Abstract

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.

Highlights

  • Cancer, Alzheimer, diabetes; all are leading causes of death in the US

  • Unlike exogenous factors like HIV/AIDS and influenza, they are the result of endogenous developmental programming behaving in an aberrant fashion

  • Even if all exogenous infections were obliterated from the face of the globe we would still face these diseases

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Summary

Introduction

Alzheimer, diabetes; all are leading causes of death in the US. Unlike exogenous factors like HIV/AIDS and influenza, they are the result of endogenous developmental programming behaving in an aberrant fashion. The average time it takes a drug to reach the bedside from discovery is 12 years, and a single pharmaceutical agent costs from 500 million to 2 billion dollars to bring to market [3]. X-ray crystallography and computer aided design [5] Most of these target centric designs often fail to meet the standard when ADMET (absorption, digestion, metabolism and toxicity) is evaluated after years of research and millions of dollars. In place of this paradigm, a systems biology approach is emerging using a phenotypic screen that inherently takes into account certain ADMET properties. The following article will present a systematized development method for rational drug design based on phenotype driven discovery

Workflow
Organismal Models
Target Identification
SAR and Compound Optimization
Vertebrate Toxicity
Afterword
49. FDA ICH Guidance for industry
Findings
Methods

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