Estimation of Synthetic Accessibility during Computational Drug Design

被引:0
|
作者
Vorsilak, Milan [1 ,2 ]
Svozil, Daniel [1 ,2 ]
机构
[1] AV CR Vvi, Ustav Mol Genet, CZ OPENSCREEN Narodni Infrastruktura Chem Biol, Videnska 1083, Prague 14220 4, Czech Republic
[2] Vysoka Skola Chem Technol Praze, Fak Chem Technol, Lab Informat & Chem, CZ OPENSCREEN Narodni Infrastruktura Chem Biol,Te, Prague 16628 6, Czech Republic
来源
CHEMICKE LISTY | 2017年 / 111卷 / 11期
关键词
chemical space; synthetic feasibility; retrosynthetic analysis; molecular complexity; virtual screening; computational drug design; AIDED SYNTHESIS DESIGN; ARTIFICIAL-INTELLIGENCE; MOLECULAR COMPLEXITY; CHEMICAL-SYNTHESIS; MACHINE; GENERATION; PREDICTION; DISCOVERY; UNIVERSE; SYSTEMS;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Virtual screening makes it possible to design and then test up to millions of structures. On the other hand, not every virtual structure can readily be prepared and tested in reality. Therefore, it is necessary to exclude unsuitable candidates, ideally at the beginning of virtual screening campaign. Three main approaches are used to filter out synthetically unfeasible structures: similarity to starting material, retrosynthetic route and complexity of the structure. These techniques vary in computational demands; they can therefore be used in various stages of screening, and/or combined to improve estimation of synthetic feasibility.
引用
收藏
页码:760 / 765
页数:6
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