计算机科学
生物信息学
化学空间
过程(计算)
化学信息学
预处理器
钥匙(锁)
芯(光纤)
编码(集合论)
虚拟筛选
药物发现
化学
程序设计语言
集合(抽象数据类型)
电信
生物化学
计算机安全
基因
计算化学
作者
Vendy Fialková,Jiaxi Zhao,Kostas Papadopoulos,Ola Engkvist,Esben Jannik Bjerrum,Thierry Kogej,Atanas Patronov
标识
DOI:10.1021/acs.jcim.1c00469
摘要
Because of the strong relationship between the desired molecular activity and its structural core, the screening of focused, core-sharing chemical libraries is a key step in lead optimization. Despite the plethora of current research focused on in silico methods for molecule generation, to our knowledge, no tool capable of designing such libraries has been proposed. In this work, we present a novel tool for de novo drug design called LibINVENT. It is capable of rapidly proposing chemical libraries of compounds sharing the same core while maximizing a range of desirable properties. To further help the process of designing focused libraries, the user can list specific chemical reactions that can be used for the library creation. LibINVENT is therefore a flexible tool for generating virtual chemical libraries for lead optimization in a broad range of scenarios. Additionally, the shared core ensures that the compounds in the library are similar, possess desirable properties, and can also be synthesized under the same or similar conditions. The LibINVENT code is freely available in our public repository at https://github.com/MolecularAI/Lib-INVENT. The code necessary for data preprocessing is further available at: https://github.com/MolecularAI/Lib-INVENT-dataset.
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