| Química Nova | |
| SYNTHETIC STRATEGIES IN DRUG DISCOVERY: EMPLOYNG DIVERSITY-ORIENTED SYNTHESIS | |
| Sangi, Diego Pereira1  Universidade Federal Fluminense, Volta Redonda, Brazil1  | |
| 关键词: Â target oriented synthesis; diversity oriented synthesis; drug discovery; | |
| DOI : 10.5935/0100-4042.20160089 | |
| 学科分类:化学(综合) | |
| 来源: Sociedade Brasileira de Quimica | |
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【 摘 要 】
Drug discovery often involves screening synthetic small molecules for their ability to bind to a macromolecular target. Target-Oriented Synthesis of a specific compound or a focused library can be planned combining retrosynthetic analysis and rational drug design. Biologically active molecules also can be identified through the unfocused screening of compound libraries. Diversity-Oriented Synthesis (DOS) emerges as an excellent strategy that leads to a library of structurally complex and diverse small molecules, covering a larger chemical space and increasing the probability of identifying modulators.
【 授权许可】
Unknown
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO201912050596754ZK.pdf | 629KB |
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