PriMera Scientific Medicine and Public Health (ISSN: 2833-5627)

Research Article

Volume 9 Issue 1

Emerging Biological Targets: Kinases, Proteases, Ion Channels & Parasite-Specific Metabolic Pathways

Shoheb Shaikh*, Vishal Pande and Ashish Alte

July 08, 2026

Abstract

The continuous emergence of drug resistance, limitations of conventional therapeutics, and the growing burden of infectious and chronic diseases have intensified the search for novel biological targets in medicinal chemistry. Emerging biological targets such as kinases, proteases, ion channels, and parasite-specific metabolic pathways have gained substantial attention due to their pivotal roles in cellular signaling, pathogen survival, and disease progression. Protein kinases regulate numerous intracellular pathways associated with cancer, inflammatory disorders, and neurodegenerative diseases, making them attractive targets for selective therapeutic intervention. Proteases are involved in viral replication, tumor metastasis, apoptosis, and microbial virulence, thereby offering opportunities for the development of protease inhibitors with broad clinical applications. Ion channels represent crucial membrane proteins that regulate electrical signaling, neurotransmission, and ion homeostasis, and their dysregulation has been implicated in cardiovascular, neurological, and metabolic disorders. In parasitic diseases, pathogen-specific metabolic pathways provide selective drug targets with minimal host toxicity, especially in malaria, leishmaniasis, and trypanosomiasis. This mini-review highlights recent advances in the identification and therapeutic exploitation of these emerging targets, discusses current challenges associated with selectivity and resistance, and summarizes modern strategies including structure-based drug design, computational modeling, and nanotechnology-assisted delivery systems. The review underscores the importance of integrating molecular biology, medicinal chemistry, and artificial intelligence-driven approaches to accelerate the discovery of safer and more effective therapeutics.

Keywords: Kinases; Proteases; Ion Channels; Parasite-Specific Pathways; Drug Discovery; Medicinal Chemistry; Targeted Therapeutics

References

  1. Chou KC. “Impacts of bioinformatics to medicinal chemistry”. Medicinal chemistry 11.3 (2015): 218-34.
  2. Kumar A., et al. “Recent Advances in the Treatment of Parasitic Diseases: Current Status and Future”. Natural Product Based Drug Discovery Against Human Parasites: Opportunities and Challenges (2023): 249-86.
  3. Pang K., et al. “Role of protein phosphorylation in cell signaling, disease, and the intervention therapy”. MedComm 3.4 (2022): e175.
  4. Abdel-Meguid SS. “Proteases as targets for therapy”. Springer Science & Business Media (2000).
  5. Idris OA, Wintola OA and Afolayan AJ. “Helminthiases; prevalence, transmission, host-parasite interactions, resistance to common synthetic drugs and treatment”. Heliyon 5.1 (2019).
  6. Divecha VD. “Tyrosine Kinases and Its Receptors: Emphasis on Activation Signaling Pathways and Inhibitors”. African Journal of Biomedical Research (2025).
  7. Rudolph J, Hoeflich KP and Dar AC. “Contemporary design of small-molecule kinase modulators: orthosteric, allosteric and induced-proximity strategies”. Nature Reviews Drug Discovery (2026): 1-24.
  8. Elgawish MS., et al. “Leveraging artificial intelligence and machine learning in kinase inhibitor development: advances, challenges, and future prospects”. RSC Medicinal Chemistry 16.10 (2025): 4698-720.
  9. Apoorva OS., et al. “Proteases: Role in various human diseases”. Current pharmaceutical biotechnology 26.14 (2025): 2257-69.
  10. Petushkova AI and Zamyatnin Jr AA. “Papain-like proteases as coronaviral drug targets: Current inhibitors, opportunities, and limitations”. Pharmaceuticals 13.10 (2020): 277.
  11. Kuskov AN and Kukovyakina EV. “Nanotechnology-based drug delivery systems”. Pharmaceutics 17.1 (2025): 110.
  12. Khonza MM., et al. “Role of Ligand-and Voltage-Gated Ion Channels in Cell Signaling”. InCell Signaling (2025): 154-186.
  13. Zhang M., et al. “TRP (transient receptor potential) ion channel family: structures, biological functions and therapeutic interventions for diseases”. Signal Transduction and Targeted Therapy 8.1 (2023): 261.
  14. Zheng PP, Li J and Kros JM. “Breakthroughs in modern cancer therapy and elusive cardiotoxicity: Critical research‐practice gaps, challenges, and insights”. Medicinal research reviews 38.1 (2018): 325-76.
  15. Kumar A., et al. “Recent Advances in the Treatment of Parasitic Diseases: Current Status and Future”. Natural Product Based Drug Discovery Against Human Parasites: Opportunities and Challenges (2023): 249-86.
  16. Belete TM. “Recent progress in the development of new antimalarial drugs with novel targets”. Drug design, development and therapy (2020): 3875-89.
  17. Shang X., et al. “Natural products in antiparasitic drug discovery: Advances, opportunities and challenges”. Natural Product Reports 42.9 (2025): 1419-58.
  18. Siddiqui B., et al. “Artificial intelligence in computer-aided drug design (cadd) tools for the finding of potent biologically active small molecules: Traditional to modern approach”. Combinatorial Chemistry & High Throughput Screening (2025).
  19. Lytan I., et al. “Computational Innovations in Cancer Research and How Computing is Transforming Drug Discovery and Development: A Review”. Mini-Reviews in Medicinal Chemistry (2026).
  20. Suri SS, Fenniri H and Singh B. “Nanotechnology-based drug delivery systems”. Journal of occupational medicine and toxicology 2.1 (2007): 16.
  21. Doerig C. “Protein kinases as targets for anti-parasitic chemotherapy”. Biochemistry and Biophysics Acta (BBA)-Proteins and Proteomics 1697.1-2 (2004): 155-68.
  22. Abdelsayed M. “AI-driven polypharmacology in small-molecule drug discovery”. International journal of molecular sciences 26.14 (2025): 6996.
  23. Marques L., et al. “Advancing precision medicine: a review of innovative in silico approaches for drug development, clinical pharmacology and personalized healthcare”. Pharmaceutics 16.3 (2024): 332.