Leveraging artificial intelligence and machine learning in kinase inhibitor development: advances, challenges, and

Mohamed S Elgawish1,2, Aya M Almatary3, Sawsan A Zaitone4,5

  • 1Medicinal Chemistry Department, Faculty of Pharmacy, Suez Canal University Ismailia 41522 Egypt mohamed_elgawish@pharm.suez.edu.eg +20643230741 +82109893 8184.

RSC Medicinal Chemistry
|September 8, 2025
PubMed

Insights

Artificial intelligence (AI) and machine learning (ML) are revolutionizing kinase inhibitor drug discovery by addressing challenges like target identification and resistance. These computational methods accelerate the development of next-generation kinase-targeted therapeutics.

Area of Science:

  • Biochemistry and Pharmacology
  • Computational Biology and Bioinformatics
  • Drug Discovery and Development

Background:

  • Protein kinases are crucial cell signaling regulators implicated in cancer and autoimmune diseases.
  • Kinase inhibitors like imatinib demonstrate therapeutic value, but challenges persist in developing selective and potent drugs.
  • The conserved ATP-binding site, off-target effects, resistance, and patient variability complicate kinase inhibitor development.

Purpose of the Study:

  • To review the transformative applications of AI and ML in designing, optimizing, and repurposing kinase inhibitors.
  • To explore how AI/ML methods address key obstacles in kinase-targeted drug discovery.
  • To highlight the potential of AI/ML in accelerating the development of novel kinase inhibitors.

Main Methods:

  • Review of AI/ML methodologies including deep learning, graph neural networks, and generative models.
  • Analysis of AI/ML applications across the drug discovery pipeline: target identification, virtual screening, SAR modeling, resistance prediction, and clinical trial design.
  • Examination of case studies showcasing AI-optimized kinase inhibitors (e.g., BTK, EGFR).

Main Results:

  • AI/ML methods offer solutions for challenges such as target identification, virtual screening, and predicting drug resistance.
  • Case studies demonstrate the real-world impact of AI in optimizing kinase inhibitors.
  • Current limitations include data sparsity, model interpretability, and the gap between computational and experimental findings.

Conclusions:

  • AI/ML integration with medicinal chemistry promises to accelerate and refine kinase inhibitor development.
  • Emerging directions include federated learning, personalized kinase inhibitors, and AI-enabled combination therapies.
  • AI/ML holds significant potential for advancing the next generation of kinase-targeted therapeutics.

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