Multi-Step Usage of in Vivo Models During Rational Drug Design and Discovery

被引:47
作者
Williams, Charles H. [1 ]
Hong, Charles C. [1 ,2 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Med, Div Cardiovasc Med, Nashville, TN 37232 USA
[2] Vet Affairs TVHS, Nashville, TN 37212 USA
关键词
phenotypic screen; drug discovery; small molecules; drug design chemical genetics; model organisms; SMALL-MOLECULE SCREEN; CAENORHABDITIS-ELEGANS; TARGET IDENTIFICATION; ALZHEIMERS-DISEASE; C-ELEGANS; ZEBRAFISH; DROSOPHILA; SYSTEM; CANCER; DIFFERENTIATION;
D O I
10.3390/ijms12042262
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
In this article we propose a systematic development method for rational drug design while reviewing paradigms in industry, emerging techniques and technologies in the field. Although the process of drug development today has been accelerated by emergence of computational methodologies, it is a herculean challenge requiring exorbitant resources; and often fails to yield clinically viable results. The current paradigm of target based drug design is often misguided and tends to yield compounds that have poor absorption, distribution, metabolism, and excretion, toxicology (ADMET) properties. Therefore, an in vivo organism based approach allowing for a multidisciplinary inquiry into potent and selective molecules is an excellent place to begin rational drug design. We will review how organisms like the zebrafish and Caenorhabditis elegans can not only be starting points, but can be used at various steps of the drug development process from target identification to pre-clinical trial models. This systems biology based approach paired with the power of computational biology; genetics and developmental biology provide a methodological framework to avoid the pitfalls of traditional target based drug design.
引用
收藏
页码:2262 / 2274
页数:13
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