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• W2034394940 endingPage "544" @default.
• W2034394940 startingPage "544" @default.
• W2034394940 abstract "Phenotype-based screening has been recognized as an important research tool for the discovery of novel therapeutic agents. However, the subsequent identification (ID) of the target of bioactive small molecules has been a major bottleneck in the general application of phenotype-based screening to the drug discovery process. The outcome of conventional target ID methods is significantly influenced by the inherent binding affinity of bioactive small molecules, which can be easily affected by experimental buffer conditions and nonspecific interactions. To overcome these limitations in affinity-based target ID, there has been a community effort to develop new target ID methods. In this review, we focus on the paradigm shift in target ID from noncovalent to covalent bonds and the associated issues in target identification." @default.
• W2034394940 created "2016-06-24" @default.
• W2034394940 creator A5039886122 @default.
• W2034394940 creator A5059282584 @default.
• W2034394940 creator A5091055050 @default.
• W2034394940 date "2013-01-01" @default.
• W2034394940 modified "2023-10-18" @default.
• W2034394940 title "From noncovalent to covalent bonds: a paradigm shift in target protein identification" @default.
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• W2034394940 doi "https://doi.org/10.1039/c2mb25502b" @default.
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