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-PLA

Astex Pharmaceuticals
Exploitation of a Novel Binding Pocket in Human Lipoprotein-Associated Phospholipase A2 (Lp-PLA2) Discovered through X-ray Fragment Screening.

Astex Pharmaceuticals
Fragment-Based Discovery of Potent and Selective DDR1/2 Inhibitors.

Astex Pharmaceuticals
Structure-Based Design of Type II Inhibitors Applied to Maternal Embryonic Leucine Zipper Kinase.

Astex Pharmaceuticals
Fragment-based discovery of type I inhibitors of maternal embryonic leucine zipper kinase.

Astex Pharmaceuticals
Fragment-Based Discovery of Allosteric Inhibitors of SH2 Domain-Containing Protein Tyrosine Phosphatase-2 (SHP2).

Astex Pharmaceuticals
Discovery of ASTX029, A Clinical Candidate Which Modulates the Phosphorylation and Catalytic Activity of ERK1/2.

Astex Pharmaceuticals
2-Arylpropionic CXC chemokine receptor 1 (CXCR1) ligands as novel noncompetitive CXCL8 inhibitors.

Domp£
Fragment-Based Discovery of a Potent, Orally Bioavailable Inhibitor That Modulates the Phosphorylation and Catalytic Activity of ERK1/2.

Astex Pharmaceuticals
PARG inhibitory compounds

Cancer Research Technology
Negative allosteric modulators of metabotropic glutamate receptor 3

Vanderbilt University
Treatment of dry eye

Principia Biopharma
Diamide compounds having muscarinic receptor antagonist and β2 adrenergic receptor agonist activity

Theravance Respiratory
Method for the treatment of neurological disorders by enhancing the activity of β-glucocerebrosidase

Amicus Therapeutics
Molecular cloning and characterization of a novel dopamine receptor (D3) as a target for neuroleptics.

U. 109
Design, synthesis, and biological evaluation of conformationally restricted rivastigmine analogues.

University of Bologna
Lead optimization of 7-benzyloxy 2-(4'-pyridylmethyl)thio isoflavone aromatase inhibitors.

Ohio State University
Synthesis and initial SAR studies of 3,6-disubstituted pyrazolo[1,5-a]pyrimidines: a new class of KDR kinase inhibitors.

Merck Research Laboratories