Journal
NATURE CHEMICAL BIOLOGY
Volume 5, Issue 5, Pages 274-275Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/nchembio0509-274
Keywords
-
Categories
Ask authors/readers for more resources
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.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available