逆转 LPS 耐受的作用有关。
Cell Commun Signal. 2023 May 29;21(1):124. doi: 10.1186/s12964-023-01137-w.
5
Artesunate interacts with the vitamin D receptor to reverse sepsis-induced immunosuppression in a mouse model via enhancing autophagy.青蒿琥酯通过增强自噬与维生素 D 受体相互作用,逆转脓毒症诱导的小鼠模型中的免疫抑制。
Br J Pharmacol. 2020 Sep;177(18):4147-4165. doi: 10.1111/bph.15158. Epub 2020 Jul 6.
6
Artesunate Affects T Antigen Expression and Survival of Virus-Positive Merkel Cell Carcinoma.青蒿琥酯影响病毒阳性默克尔细胞癌的T抗原表达及生存。
Cancers (Basel). 2020 Apr 9;12(4):919. doi: 10.3390/cancers12040919.
7
Lerisetron Analogues with Antimalarial Properties: Synthesis, Structure-Activity Relationship Studies, and Biological Assessment.具有抗疟特性的来立司琼类似物:合成、构效关系研究及生物学评估。
ACS Omega. 2020 Mar 17;5(12):6967-6982. doi: 10.1021/acsomega.0c00327. eCollection 2020 Mar 31.
8
Aminoacyl tRNA synthetases as malarial drug targets: a comparative bioinformatics study.氨酰-tRNA 合成酶作为疟原虫药物靶点:比较生物信息学研究。
Malar J. 2019 Feb 6;18(1):34. doi: 10.1186/s12936-019-2665-6.
9
Potent Antimalarial 2-Pyrazolyl Quinolone (Q) Inhibitors with Improved Drug-like Properties.具有改善类药性质的强效抗疟2-吡唑基喹诺酮(Q)抑制剂
ACS Med Chem Lett. 2018 Oct 19;9(12):1205-1210. doi: 10.1021/acsmedchemlett.8b00371. eCollection 2018 Dec 13.
10
Tetrahydro-2-naphthyl and 2-Indanyl Triazolopyrimidines Targeting Plasmodium falciparum Dihydroorotate Dehydrogenase Display Potent and Selective Antimalarial Activity.靶向恶性疟原虫二氢乳清酸脱氢酶的四氢-2-萘基和2-茚基三唑并嘧啶显示出强效和选择性抗疟活性。
J Med Chem. 2016 Jun 9;59(11):5416-31. doi: 10.1021/acs.jmedchem.6b00275. Epub 2016 May 21.