PMID

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Article Title

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Design and synthesis of phenolic hydrazide hydrazones as potent poly(ADP-ribose) glycohydrolase (PARG) inhibitors.

Kumamoto Health Science University

SAR analysis of adenosine diphosphate (hydroxymethyl)pyrrolidinediol inhibition of poly(ADP-ribose) glycohydrolase.

University of Kentucky

Discovery and structure-activity relationships of modified salicylanilides as cell permeable inhibitors of poly(ADP-ribose) glycohydrolase (PARG).

University of Arizona

Biophysical Survey of Small-Molecule ?-Catenin Inhibitors: A Cautionary Tale.

University of Southampton

Structural insights into the active site of poly(ADP-ribose) glycohydrolase using docking modes of 6-hydroxy-3H-xanthen-3-one derivative inhibitors.

Tokyo University of Science

Fluoromethylcyclopropylamine derivatives as potential in vivo toxicophores - A cautionary disclosure.

The University of Manchester

Cell-Active Small Molecule Inhibitors of the DNA-Damage Repair Enzyme Poly(ADP-ribose) Glycohydrolase (PARG): Discovery and Optimization of Orally Bioavailable Quinazolinedione Sulfonamides.

The University of Manchester

X-ray Structures of Target-Ligand Complexes Containing Compounds with Assay Interference Potential.

Rheinische Friedrich-Wilhelms-Universit£T