化学
药效团
药物发现
化学空间
脚手架
纳米技术
计算生物学
组合化学
生物化学
立体化学
计算机科学
材料科学
数据库
生物
作者
Timothy B. Callis,Taylor R. Garrett,Andrew P. Montgomery,Jonathan J. Danon,Michael Kassiou
标识
DOI:10.1021/acs.jmedchem.2c00969
摘要
The concept of bioisosterism and the implementation of bioisosteric replacement is fundamental to medicinal chemistry. The exploration of bioisosteres is often used to probe key structural features of candidate pharmacophores and enhance pharmacokinetic properties. As the understanding of bioisosterism has evolved, capabilities to undertake more ambitious bioisosteric replacements have emerged. Scaffold hopping is a broadly used term in the literature referring to a variety of different bioisosteric replacement strategies, ranging from simple heterocyclic replacements to topological structural overhauls. In this work, we have highlighted recent applications of scaffold hopping in the central nervous system drug discovery space. While we have highlighted the benefits of using scaffold hopping approaches in central nervous system drug discovery, these are also widely applicable to other medicinal chemistry fields. We also recommend a shift toward the use of more refined and meaningful terminology within the realm of scaffold hopping.
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