Samuel Thompson*
Department of Organic & Medicinal Chemistry, University of Toronto, Canada
Received: 02-Sep-2025, Manuscript No. jomc-25-177972; Editor assigned: 4-Sep-2025, Pre-QC No. jomc-25-177972 (PQ); Reviewed: 14-Sep-2025, QC No jomc-25-177972; Revised: 20-Sep-2025, Manuscript No. jomc-25-177972 (R); Published: 28-Sep-2025, DOI: 10.4172/ jomc.12.011
Citation: Samuel Thompson, Drug Design and Discovery: From Concept to Cure. J Med Orgni Chem. 2025.12.011.
Copyright: © 2025 Samuel Thompson, this is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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Drug design and discovery is a fundamental scientific process focused on developing new therapeutic agents to prevent, manage, or cure diseases. It combines principles from chemistry, biology, pharmacology, and computational science to identify molecules capable of interacting with specific biological targets. As diseases become more complex and resistant to existing treatments, the need for innovative and efficient drug discovery strategies has increased. Modern drug design emphasizes precision, safety, and effectiveness, moving beyond traditional methods toward rational and targeted approaches [1, 2].
The process of drug discovery begins with target identification and validation. A target is usually a protein, enzyme, or receptor involved in disease progression. Once identified, scientists confirm that modifying the target can produce a therapeutic benefit. Following this, potential drug candidates are identified through methods such as high-throughput screening, where thousands of compounds are tested, or structure-based drug design, which uses the three-dimensional structure of the target to design effective molecules [3].
After initial screening, promising compounds known as lead molecules undergo optimization. This stage focuses on improving potency, selectivity, bioavailability, and safety. Medicinal chemists modify chemical structures to enhance binding to the target while minimizing side effects. Simultaneously, pharmacokinetic and pharmacodynamic studies evaluate how the drug behaves in the body, including absorption, distribution, metabolism, and excretion [5].
Preclinical testing is then conducted using laboratory and animal models to assess safety and efficacy. Successful candidates proceed to clinical trials, which are carried out in multiple phases to evaluate safety, dosage, and therapeutic effectiveness in humans. Despite significant advancements, drug discovery remains a time-consuming and costly process, with a high rate of failure. To address these challenges, emerging technologies such as artificial intelligence, machine learning, and bioinformatics are increasingly being used to predict outcomes, identify novel targets, and reduce development timelines.
Drug design and discovery plays a vital role in advancing modern medicine and improving patient outcomes. Although the process is complex and resource-intensive, continuous scientific and technological innovations have enhanced efficiency and success rates. The integration of computational tools, molecular biology, and interdisciplinary collaboration has transformed traditional drug development into a more rational and targeted endeavor. As research continues to evolve, drug discovery is expected to become faster, more accurate, and increasingly personalized, offering new hope for the treatment of both existing and emerging diseases.