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本文引用的文献

1
Repositionable Compounds with Antifungal Activity against Multidrug Resistant Identified in the Medicines for Malaria Venture's Pathogen Box.在疟疾药物风险投资公司的病原体库中鉴定出的对多重耐药菌具有抗真菌活性的可重新定位化合物。
J Fungi (Basel). 2019 Oct 1;5(4):92. doi: 10.3390/jof5040092.
2
The fungal mycobiome promotes pancreatic oncogenesis via activation of MBL.真菌微生物组通过激活 MBL 促进胰腺发生癌变。
Nature. 2019 Oct;574(7777):264-267. doi: 10.1038/s41586-019-1608-2. Epub 2019 Oct 2.
3
Adjunctive sertraline for HIV-associated cryptococcal meningitis: a randomised, placebo-controlled, double-blind phase 3 trial.辅助舍曲林治疗 HIV 相关隐球菌性脑膜炎:一项随机、安慰剂对照、双盲 3 期试验。
Lancet Infect Dis. 2019 Aug;19(8):843-851. doi: 10.1016/S1473-3099(19)30127-6.
4
Host Carbon Dioxide Concentration Is an Independent Stress for Cryptococcus neoformans That Affects Virulence and Antifungal Susceptibility.宿主二氧化碳浓度是新型隐球菌的独立应激源,影响其毒力和抗真菌药物敏感性。
mBio. 2019 Jul 2;10(4):e01410-19. doi: 10.1128/mBio.01410-19.
5
Zinc and Iron Homeostasis: Target-Based Drug Screening as New Route for Antifungal Drug Development.锌铁稳态:基于靶点的药物筛选——抗真菌药物研发的新途径
Front Cell Infect Microbiol. 2019 May 29;9:181. doi: 10.3389/fcimb.2019.00181. eCollection 2019.
6
Identification of Off-Patent Compounds That Present Antifungal Activity Against the Emerging Fungal Pathogen .鉴定具有抗新兴真菌病原体的抗真菌活性的非专利化合物。
Front Cell Infect Microbiol. 2019 Apr 2;9:83. doi: 10.3389/fcimb.2019.00083. eCollection 2019.
7
The Zebrafish as a Model Host for Invasive Fungal Infections.斑马鱼作为侵袭性真菌感染的模型宿主
J Fungi (Basel). 2018 Dec 13;4(4):136. doi: 10.3390/jof4040136.
8
Alexidine Dihydrochloride Has Broad-Spectrum Activities against Diverse Fungal Pathogens.盐酸阿比多尔对多种真菌病原体具有广泛的活性。
mSphere. 2018 Oct 31;3(5):e00539-18. doi: 10.1128/mSphere.00539-18.
9
Screening a Repurposing Library for Inhibitors of Multidrug-Resistant Candida auris Identifies Ebselen as a Repositionable Candidate for Antifungal Drug Development.筛选再利用库以寻找抗多药耐药性耳念珠菌的抑制剂,发现乙硒啉可作为重新定位的抗真菌药物开发候选物。
Antimicrob Agents Chemother. 2018 Sep 24;62(10). doi: 10.1128/AAC.01084-18. Print 2018 Oct.
10
Activity of novel antifungal compound APX001A against a large collection of Candida auris.新型抗真菌化合物 APX001A 对大量耳念珠菌的活性。
J Antimicrob Chemother. 2018 Nov 1;73(11):3060-3062. doi: 10.1093/jac/dky302.

抗真菌药物筛选:跳出固有思维,寻找新型抗真菌支架。

Antifungal drug screening: thinking outside the box to identify novel antifungal scaffolds.

机构信息

Department of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, IA, United States.

Department of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, IA, United States; Department of Microbiology and Immunology, Carver College of Medicine, University of Iowa, Iowa City, IA, United States.

出版信息

Curr Opin Microbiol. 2020 Oct;57:1-6. doi: 10.1016/j.mib.2020.03.005. Epub 2020 Apr 24.

DOI:10.1016/j.mib.2020.03.005
PMID:32339892
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7652037/
Abstract

Invasive fungal infections are responsible for a significant disease burden worldwide. Drugs to treat these infections are limited to only four unique classes, and despite these available treatments, mortality rates remain unacceptably high. In this review, we will discuss antifungal drug screening and how the approach to identifying novel compounds needs move away from traditional growth-based assays in order to meet the demand for new drugs. We highlight specific examples of creative screening strategies that increase the likelihood of identifying compounds with desired activities and provide perspective to inspire development of novel screens for the identification of first-in-class antifungals.

摘要

侵袭性真菌感染在全球范围内造成了巨大的疾病负担。用于治疗这些感染的药物仅局限于四种独特的类别,尽管有这些可用的治疗方法,但死亡率仍然高得不可接受。在这篇综述中,我们将讨论抗真菌药物的筛选,以及为了满足新药的需求,确定新型化合物的方法需要如何摆脱传统的基于生长的检测方法。我们重点介绍了一些有创意的筛选策略的具体例子,这些策略增加了发现具有所需活性的化合物的可能性,并提供了新的视角来启发用于鉴定新型抗真菌药物的新筛选方法的开发。