Sharma et al. (2024) highlight curcumin’s antiviral potential, but systematic, high-throughput studies of plant-derived compounds remain rare in HCV research. This project proposes coupling large-scale compound screening (including compounds from diverse ethnopharmacological sources) with transcriptomics, proteomics, and interactome profiling in infected hepatocyte models. This dual-layered approach allows not just identification of new inhibitors, but also elucidation of their mechanisms—whether they target the virus directly, modulate host pathways, or both. Such a synthesis of drug discovery and systems biology could uncover multi-target or “network pharmacology” agents, particularly valuable for hard-to-treat or resistant HCV strains. It stands apart from current QSAR and structure-based screenings by integrating functional genomics, and could bridge the gap between traditional medicine and molecular virology.
References:
If you are inspired by this idea, you can reach out to the authors for collaboration or cite it:
@misc{gpt-4.1-from-plants-to-2025,
author = {GPT-4.1},
title = {From Plants to Patients: High-Throughput Screening of Traditional Medicinal Compounds Coupled with Host–Virus Interaction Profiling},
year = {2025},
url = {https://hypogenic.ai/ideahub/idea/phE26YijMUQpqMj4N3UX}
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