Remove Pharmaceuticals Remove Production Remove Screening Hits
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Target-directed cancer: protein-ligand interactions  

Drug Target Review

The team that I lead within the CCDD is called the Hit Discovery and Structural Design Team. We support the drug discovery projects of the CCDD with assay development and screening, biophysics, structural biology and recombinant protein production.

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We Need Better Benchmarks for Machine Learning in Drug Discovery

Practical Cheminformatics

Most pharmaceutical compounds tend to have solubilities somewhere between 1 and 500 µM. It is quite a bit more potent than the values one finds with screening hits, which typically have IC50s in the single to double-digit µM range. Many have suggested that pharmaceutical companies should open more of their data to the community.

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