Hybrid quantum-classical machine learning for generative chemistry and drug design: Generated molecules

DOI10.5281/zenodo.7827952Zenodo7827952MaRDI QIDQ6726291FDOQ6726291

Dataset published at Zenodo repository.

A.i. Gircha, P.o. Fedichev, K. Avchaciov, A. K. Fedorov, A.s. Boev

Publication date: 14 April 2023

Copyright license: Creative Commons Attribution 4.0 International

Description

Deep generative chemistry models emerge as powerful tools to expedite drug discovery. How- ever, the immense size and complexity of the structural space of all possible drug-like molecules pose significant obstacles, which could be overcome with hybrid architectures combining quantum computers with deep classical networks.As the first step toward this goal, we built a compact discrete variational autoencoder (DVAE) with a Restricted Boltzmann Machine (RBM) of reduced size in its latent layer. The size of the proposed model was small enough to fit on a state-of-the-art D-Wave quantum annealer and allowed training on a subset of the ChEMBL dataset of biologically active compounds. Finally, we generated 2331 novel chemical structures with medicinal chemistry and synthetic accessibility properties in the ranges typical for molecules from ChEMBL.The pre- sented results demonstrate the feasibility of using already existing or soon-to-be-available quantum computing devices as testbeds for future drug discovery applications.

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