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Pharmacophore Based Drug Design Approach as a Practical Process in Drug Discovery

机译:基于药物的药物设计方法作为药物发现的实际过程

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This review summarizes the background and updated progress of pharmacophore based drug design and provides the fundamental approach strategies on both structure based and ligand based pharmacophore approaches. The different programs and methodologies enable the implementation of more accurate and sophisticated pharmacophore model generation and application in drug discovery. This review will discuss and illustrate their advantages in pharmacophore based virtual screening and exemplify the detailed application workflow, which can be easily utilized by pharmaceutical bench work medicinal chemists. Pharmacophore based drug design process includes pharmacophore modeling and validation; pharmacophore based virtual screening, virtual hits profiling and lead identification. Strategies and proven methodologies for pharmacophore modeling are described including common feature and 3D QSAR based pharmacophore generation as well as structure based pharmacophore development. Different virtual screening strategies will be described in this review with detailed case studies for supporting practical applications. Representative success examples of pharmacophore based virtual screening for lead generation will be collected to demonstrate capabilities.
机译:本文总结的背景下,基于药效的药物设计的最新进展,并提供了两种结构基础和配体基于药效接近的根本途径策略。不同的程序和方法,实现更精确和复杂的药效模型生成和应用在药物开发领域的实施。本次审查将讨论和说明基于药效的虚拟筛选自身优势,举例说明详细的应用流程,可以通过药物钳工工作药物化学家很容易地利用。基于药效的药物设计方法包括药效建模和验证;基于药效团虚拟筛选,虚拟命中剖析和铅鉴定。战略和先进成熟的药效建模描述,包括共同的特征和基于3D QSAR药效代以及基于结构的药效发展。不同的虚拟筛选策略将在这次审查与支持实际应用详细的个案研究来说明。铅代药效基于虚拟筛选的代表性成功的例子,将收集来证明能力。

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