Critical review of the role of HTS in drug discovery.
By R. Macarron. 2006
234 citations recorded by the source corpus.
Subfields: Computational Theory and Mathematics, Economics and Econometrics, Reproductive Medicine
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Citations in the corpus
- Novel trends in high-throughput screening. (2009, unknown): “Novel processes for lead discovery Screening of chemical libraries via the processes of HTS and uHTS is a relatively new discipline that started about 10–15 years ago [5 ,6] with initial attempts to screen collections of natural products/extracts [20].”
- The ToxCast program for prioritizing toxicity testing of environmental chemicals. (2007, background): “Thus, the primary driver transforming drug discovery has been HTS technologies (Macarron, 2006).”
- A decade of fragment-based drug design: strategic advances and lessons learned (2007, background): “To improve the chances of finding agents that are active against these targets, technologies such as combinatorial chemistry and ultra-high-throughput screening (HTS) approaches have considerably expanded the numbers of compounds that can be evaluated for their biological activit”