Literature DB >> 15183334

Applications of high-throughput ADME in drug discovery.

Daniel B Kassel1.   

Abstract

Assessment of physicochemical and pharmacological properties is now conducted at very early stages of drug discovery for the purpose of accelerating the conversion of hits and leads into qualified development candidates. In particular, in vitro absorption, distribution, metabolism and elimination (ADME) assays and in vivo drug metabolism pharmacokinetic (DMPK) studies are being conducted throughout the discovery process, from hit generation through to lead optimization, with the goal of reducing the attrition rate of these potential drug candidates as they progress through development. Because the continuing trend in drug discovery has been to access ADME information earlier and earlier in the discovery process, the need has arisen within the analytical community to introduce faster and better analytical methods to enhance the 'developability' of drug leads. Strategies for streamlined ADME assessment of drug candidates in discovery and pre-clinical development are presented within.

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Year:  2004        PMID: 15183334     DOI: 10.1016/j.cbpa.2004.04.015

Source DB:  PubMed          Journal:  Curr Opin Chem Biol        ISSN: 1367-5931            Impact factor:   8.822


  10 in total

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Authors:  Sunetra Ray; Peter B Madrid; Paul Catz; Susanna E LeValley; Michael J Furniss; Linda L Rausch; R Kiplin Guy; Joseph L DeRisi; Lalitha V Iyer; Carol E Green; Jon C Mirsalis
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Review 3.  Drug discovery effectiveness from the standpoint of therapeutic mechanisms and indications.

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Authors:  Maria A Miteva; Stephanie Violas; Matthieu Montes; David Gomez; Pierre Tuffery; Bruno O Villoutreix
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7.  Pharmacoinformatics approach for investigation of alternative potential hepatitis C virus nonstructural protein 5B inhibitors.

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Review 8.  Current status and future directions of high-throughput ADME screening in drug discovery.

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Journal:  J Pharm Anal       Date:  2020-05-23

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10.  Synthesis, Molecular Structure, Metabolic Stability and QSAR Studies of a Novel Series of Anticancer N-Acylbenzenesulfonamides.

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Journal:  Molecules       Date:  2015-10-21       Impact factor: 4.411

  10 in total

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