ICVAE: Interpretable Conditional Variational Autoencoder for De Novo Molecular Design

Recent studies have demonstrated that machine learning-based generative models can create novel molecules with desirable properties. Among them, Conditional Variational Autoencoder (CVAE) is a powerful approach to generate molecules with desired physiochemical and pharmacological properties. However, the CVAE's latent space is still a black-box, making it difficult to understand the relationship between the latent space and molecular properties. To address this issue, we propose the Interpretable Conditional Variational Autoencoder (ICVAE), which introduces a modified loss function that correlates the latent value with molecular properties. ICVAE established a linear mapping between latent variables and molecular properties. This linearity is not only crucial for improving interpretability, by assigning clear semantic meaning to latent dimensions, but also provides a practical advantage. It enables direct manipulation of molecular attributes through simple coordinate shifts in latent space, rather than relying on opaque, black-box optimization algorithms. Our experimental results show that the ICVAE can linearly relate one or multiple molecular properties with the latent value and generate molecules with precise properties by controlling the latent values. The ICVAE's interpretability allows us to gain insight into the molecular generation process, making it a promising approach in drug discovery and material design.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-04-23
DOI
https://doi.org/10.3390/ijms26093980
Citations
6
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
9.03

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article

ICVAE: Interpretable Conditional Variational Autoencoder for De Novo Molecular Design

Xiaozhen Ren, Senlin Fang, Hongchao Ji, Molin Yue et al.
6 citations
International Journal of Molecular Sciences
Computational Drug Discovery Methods
9.03
article

ICVAE: Interpretable Conditional Variational Autoencoder for De Novo Molecular Design

Xiaozhen Ren, Senlin Fang, Hongchao Ji, Molin Yue, Xiaqiong Fan, Jiamin Li, Zhengyan Li
article en
6 citations

Abstract

Recent studies have demonstrated that machine learning-based generative models can create novel molecules with desirable properties. Among them, Conditional Variational Autoencoder (CVAE) is a powerful approach to generate molecules with desired physiochemical and pharmacological properties. However, the CVAE's latent space is still a black-box, making it difficult to understand the relationship between the latent space and molecular properties. To address this issue, we propose the Interpretable Conditional Variational Autoencoder (ICVAE), which introduces a modified loss function that correlates the latent value with molecular properties. ICVAE established a linear mapping between latent variables and molecular properties. This linearity is not only crucial for improving interpretability, by assigning clear semantic meaning to latent dimensions, but also provides a practical advantage. It enables direct manipulation of molecular attributes through simple coordinate shifts in latent space, rather than relying on opaque, black-box optimization algorithms. Our experimental results show that the ICVAE can linearly relate one or multiple molecular properties with the latent value and generate molecules with precise properties by controlling the latent values. The ICVAE's interpretability allows us to gain insight into the molecular generation process, making it a promising approach in drug discovery and material design.

International Journal of Molecular SciencesVol. 26(9)
Henan University (CN), Henan University of Technology (CN), Agricultural Genomics Institute at Shenzhen (CN), Chinese Academy of Agricultural Sciences (CN)
Henan University of Technology, Henan University, Science and Technology Department of Henan Province, National Key Research and Development Program of China
Openalex Percentile: Top 2%
Computational Drug Discovery Methods
9.03
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