Evidence map›Paper›PMID 41125231›Full record

ArticleJournal of chemical information and modeling2025

Improving ADME Prediction with Multitask Graph Neural Networks and Assessing Explainability in Lead Optimization.

Shoma Ito, Takuto Koyama, Shigeyuki Matsumoto, Ryosuke Kojima, Yuji Okamoto, Masataka Kuroda, Hitoshi Kawashima, Reiko Watanabe, Tomoki Yonezawa, Takaaki Sumiyoshi and 4 more

Abstract read
In one paragraph

Article in Journal of chemical information and modeling, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Shoma ItoGraduate School of Medicine, Kyoto University, Sakyo-ku, Kyoto 606-8507, Japan.ORCID 0009-0009-1680-367X
Takuto KoyamaGraduate School of Medicine, Kyoto University, Sakyo-ku, Kyoto 606-8507, Japan.ORCID 0000-0002-9569-8370
Shigeyuki MatsumotoGraduate School of Medicine, Kyoto University, Sakyo-ku, Kyoto 606-8507, Japan.
Ryosuke KojimaGraduate School of Medicine, Kyoto University, Sakyo-ku, Kyoto 606-8507, Japan.ORCID 0000-0003-1095-8864
Yuji OkamotoGraduate School of Medicine, Kyoto University, Sakyo-ku, Kyoto 606-8507, Japan.
Masataka KurodaArtificial Intelligence Center for Health and Biomedical Research, National Institutes of Biomedical Innovation, Health and Nutrition, Settsu, Osaka 556-0022, Japan.ORCID 0000-0003-3260-9630
Hitoshi KawashimaArtificial Intelligence Center for Health and Biomedical Research, National Institutes of Biomedical Innovation, Health and Nutrition, Settsu, Osaka 556-0022, Japan.ORCID 0000-0003-3612-4294
Reiko WatanabeArtificial Intelligence Center for Health and Biomedical Research, National Institutes of Biomedical Innovation, Health and Nutrition, Settsu, Osaka 556-0022, Japan.ORCID 0000-0001-9359-8731
Tomoki YonezawaFaculty of Pharmacy, Keio University, Minato-ku, Tokyo 105-8512, Japan.
Takaaki SumiyoshiFaculty of Chemistry, Materials and Bioengineering, Kansai University, Suita, Osaka 564-8680, Japan.ORCID 0000-0002-2073-4365
Kazuyoshi IkedaFaculty of Pharmacy, Keio University, Minato-ku, Tokyo 105-8512, Japan.
Kenji MizuguchiArtificial Intelligence Center for Health and Biomedical Research, National Institutes of Biomedical Innovation, Health and Nutrition, Settsu, Osaka 556-0022, Japan.ORCID 0000-0003-3021-7078
Hiroaki IwataFaculty of Medicine, Tottori University, Yonago, Tottori 683-8503, Japan.ORCID 0000-0001-9791-0008
Yasushi OkunoGraduate School of Medicine, Kyoto University, Sakyo-ku, Kyoto 606-8507, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early evaluation of absorption, distribution, metabolism, and excretion (ADME) properties is crucial for streamlining drug development. Traditional in vivo and in vitro approaches are often expensive. Moreover, during lead optimization, these methods rely heavily on the expertise of specialists, leading to efficiency challenges. Consequently, in silico methods for ADME prediction are attracting increasing attention. However, existing in silico methods face two major issues: a decline in predictive performance caused by limited ADME data and a lack of clarity regarding the rationale for lead optimization to improve ADME properties. In this study, we built an AI model capable of predicting ten different ADME parameters to overcome these challenges. Our training approach was based on a graph neural network combining multitask learning, which shares information across multiple tasks to increase the number of usable samples, with fine-tuning that adapts to each task. In addition, we applied the integrated gradients method to compound data collected before and after lead optimization to quantify and interpret each input feature's contribution to the predicted ADME values. Our proposed model achieved the highest performance for seven of the ten ADME parameters compared with conventional methods. Furthermore, visualization of the changes in chemical structures before and after lead optimization revealed that the model's explanations aligned well with established chemical insights. These results suggest that data-driven approaches may assist molecular design by providing complementary insights into empirical rules.

Indexed as

Neural Networks, ComputerGraph Neural NetworksHumansPharmaceutical PreparationsPharmaceutical Preparations

Identifiers

PMID41125231
PMCPMC12606635

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Registered trials

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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.