Drug repurposing: A futuristic approach in drug discovery

Saba Khan, J. Agnihotri, Sunanda R. Patil, N. Khan
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Abstract

Drug repurposing (DR), also known as drug repositioning, is a strategy aimed at identifying new therapeutic uses for existing drugs. It offers an effective approach to discovering or developing drug molecules with novel pharmacological or therapeutic indications. In recent years, pharmaceutical companies have increasingly embraced the drug repurposing strategy in their drug discovery and development programs, leading to the identification of new biological targets. This strategy is highly efficient, time-saving, cost-effective, and carries a lower risk of failure compared to traditional drug discovery methods. By maximizing the therapeutic value of existing drugs, drug repurposing increases the likelihood of success. It serves as a valuable alternative to the lengthy, expensive, and resource-intensive process of finding new molecular entities (NMEs) through traditional or de novo drug discovery approaches. Drug repurposing combines activity-based or experimental methods with in silico-based or computational approaches to rationally develop or identify new uses for drug molecules. It leverages the existing safety data of drugs tested in humans and redirects their application based on valid target molecules. This approach holds great promise, particularly in addressing rare, difficult-to-treat diseases, and neglected diseases. By utilizing the wealth of knowledge and resources available, drug repurposing presents an emerging strategy for optimizing the therapeutic potential of existing medicines. It offers a pathway to rapidly identify effective treatments and repurpose approved drugs for new indications, benefiting patients and healthcare systems alike.
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药物再利用:药物发现的未来方法
药物再利用(DR),也称为药物重新定位,是一种旨在为现有药物确定新的治疗用途的策略。它提供了一种有效的方法来发现或开发具有新的药理或治疗适应症的药物分子。近年来,制药公司越来越多地在他们的药物发现和开发计划中采用药物再利用策略,从而确定新的生物靶点。与传统的药物发现方法相比,这种策略效率高、节省时间、具有成本效益,并且失败的风险较低。通过最大化现有药物的治疗价值,药物再利用增加了成功的可能性。它是一种有价值的替代方法,可以替代通过传统或新药物发现方法寻找新分子实体(NMEs)的漫长、昂贵和资源密集型过程。药物再利用将基于活性或实验的方法与基于硅或计算的方法相结合,合理地开发或确定药物分子的新用途。它利用现有的人体测试药物的安全性数据,并根据有效的靶分子重新定向其应用。这种方法大有希望,特别是在处理罕见、难以治疗的疾病和被忽视的疾病方面。通过利用丰富的知识和资源,药物再利用为优化现有药物的治疗潜力提供了一种新兴的策略。它提供了一种途径,可以快速确定有效的治疗方法,并将已批准的药物重新用于新的适应症,从而使患者和医疗保健系统都受益。
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