化学
化学信息学
化学空间
虚拟筛选
计算机科学
生物信息学
数量结构-活动关系
药物发现
人工智能
人工神经网络
Python(编程语言)
化学数据库
公共化学
机器学习
计算生物学
化学
生物信息学
生物
程序设计语言
生物化学
基因
作者
Peter Ertl,Richard A. Lewis,Éric Martin,Valery Polyakov
出处
期刊:Cornell University - arXiv
日期:2017-01-01
被引量:34
标识
DOI:10.48550/arxiv.1712.07449
摘要
The exploration of novel chemical spaces is one of the most important tasks of cheminformatics when supporting the drug discovery process. Properly designed and trained deep neural networks can provide a viable alternative to brute-force de novo approaches or various other machine-learning techniques for generating novel drug-like molecules. In this article we present a method to generate molecules using a long short-term memory (LSTM) neural network and provide an analysis of the results, including a virtual screening test. Using the network one million drug-like molecules were generated in 2 hours. The molecules are novel, diverse (contain numerous novel chemotypes), have good physicochemical properties and have good synthetic accessibility, even though these qualities were not specific constraints. Although novel, their structural features and functional groups remain closely within the drug-like space defined by the bioactive molecules from ChEMBL. Virtual screening using the profile QSAR approach confirms that the potential of these novel molecules to show bioactivity is comparable to the ChEMBL set from which they were derived. The molecule generator written in Python used in this study is available on request.
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