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19 articles for V Berdini


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Fragment-Based Approach to the Development of an Orally Bioavailable Lactam Inhibitor of Lipoprotein-Associated Phospholipase A2 (Lp-PLAEBI
Astex Pharmaceuticals
Exploitation of a Novel Binding Pocket in Human Lipoprotein-Associated Phospholipase A2 (Lp-PLA2) Discovered through X-ray Fragment Screening.EBI
Astex Pharmaceuticals
Fragment-Based Discovery of Potent and Selective DDR1/2 Inhibitors.EBI
Astex Pharmaceuticals
Structure-Based Design of Type II Inhibitors Applied to Maternal Embryonic Leucine Zipper Kinase.EBI
Astex Pharmaceuticals
Fragment-based discovery of type I inhibitors of maternal embryonic leucine zipper kinase.EBI
Astex Pharmaceuticals
Fragment-Based Discovery of Allosteric Inhibitors of SH2 Domain-Containing Protein Tyrosine Phosphatase-2 (SHP2).EBI
Astex Pharmaceuticals
Discovery of ASTX029, A Clinical Candidate Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2.EBI
Astex Pharmaceuticals
2-Arylpropionic CXC chemokine receptor 1 (CXCR1) ligands as novel noncompetitive CXCL8 inhibitors.EBI
Domp£
Fragment-Based Discovery of a Potent, Orally Bioavailable Inhibitor That Modulates the Phosphorylation and Catalytic Activity of ERK1/2.EBI
Astex Pharmaceuticals
PARG inhibitory compoundsBDB
Cancer Research Technology
Negative allosteric modulators of metabotropic glutamate receptor 3BDB
Vanderbilt University
Treatment of dry eyeBDB
Principia Biopharma
Diamide compounds having muscarinic receptor antagonist and β2 adrenergic receptor agonist activityBDB
Theravance Respiratory
Method for the treatment of neurological disorders by enhancing the activity of β-glucocerebrosidaseBDB
Amicus Therapeutics
Molecular cloning and characterization of a novel dopamine receptor (D3) as a target for neuroleptics.BDB
U. 109
Design, synthesis, and biological evaluation of conformationally restricted rivastigmine analogues.BDB
University of Bologna
Lead optimization of 7-benzyloxy 2-(4'-pyridylmethyl)thio isoflavone aromatase inhibitors.BDB
Ohio State University
Synthesis and initial SAR studies of 3,6-disubstituted pyrazolo[1,5-a]pyrimidines: a new class of KDR kinase inhibitors.BDB
Merck Research Laboratories