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Small molecule approaches to targeting RNA
被引:19
|作者:
Kovachka, Sandra
[1
]
Panosetti, Marc
[1
,2
]
Grimaldi, Benedetto
[2
]
Azoulay, Stephane
[1
]
Di Giorgio, Audrey
[1
]
Duca, Maria
[1
]
机构:
[1] Univ Cote dAzur, Inst Chem Nice, CNRS, Nice, France
[2] Ist Italiano Tecnol IIT, Mol Med Res Line, Genoa, Italy
关键词:
SEQUENCE-BASED DESIGN;
ONCOGENIC MICRORNAS;
DYSTROPHY TYPE-1;
RATIONAL DESIGN;
AMINOGLYCOSIDE;
DISCOVERY;
BINDING;
DRUG;
PERSPECTIVES;
CLEAVAGE;
D O I:
10.1038/s41570-023-00569-9
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The development of innovative methodologies to identify RNA binders has attracted enormous attention in chemical biology and drug discovery. Although antibiotics targeting bacterial ribosomal RNA have been on the market for decades, the renewed interest in RNA targeting reflects the need to better understand complex intracellular processes involving RNA. In this context, small molecules are privileged tools used to explore the biological functions of RNA and to validate RNAs as therapeutic targets, and they eventually are to become new drugs. Despite recent progress, the rational design of specific RNA binders requires a better understanding of the interactions which occur with the RNA target to reach the desired biological response. In this Review, we discuss the challenges to approaching this underexplored chemical space, together with recent strategies to bind, interact and affect biologically relevant RNAs. This Review highlights the strategies and challenges for targeting RNA with small molecules in medicinal chemistry. It emphasizes their potential as drugs and tools for understanding complex biological processes while encouraging chemists to contribute to this field for future advances.
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页码:120 / 135
页数:16
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