书目名称 | Optimization in Drug Discovery | 编辑 | Zhengyin Yan,Gary W. Caldwell | 视频video | | 概述 | Includes supplementary material: | 丛书名称 | Methods in Pharmacology and Toxicology | 图书封面 |  | 描述 | Recent analyses of drug attrition rates reveal that a significant number of drug candidates fail in the later stage of clinical development owing to absorption, distribution, metabolism, elimination (ADME), and toxicity issues. Lead optimization in drug discovery, a process attempting to uncover and correct these defects of drug candidates, is highly beneficial in lowering the cost and time to develop therapeutic drugs by reducing drug candidate failures in development. At present, parallel synthesis combining with high-throughput screening has made it easier to generate highly potent compounds (i. e. , hits). However, to be a potential drug, a hit must have drug-like characteristics in addition to potency, which include optimal physicochemical properties, reasonable ph- macokinetic parameters, and good safety profiles. Therefore, research tools must be available in drug discovery to rapidly screen for compounds with favorable drug-like properties, and thus adequate resources can be directed to projects with high potential. Optimization in Drug Discovery: In Vitro Methods is a compilation of detailed experimental protocols necessary for setting up a variety of assays important in c | 出版日期 | Book 2004 | 版次 | 1 | doi | https://doi.org/10.1385/1592598005 | isbn_softcover | 978-1-61737-499-9 | isbn_ebook | 978-1-59259-800-7Series ISSN 1557-2153 Series E-ISSN 1940-6053 | issn_series | 1557-2153 | copyright | Humana Press 2004 |
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