mlsanityData to 7 Oct 2026

Repurformer: Transformers for Repurposing-Aware Molecule Generation

arXiv 2407.11439 ↗First posted 16 Jul 2024cs.LG cs.AI q-bio.BMcited by 1

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Abstract (arXiv)

Generating as diverse molecules as possible with desired properties is crucial for drug discovery research, which invokes many approaches based on deep generative models today. Despite recent advancements in these models, particularly in variational autoencoders (VAEs), generative adversarial networks (GANs), Transformers, and diffusion models, a significant challenge known as textitthe sample bias problem remains. This problem occurs when generated molecules targeting the same protein tend to be structurally similar, reducing the diversity of generation. To address this, we propose leveraging multi-hop relationships among proteins and compounds. Our model, Repurformer, integrates bi-directional pretraining with Fast Fourier Transform (FFT) and low-pass filtering (LPF) to capture complex interactions and generate diverse molecules. A series of experiments on BindingDB dataset confirm that Repurformer successfully creates substitutes for anchor compounds that resemble positive compounds, increasing diversity between the anchor and generated compounds.

Key facts. Cited by 1 paper in the map (data through 7 Oct 2026). Builds on 13 of its 42 references that are in the map. First posted on arXiv 16 Jul 2024.

Builds on

13 of 42 references.

References · 13

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1 more
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Citing papers per year: 2025: 1.

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  2. 2025From In Silico to In Vitro: Evaluating Molecule Generative Models for Hit Generation
  3. 2025NEAT: Neighborhood-Guided, Efficient, Autoregressive Set Transformer for 3D Molecular Generation
  4. 2026SynLaD: Latent Diffusion for Generating Synthesizable Molecules Conditioned on 3D Pharmacophore Profiles
  5. 2024Rectified Flow For Structure Based Drug Design
  6. 2022DiffBP: Generative Diffusion of 3D Molecules for Target Protein Binding
  7. 2024Physics-informed generative model for drug-like molecule conformers
  8. 2024Can LLMs Generate Diverse Molecules? Towards Alignment with Structural Diversity