Evidence map›Paper›PMID 40461636›Full record

ArticleScientific reports2025

Predicting drug-target interactions using machine learning with improved data balancing and feature engineering.

Md Alamin Talukder, Mohsin Kazi, Ammar Alazab

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Artificial Intelligence Across the Drug Development Lifecycle.Medical sciences (Basel, Switzerland) · 2026
    Review
  3. Article
  4. Article
  5. 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

3 authors.

Md Alamin TalukderDepartment of Computer Science and Engineering, International University of Business Agriculture and Technology, Dhaka, Bangladesh. alamin.cse@iubat.edu.
Mohsin KaziDepartment of Pharmaceutics, College of Pharmacy, King Saud University, P.O. BOX-2457, Riyadh, 11451, Saudi Arabia. mkazi@ksu.edu.sa.
Ammar AlazabCyber Security and Digital Technology, Victoria University, VIC, Australia. ammar.alazab@torrens.edu.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug-Target Interaction (DTI) prediction is a vital task in drug discovery, yet it faces significant challenges such as data imbalance and the complexity of biochemical representations. This study makes several contributions to address these issues, introducing a novel hybrid framework that combines advanced machine learning (ML) and deep learning (DL) techniques. The framework leverages comprehensive feature engineering, utilizing MACCS keys to extract structural drug features and amino acid/dipeptide compositions to represent target biomolecular properties. This dual feature extraction method enables a deeper understanding of chemical and biological interactions, enhancing predictive accuracy. To address data imbalance, Generative Adversarial Networks (GANs) are employed to create synthetic data for the minority class, effectively reducing false negatives and improving the sensitivity of the predictive model. The Random Forest Classifier (RFC) is utilized to make precise DTI predictions, optimized for handling high-dimensional data. The proposed framework's scalability and robustness were validated across diverse datasets, including BindingDB-Kd, BindingDB-Ki, and BindingDB-IC50. For the BindingDB-Kd dataset, the GAN+RFC model achieved remarkable performance metrics: accuracy of 97.46%, precision of 97.49%, sensitivity of 97.46%, specificity of 98.82%, F1-score of 97.46%, and ROC-AUC of 99.42%. Similarly, for the BindingDB-Ki dataset, the model attained an accuracy of 91.69%, precision of 91.74%, sensitivity of 91.69%, specificity of 93.40%, F1-score of 91.69%, and ROC-AUC of 97.32%. On the BindingDB-IC50 dataset, the model achieved an accuracy of 95.40%, precision of 95.41%, sensitivity of 95.40%, specificity of 96.42%, F1-score of 95.39%, and ROC-AUC of 98.97%. These results demonstrate the efficacy of the GAN-based approach in capturing complex patterns, significantly improving DTI prediction outcomes. In conclusion, the proposed GAN-based hybrid framework sets a new benchmark in computational drug discovery by addressing critical challenges in DTI prediction. Its robust performance, scalability, and generalizability contribute substantially to therapeutic development and pharmaceutical research.

Indexed as

Drug DiscoveryMachine LearningDeep LearningHumansComputational drug discoveryData imbalanceDrug-Target interactionGenerative adversarial networksMachine learningRandom forest classifier

Identifiers

PMID40461636
PMCPMC12134243

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.