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ADDME – Avoiding Drug Development Mistakes Early: central nervous system drug discovery perspective

The advent of early absorption, distribution, metabolism, excretion, and toxicity (ADMET) screening has increased the attrition rate of weak drug candidates early in the drug-discovery process, and decreased the proportion of compounds failing in clinical trials for ADMET reasons. This paper reviews...

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Detalles Bibliográficos
Autores principales: Tsaioun, Katya, Bottlaender, Michel, Mabondzo, Aloise
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2697629/
https://www.ncbi.nlm.nih.gov/pubmed/19534730
http://dx.doi.org/10.1186/1471-2377-9-S1-S1
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author Tsaioun, Katya
Bottlaender, Michel
Mabondzo, Aloise
author_facet Tsaioun, Katya
Bottlaender, Michel
Mabondzo, Aloise
author_sort Tsaioun, Katya
collection PubMed
description The advent of early absorption, distribution, metabolism, excretion, and toxicity (ADMET) screening has increased the attrition rate of weak drug candidates early in the drug-discovery process, and decreased the proportion of compounds failing in clinical trials for ADMET reasons. This paper reviews the history of ADMET screening and its place in pharmaceutical development, and central nervous system drug discovery in particular. Assays that have been developed in response to specific needs and improvements in technology that result in higher throughput and greater accuracy of prediction of human mechanisms of absorption and toxicity are discussed. The paper concludes with the authors' forecast of new models that will better predict human efficacy and toxicity.
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spelling pubmed-26976292009-06-16 ADDME – Avoiding Drug Development Mistakes Early: central nervous system drug discovery perspective Tsaioun, Katya Bottlaender, Michel Mabondzo, Aloise BMC Neurol Proceedings The advent of early absorption, distribution, metabolism, excretion, and toxicity (ADMET) screening has increased the attrition rate of weak drug candidates early in the drug-discovery process, and decreased the proportion of compounds failing in clinical trials for ADMET reasons. This paper reviews the history of ADMET screening and its place in pharmaceutical development, and central nervous system drug discovery in particular. Assays that have been developed in response to specific needs and improvements in technology that result in higher throughput and greater accuracy of prediction of human mechanisms of absorption and toxicity are discussed. The paper concludes with the authors' forecast of new models that will better predict human efficacy and toxicity. BioMed Central 2009-06-12 /pmc/articles/PMC2697629/ /pubmed/19534730 http://dx.doi.org/10.1186/1471-2377-9-S1-S1 Text en Copyright © 2009 Tsaioun et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Proceedings
Tsaioun, Katya
Bottlaender, Michel
Mabondzo, Aloise
ADDME – Avoiding Drug Development Mistakes Early: central nervous system drug discovery perspective
title ADDME – Avoiding Drug Development Mistakes Early: central nervous system drug discovery perspective
title_full ADDME – Avoiding Drug Development Mistakes Early: central nervous system drug discovery perspective
title_fullStr ADDME – Avoiding Drug Development Mistakes Early: central nervous system drug discovery perspective
title_full_unstemmed ADDME – Avoiding Drug Development Mistakes Early: central nervous system drug discovery perspective
title_short ADDME – Avoiding Drug Development Mistakes Early: central nervous system drug discovery perspective
title_sort addme – avoiding drug development mistakes early: central nervous system drug discovery perspective
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2697629/
https://www.ncbi.nlm.nih.gov/pubmed/19534730
http://dx.doi.org/10.1186/1471-2377-9-S1-S1
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