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Repurposing and optimization of drugs for discovery of novel antifungals
被引:19
|作者:
Donlin, Maureen J.
[1
,3
]
Meyers, Marvin J.
[2
,3
]
机构:
[1] St Louis Univ, Edward A Doisy Dept Biochem & Mol Biol, Sch Med, St Louis, MO 63104 USA
[2] St Louis Univ, Dept Chem, St Louis, MO USA
[3] St Louis Univ, Inst Drug & Biotherapeut Innovat, St Louis, MO 63103 USA
基金:
美国国家卫生研究院;
关键词:
Anti-fungal drug development;
Drug repurposing;
Lead optimization;
SOSA;
EPIDEMIOLOGY;
D O I:
10.1016/j.drudis.2022.04.021
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Although fungal diseases are a major and growing public health concern, there are only four major classes of drug to treat primary fungal pathogens. The pipeline of new antifungals in clinical development is relatively thin compared with other disease classes. One approach to rapidly identify and provide novel treatment options is to repurpose existing drugs as antifungals. However, such proposed drug-repurposing candidates often suffer suboptimal efficacy and pharmacokinetics (PK) for fungal diseases. Herein, we briefly review the current antifungal drug pipeline and recent approaches to optimize existing drugs into novel molecules with unique modes of action relative to existing antifungal drug classes.
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页码:2008 / 2014
页数:7
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