An Overview of Aflat Neurological Diseases and Drug Discovery: An Overview

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Abstract

Hundreds of millions of people worldwide are af ected by neurological disorders. More than 50 million people have epilepsy; 7.7 million new dementia cases are reported every year worldwide. Over the last decade, fewer new drugs for nervous system disorders have garnered approval in comparison to other therapeutic areas. An important step of the drug development process is the lead identification and lead optimization to develop the best pharmacokinetic profile for the desired formulation and preferred route of administration. It requires Quantitative Structure-Activity Relationship (QSAR) to understand which modifications will best enhance af inity. Computer-aided molecular design (CAMD) is used in innovative strategies assisting in improving the binding af inities of drug candidates to specific receptors. Single-photon emission computed tomography (SPECT) and positron emission tomography (PET) have proven to be useful in phases ranging from preclinical development to the initial stages of clinical testing. The high sensitivity of these imaging modalities makes them particularly suited for exploratory investigational new drug development.
平坦神经系统疾病和药物发现综述
全世界有数亿人受到神经系统疾病的影响。5000多万人患有癫痫;全世界每年报告770万例新的痴呆症病例。在过去十年中,与其他治疗领域相比,神经系统疾病的新药获得批准的较少。药物开发过程中的一个重要步骤是先导物识别和先导物优化,从而为所需的配方和首选给药途径开发最佳药代动力学特征。它需要定量构效关系(Quantitative Structure-Activity Relationship, QSAR)来了解哪些修饰能最好地增强亲和力。计算机辅助分子设计(CAMD)被用于创新策略,以帮助提高候选药物与特定受体的结合亲和力。单光子发射计算机断层扫描(SPECT)和正电子发射断层扫描(PET)已被证明在从临床前开发到临床测试的初始阶段都是有用的。这些成像方式的高灵敏度使它们特别适合于探索性研究新药开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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