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21 articles for SD Kattar


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

PMID
Data
Article Title
Organization
Discovery of a chemical probe for PRDM9.EBI
University of Toronto
Discovery and Optimization of N-Heteroaryl Indazole LRRK2 Inhibitors.EBI
Merck & Co.
Discovery of MK-1468: A Potent, Kinome-Selective, Brain-Penetrant Amidoisoquinoline LRRK2 Inhibitor for the Potential Treatment of Parkinson's Disease.EBI
Merck
Optimization of brain-penetrant picolinamide derived leucine-rich repeat kinase 2 (LRRK2) inhibitors.EBI
Merck
Structure-Guided Discovery of Aminoquinazolines as Brain-Penetrant and Selective LRRK2 Inhibitors.EBI
Merck
Discovery of a new series of PI3K-δ inhibitors from Virtual Screening.EBI
Merck
Design of selective PI3Kδ inhibitors using an iterative scaffold-hopping workflow.EBI
Merck
Structure Overhaul Affords a Potent Purine PI3Kδ Inhibitor with Improved Tolerability.EBI
TBA
Piperazinyl pyrimidine derivatives as potent gamma-secretase modulators.EBI
Merck Research Laboratories
AMP-activated protein kinase inhibitors and methods of making and using the sameBDB
University Of Colorado
HETEROBIFUNCTIONAL TARGETED PROTEIN DEGRADERSBDB
St. Jude Children'S Research Hospital
ARYLCYCLOHEXYLAMINE DERIVATIVES AND THEIR USE IN THE TREATMENT OF PSYCHIATRIC DISORDERSBDB
Gilgamesh Pharmaceuticals
Six-membered ring benzo derivatives as DPP-4 inhibitor and use thereofBDB
East China University of Science and Technology
Aminoindazole derivatives as sodium channel inhibitorsBDB
Almirall
Iminothiadiazine dioxides containing a thioamide, amidine, or amide oxime group as BACE inhibitors, compositions, and their useBDB
Merck Sharp & Dohme
Substituted phenylimidazopyrazoles and their useBDB
Bayer Pharma Aktiengesellschaft
Substituted 5-(3,5-dimethylisoxazol-4-yl)indoline-2-onesBDB
Beigene
Amide, urea or sulfone amide linked benzothiazole inhibitors of endothelial lipaseBDB
Bristol-Myers Squibb
N-biarylamidesBDB
Bayer Intellectual Property
Design, Synthesis, Structural Characterization by IR, (1) H, (13) C, (15) N, 2D-NMR, X-Ray Diffraction and Evaluation of a New Class of Phenylaminoacetic Acid Benzylidene Hydrazines as pfENR Inhibitors.BDB
Bombay College of Pharmacy
Tetrahydrothienopyridylbutyl-tetrahydrobenzindoles: new selective ligands of the 5-HT(7) receptor.BDB
Meiji Seika Kaisha