Benign-by-design chemistry: Reinventing ligand-based drug design at the edge of AI
Ligand-based drug design (LBDD) has long driven therapeutic innovation; however, its traditional potency-centered paradigm often oversimplifies biological complexity. Advances in artificial intelligence (AI) now enable multiobjective strategies that integrate polypharmacology, safety and environmental sustainability. Despite this progress, a unified framework that systematically incorporates these dimensions within AI-augmented LBDD is lacking. Here, we propose that embedding benign-by-design principles into multiobjective optimization can enable the proactive mitigation of toxicity, off-target effects and ecological impact from the early design and discovery stages. This shift redefines LBDD as a complexity-aware and ethically grounded discipline capable of delivering safer and more sustainable therapeutics. Accordingly, the primary objective of this review is to outline a unifying framework for AI-enabled LBDD that moves beyond potency-centered optimization by integrating efficacy, safety, sustainability and societal impact.
Authors
- Diana V. Ávila-Martínez
- José L. Medina-Franco
- Angel N. Toto-Vazquez
- Ola Spjuth
- Pamela I. Hernández-Estrada
- Edgar López-López
Institutions
- Universidad Veracruzana (MX)
- Science for Life Laboratory (SE)
- Universidad Nacional Autónoma de México (MX)
Publication Details
- Journal
- Drug Discovery Today
- Published
- 2026-05-01
- DOI
- https://doi.org/10.1016/j.drudis.2026.104691
- Primary Topic
- Computational Drug Discovery Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00