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- W2090863707 endingPage "1969" @default.
- W2090863707 startingPage "1964" @default.
- W2090863707 abstract "Modern drug discovery often involves screening small molecules for their ability to bind to a preselected protein target. Target-oriented syntheses of these small molecules, individually or as collections (focused libraries), can be planned effectively with retrosynthetic analysis. Drug discovery can also involve screening small molecules for their ability to modulate a biological pathway in cells or organisms, without regard for any particular protein target. This process is likely to benefit in the future from an evolving forward analysis of synthetic pathways, used in diversity-oriented synthesis, that leads to structurally complex and diverse small molecules. One goal of diversity-oriented syntheses is to synthesize efficiently a collection of small molecules capable of perturbing any disease-related biological pathway, leading eventually to the identification of therapeutic protein targets capable of being modulated by small molecules. Several synthetic planning principles for diversity-oriented synthesis and their role in the drug discovery process are presented in this review." @default.
- W2090863707 created "2016-06-24" @default.
- W2090863707 creator A5035618234 @default.
- W2090863707 date "2000-03-17" @default.
- W2090863707 modified "2023-10-18" @default.
- W2090863707 title "Target-Oriented and Diversity-Oriented Organic Synthesis in Drug Discovery" @default.
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- W2090863707 doi "https://doi.org/10.1126/science.287.5460.1964" @default.
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