Emerging antifungal compounds and strategies targeting Candida species: a mini-review of advances from 2010 to 2025.

IF 3.3 4区 医学 Q3 CHEMISTRY, MEDICINAL
Marta Kłos, Monika Janeczko, Bartosz Mickiewicz, Paweł Kozyra, Konrad Kubiński
{"title":"Emerging antifungal compounds and strategies targeting <i>Candida</i> species: a mini-review of advances from 2010 to 2025.","authors":"Marta Kłos, Monika Janeczko, Bartosz Mickiewicz, Paweł Kozyra, Konrad Kubiński","doi":"10.1080/17568919.2026.2736311","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>The global rise of invasive and drug-resistant <i>Candida</i> infections has intensified the need for antifungal agents with novel mechanisms of action. Conventional classes of systemic drugs face limitations due to toxicity, pharmacokinetic constraints, and increasing fungi resistance, particularly among <i>C. glabrata</i> and <i>C. auris</i>. The aim of this review is to summarize the main drug candidates since 2010 in preclinical and clinical pipelines that target <i>Candida</i> spp. infections.</p><p><strong>Areas covered: </strong>This mini-review summarizes peer-reviewed studies from 2010 to 2025 investigating antifungal compounds and strategies targeting <i>Candida</i> spp. Data were compiled from several databases e.g. PubMed, PubChem, focusing on agents in laboratory, preclinical, and clinical phases that are not yet in routine use.</p><p><strong>Commentary: </strong>Promising antifungal agents are presented, including ibrexafungerp, fosmanogepix, and metallacarboranes. Some compounds demonstrate potent activity against multidrug-resistant <i>Candida</i> isolates and biofilms, with promising pharmacokinetic profiles and reduced toxicity in early studies. Post-2010 research has produced a robust antifungal pipeline with first-in-class and reformulated agents targeting <i>Candida</i> spp. Despite encouraging laboratory and early clinical findings, the efficacy and safety of these compounds must be confirmed in large randomized clinical trials before they can be incorporated into routine clinical practice.</p>","PeriodicalId":12475,"journal":{"name":"Future medicinal chemistry","volume":" ","pages":"1-12"},"PeriodicalIF":3.3000,"publicationDate":"2026-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Future medicinal chemistry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/17568919.2026.2736311","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: The global rise of invasive and drug-resistant Candida infections has intensified the need for antifungal agents with novel mechanisms of action. Conventional classes of systemic drugs face limitations due to toxicity, pharmacokinetic constraints, and increasing fungi resistance, particularly among C. glabrata and C. auris. The aim of this review is to summarize the main drug candidates since 2010 in preclinical and clinical pipelines that target Candida spp. infections.

Areas covered: This mini-review summarizes peer-reviewed studies from 2010 to 2025 investigating antifungal compounds and strategies targeting Candida spp. Data were compiled from several databases e.g. PubMed, PubChem, focusing on agents in laboratory, preclinical, and clinical phases that are not yet in routine use.

Commentary: Promising antifungal agents are presented, including ibrexafungerp, fosmanogepix, and metallacarboranes. Some compounds demonstrate potent activity against multidrug-resistant Candida isolates and biofilms, with promising pharmacokinetic profiles and reduced toxicity in early studies. Post-2010 research has produced a robust antifungal pipeline with first-in-class and reformulated agents targeting Candida spp. Despite encouraging laboratory and early clinical findings, the efficacy and safety of these compounds must be confirmed in large randomized clinical trials before they can be incorporated into routine clinical practice.

新出现的抗真菌化合物和针对念珠菌的策略:从2010年到2025年的进展综述。
导读:侵袭性和耐药念珠菌感染的全球上升加剧了对具有新型作用机制的抗真菌药物的需求。由于毒性、药代动力学的限制和真菌耐药性的增加,特别是在C. glabrata和C. auris中,常规类全身药物面临局限性。本综述的目的是总结自2010年以来针对念珠菌感染的临床前和临床管道中的主要候选药物。涵盖领域:本迷你综述总结了2010年至2025年针对念珠菌的抗真菌化合物和策略的同行评议研究。数据汇编自PubMed、PubChem等多个数据库,重点关注尚未常规使用的实验室、临床前和临床阶段的药物。评论:提出了有前途的抗真菌药物,包括ibrexafungerp, fosmangepix和金属碳硼烷。在早期研究中,一些化合物显示出对多重耐药念珠菌分离株和生物膜的有效活性,具有良好的药代动力学特征和降低毒性。2010年后的研究已经产生了一个强大的抗真菌管道,包括针对念珠菌的一流和重新配制的药物。尽管实验室和早期临床研究结果令人鼓舞,但这些化合物的有效性和安全性必须在大型随机临床试验中得到证实,然后才能纳入常规临床实践。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Future medicinal chemistry
Future medicinal chemistry CHEMISTRY, MEDICINAL-
CiteScore
5.80
自引率
2.40%
发文量
118
审稿时长
4-8 weeks
期刊介绍: Future Medicinal Chemistry offers a forum for the rapid publication of original research and critical reviews of the latest milestones in the field. Strong emphasis is placed on ensuring that the journal stimulates awareness of issues that are anticipated to play an increasingly central role in influencing the future direction of pharmaceutical chemistry. Where relevant, contributions are also actively encouraged on areas as diverse as biotechnology, enzymology, green chemistry, genomics, immunology, materials science, neglected diseases and orphan drugs, pharmacogenomics, proteomics and toxicology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书