Evidence map›Paper›PMID 39921889›Full record

ArticleBioinformatics (Oxford, England)2025

MolFCL: predicting molecular properties through chemistry-guided contrastive and prompt learning.

Xiang Tang, Qichang Zhao, Jianxin Wang, Guihua Duan

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Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xiang TangHunan Provincial Key Lab on Bioinformatics, School of Computer Science and Engineering, Central South University, Changsha 410083, China.
Qichang ZhaoHunan Provincial Key Lab on Bioinformatics, School of Computer Science and Engineering, Central South University, Changsha 410083, China.ORCID 0000-0002-8319-9793
Jianxin WangHunan Provincial Key Lab on Bioinformatics, School of Computer Science and Engineering, Central South University, Changsha 410083, China.ORCID 0000-0003-1516-0480
Guihua DuanHunan Provincial Key Lab on Bioinformatics, School of Computer Science and Engineering, Central South University, Changsha 410083, China.

Funding

National Natural Science Foundation of China 62350004Project of Xiangjiang Laboratory 23XJ01011
6 · The paper itself

Abstract

motivationAccurately identifying and predicting molecular properties is a crucial task in molecular machine learning, and the key lies in how to extract effective molecular representations. Contrastive learning opens new avenues for representation learning, and a large amount of unlabeled data enables the model to generalize to the huge chemical space. However, existing contrastive learning-based models face two challenges: (i) existing methods destroy the original molecular environment and ignore chemical prior information, and (ii) there is a lack of a prior knowledge to guide the prediction of molecular properties.

resultsIn this work, we propose a molecular property prediction framework called MolFCL, which consists of fragment-based contrastive learning and functional group-based prompt learning. Specifically, we introduced fragment-fragment interactions for the first time in the contrastive learning framework and designed a fragment-based augmented molecular graph that integrates the original chemical environment and fragment reactions. Furthermore, we proposed a novel functional group-based prompt learning during fine-tuning, which first incorporates functional group knowledge and the corresponding atomic signals, to improve molecular representation and provide interpretable analyses. The results show that MolFCL outperforms state-of-the-art baseline models on 23 molecular property prediction datasets. Moreover, visualizations show that MolFCL can learn to embed molecules into representations that can distinguish chemical properties. MolFCL can give higher weight to functional groups consistent with chemical knowledge during the prediction of molecular properties, which offers an interpretable ability of the model. Overall, MolFCL is a practically useful tool for molecular property prediction and assists drug scientists in designing drugs more effectively. AVAILABILITY AND IMPLEMENTATION: MolFCL is available at https://github.com/tangxiangcsu/MolFCLSupplementary.

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Computational BiologyMachine LearningSoftwareAlgorithms

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PMID39921889
PMCPMC11878793

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.