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Titlebook: Chemical Genomics; Small Molecule Probe S. Jaroch,H. Weinmann Conference proceedings 2006 Springer-Verlag Berlin Heidelberg 2006 Chemical b

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21#
發(fā)表于 2025-3-25 07:16:44 | 只看該作者
22#
發(fā)表于 2025-3-25 10:39:01 | 只看該作者
23#
發(fā)表于 2025-3-25 13:19:37 | 只看該作者
Chemical Genomics978-3-540-37635-4Series ISSN 0947-6075
24#
發(fā)表于 2025-3-25 18:21:48 | 只看該作者
Gasstoffwechsel und Elektrolyte,et and ligand clusters are linked by generating binding affinity profiles of chemotypes vs a target panel. The application of this multidimensional similarity paradigm will be described in the context of Lead Generation to identify novel chemical hit classes for G-protein coupled receptors.
25#
發(fā)表于 2025-3-25 23:44:53 | 只看該作者
26#
發(fā)表于 2025-3-26 02:52:23 | 只看該作者
Chemogenomics Strategies for G-Protein Coupled Receptor Hit Finding,et and ligand clusters are linked by generating binding affinity profiles of chemotypes vs a target panel. The application of this multidimensional similarity paradigm will be described in the context of Lead Generation to identify novel chemical hit classes for G-protein coupled receptors.
27#
發(fā)表于 2025-3-26 06:44:33 | 只看該作者
Probing Protein Function with Small Molecules, is providing the chemical means to understand biological systems not easily accessible using classical genetic manipulations. In this article, we will discuss how natural product mode of action studies and novel bio-organic manipulation of intracellular protein levels are proving useful in the exploration of cell biology.
28#
發(fā)表于 2025-3-26 10:27:52 | 只看該作者
Gasstoffwechsel und Elektrolyte,tructures” has been defined for scaffolds, such as the benzodiazepines, which very often produce biologically active analogs in a target family, in this case in the class of G-protein-coupled receptors. The SOSA approach is a strategy to modify the selectivity of biologically active compounds, gener
29#
發(fā)表于 2025-3-26 15:15:52 | 只看該作者
Probleme der Intensivbehandlungds (termed chemoprints) are identified using homology modeling, molecular docking, and experimental profiling. These chemoprints can support the design and synthesis of compound libraries tailor-made for a novel GPCR target.
30#
發(fā)表于 2025-3-26 17:19:27 | 只看該作者
https://doi.org/10.1007/978-3-642-72296-7eadout for very high data quality. SpeedScreen is a highly miniaturized and automated screening system for high-throughput affinity-selection of compounds. In practice, pools of compounds are incubated with the target protein and the unbound chemical compounds are removed from the target-compound co
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