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Fragment-based drug discovery takes a virtual turn

Journal

NATURE CHEMICAL BIOLOGY
Volume 5, Issue 5, Pages 274-275

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nchembio0509-274

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In the realm of modern drug discovery technologies, fragment-based approaches and virtual ligand screening are emerging alternative approaches to high-throughput screening (HTS). For as simple as it sounds, a hybrid approach in which fragments are discovered first in silico may be an unbeatable route to hit identification for some drug targets.

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