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Molecular generative model based on conditional variational autoencoder for de novo molecular design
Open accessAbstract
We propose a molecular generative model based on the conditional variational autoencoder for de novo molecular design. It is specialized to control multiple molecular properties simultaneously by imposing them on a latent space. As a proof of concept, we demonstrate that it can be used to generate drug-like molecules with five target properties. We were also able to adjust a single property without changing the others and to manipulate it beyond the range of the dataset.
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“While the conditional VAE has been previously documented in the literature34, its applicability in drug design is constrained by inherent drawbacks such as sub-optimal performance on standard SMILES representations, the posterior collapse problem, and inefficient exploration of latent space.”
From PCF-VAE: posterior collapse free variational autoencoder for de novo drug design (2025) · cites this paper as [34]
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Additional file 1 of Transformer-based molecular optimization beyond matched molecular pairs
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Oestreich, M., Ewert, I., & Becker, M. (2024) · Figshare · doi:10.6084/m9.figshare.26689091
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Oestreich, M., Ewert, I., & Becker, M. (2024) · Figshare · doi:10.6084/m9.figshare.26689100
Additional file 1 of Reconstruction of lossless molecular representations from fingerprints
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Ali, A. M., Qazi, S., Almuqdadi, H. T. A., Neeraj, Majeed, O. S., Majeed, A. A., Temur, A. A., Murshedi, G. H. M. A., & Waheed, M. S. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-44415-9.00018-1
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TETGen: A Transcriptome-Guided Transformer for Targeted Molecule GenerationPreprint
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Metadata
- Authors
- Lim, J., Ryu, S., Kim, J. W., & Kim, W. Y.
- Affiliations
- Korea Advanced Institute of Science and Technology (KR)
- Corresponding author
- Kim, Jin Woo
- Kim, Woo Youn
- Venue
- Journal of Cheminformatics
- Published
- 2018-07-11
- Volume
- 10
- Issue
- 1
- Pages
- 31-31
- ISSN
- 1758-2946 (ISSN-L)
- PMC
- PMC6041224
- OpenAlex
- W2808177712
- Cited by
- 421
- References
- 23
- Citations by year
- 2026: 45 · 2025: 62 · 2024: 67 · 2023: 60 · 2022: 55 · 2021: 62 · 2020: 41 · 2019: 26 · 2018: 1
- FWCI
- 24.31
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Journal of Cheminformatics (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- arXiv (Cornell University) (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- arXiv (Cornell University)
- Figshare (cc-by)
- Funders
- National Research Foundation of Korea (NRF-2017R1E1A1A01078109)
- Topics
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Drug Discovery › Computational Drug Discovery Methods
- Physical Sciences › Materials Science › Materials Chemistry › Machine Learning in Materials Science
- Physical Sciences › Computer Science › Computer Vision and Pattern Recognition › Generative Adversarial Networks and Image Synthesis
- Keywords
- conditional variational autoencoder, de novo molecular design, generative models, latent space control, drug-like molecules, generative adversarial networks
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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