16 articles for thisTarget
              
              The following articles (labelled with PubMed ID or TBD) are for your review
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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
 
New Horizons of Synthetic Lethality in Cancer: Current Development and Future Perspectives.

University of Bologna
 
Biophysical Survey of Small-Molecule β-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.

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.

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

Rheinische Friedrich-Wilhelms-Universit£T
 
[1,2,4]triazolo[1,5-a]pyridine compound as JAK inhibitor and use thereof

Zhuhai United Laboratories Co.
 
NOVEL COMPOUNDS AS HISTONE DEACETYLASE 6 INHIBITOR, AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME

Chong Kun Dang Pharmaceutical
 
Substituted pyrazlo[3,4-c]pyridines as selective BTK kinase inhibitors

Jumbo Drug Bank
 
Substituted thiohydantoin derivatives as androgen receptor antagonists

Janssen Pharmaceutica
 
Screening of drugs by FRET analysis identifies inhibitors of SARS-CoV 3CL protease.

National Taiwan University
 
Oxamic acid analogues as LDH-C4-specific competitive inhibitors.

Instituto Politécnico Nacional
 
Thiolactomycin-based ß-Ketoacyl-AcpM Synthase A (KasA) Inhibitors: FRAGMENT-BASED INHIBITOR DISCOVERY USING TRANSIENT ONE-DIMENSIONAL NUCLEAR OVERHAUSER EFFECT NMR SPECTROSCOPY.

Institute For Chemical Biology & Drug Discovery