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4-Arylazo-3, 5-Diamino-1h-Pyrazole CDK Inhibitors: SAR Study, Crystal Structure in Complex With CDK2, Selectivity, and Cellular Effects
Discovery of a New Class of Highly Potent Inhibitors of Acid Ceramidase: Synthesis and Structure–Activity Relationship (SAR)
Journal of Medicinal Chemistry
Drug Discovery
Molecular Medicine
Structure?activity Relationships of Amyloid Beta-Aggregation Inhibitors Based on Curcumin: Influence of Linker Length and Flexibility
Chemical Biology and Drug Design
Biochemistry
Organic Chemistry
Drug Discovery
Molecular Medicine
Pharmacology
Insilico Discovery of Human Aurora B Kinase Inhibitors by Molecular Docking, Pharmacophore Validation and Admet Studies
Asian Journal of Pharmaceutical and Clinical Research
Pharmacology
Pharmaceutical Science
Anaplastic Lymphoma Kinase Confers Resistance to BRAF Kinase Inhibitors in Melanoma
iScience
Multidisciplinary
Development of Selective Covalent Janus Kinase 3 Inhibitors
Journal of Medicinal Chemistry
Drug Discovery
Molecular Medicine
Regulation of Casein Kinase-2 (CK2) Activity by Inositol Phosphates
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Structural Differences Between Wild-Type and Double Mutant EGFR Modulated by Third-Generation Kinase Inhibitors
Journal of the American Chemical Society
Biochemistry
Colloid
Catalysis
Chemistry
Surface Chemistry
Effects of Tyrosine Kinase and Phosphatase Inhibitors on Mitosis Progression in Synchronized Tobacco BY-2 Cells
Cytology and Genetics
Genetics
Histology
Frontispiz: The Interplay Between Structure and Product Selectivity of CO2 Hydrogenation
Angewandte Chemie
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