| Literature DB >> 18446518 |
Yue-Zhong Shu1, Benjamin M Johnson, Tian J Yang.
Abstract
Metabolism-related liabilities continue to be a major cause of attrition for drug candidates in clinical development. Such problems may arise from the bioactivation of the parent compound to a reactive metabolite capable of modifying biological materials covalently or engaging in redox-cycling reactions leading to the formation of other toxicants. Alternatively, they may result from the formation of a major metabolite with systemic exposure and adverse pharmacological activity. To avert such problems, biotransformation studies are becoming increasingly important in guiding the refinement of a lead series during drug discovery and in characterizing lead candidates prior to clinical evaluation. This article provides an overview of the methods that are used to uncover metabolism-related liabilities in a pre-clinical setting and offers suggestions for reducing such liabilities via the modification of structural features that are used commonly in drug-like molecules.Mesh:
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Year: 2008 PMID: 18446518 PMCID: PMC2751461 DOI: 10.1208/s12248-008-9016-9
Source DB: PubMed Journal: AAPS J ISSN: 1550-7416 Impact factor: 4.009