druGAN: An Advanced Generative Adversarial Autoencoder Model for de Novo Generation of New Molecules with Desired Molecular Properties in Silico

被引:410
作者
Kadurin, Artur [1 ,3 ,7 ]
Nikolenko, Sergey [2 ,3 ,7 ]
Khrabrov, Kuzma [4 ]
Aliper, Alex [1 ]
Zhavoronkov, Alex [1 ,5 ,6 ]
机构
[1] Johns Hopkins Univ Eastern, Emerging Technol Ctr, Insilico Med Inc, Pharmaceut Artificial Intelligence Dept, Baltimore, MD 21218 USA
[2] Natl Res Univ, Higher Sch Econ, St Petersburg 190008, Russia
[3] Steklov Math Inst St Petersburg, St Petersburg 191023, Russia
[4] Mail Ru Grp Ltd, Search Dept, Moscow 125167, Russia
[5] Biogerontol Res Fdn, Trevissome Pk, Truro TR4 8UN, England
[6] Moscow Inst Phys & Technol, Dolgoprudnyi 141701, Russia
[7] Kazan Fed Univ, Kazan 420008, Republic Of Tat, Russia
关键词
adversarial autoencoder; deep learning; drug discovery; variational autoencoder; generative adversarial network; NEURAL-NETWORKS;
D O I
10.1021/acs.molpharmaceut.7b00346
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Deep generative adversarial networks (GANs) are the emerging technology in drug discovery and biomarker development. In our recent work, we demonstrated a proof-of-concept of implementing deep generative adversarial autoencoder (AAE) to identify new molecular fingerprints with predefined anticancer properties. Another popular generative model is the variational autoencoder (VAE), which is based on deep neural architectures. In this work, we developed an advanced AAE model for molecular feature extraction problems, and demonstrated its advantages compared to VAE in terms of (a) adjustability in generating molecular fingerprints; (b) capacity of processing very large molecular data sets; and (c) efficiency in unsupervised pretraining for regression model. Our results suggest that the proposed AAE model significantly enhances the capacity and efficiency of development of the new molecules with specific anticancer properties using the deep generative models.
引用
收藏
页码:3098 / 3104
页数:7
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