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A fragment-like approach to PYCR1 inhibition

Kirsty Milne1, Jianhui Sun2, Esther A Zaal3

  • 1Department of Pure and Applied Chemistry, Thomas Graham Building, University of Strathclyde, Glasgow G1 1XL, United Kingdom.

Bioorganic & Medicinal Chemistry Letters
|August 1, 2019
PubMed

Keywords:
Fragment-based drug discoveryInhibitorOncologyProline modulationTool compound

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