26 results on '"Zhang, Andrew X."'
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2. The Vital Role of Proteomics in Characterizing Novel Protein Degraders
3. ‘Design, synthesis, and strategic use of small chemical probes toward identification of novel targets for drug development’
4. Discovery, Optimization, and Biological Evaluation of Arylpyridones as Cbl-b Inhibitors
5. EFMC – Trends that Link Medicinal Chemistry and Chemical Biology to Translational Drug Discovery
6. Chemical Biology Approaches Confirm MCT4 as the Therapeutic Target of a Cellular Optimized Hit
7. EFMC - trends that link medicinal chemistry and chemical biology to translational drug discovery
8. Antibody-Recruiting Small Molecules: Synthetic Constructs as Immunotherapeutics
9. Affi-BAMS™: A Robust Targeted Proteomics Microarray Platform to Measure Histone Post-Translational Modifications.
10. EFMC: Trends in Medicinal Chemistry and Chemical Biology.
11. Correction to “Design, Synthesis, and Characterization of 4-Aminoquinazolines as Potent Inhibitors of the G Protein-Coupled Receptor Kinase 6 (GRK6) for the Treatment of Multiple Myeloma”
12. Chemical biology approaches to study histone interactors
13. Discovery of 5-{4-[(7-Ethyl-6-oxo-5,6-dihydro-1,5-naphthyridin-3-yl)methyl]piperazin-1-yl}-N-methylpyridine-2-carboxamide (AZD5305): A PARP1–DNA Trapper with High Selectivity for PARP1 over PARP2 and Other PARPs
14. Design, Synthesis, and Characterization of 4-Aminoquinazolines as Potent Inhibitors of the G Protein-Coupled Receptor Kinase 6 (GRK6) for the Treatment of Multiple Myeloma
15. Proteolysis‐targeting chimeras in drug development: A safety perspective
16. Advances in Cellular Target Engagement and Target Deconvolution
17. CETSA beyond Soluble Targets: a Broad Application to Multipass Transmembrane Proteins
18. Chapter Thirteen - Antibody-Recruiting Small Molecules: Synthetic Constructs as Immunotherapeutics
19. Modulating Antibody Structure and Function through Directed Mutations and Chemical Rescue
20. Cover Picture: Target Deconvolution Efforts on Wnt Pathway Screen Reveal Dual Modulation of Oxidative Phosphorylation and SERCA2 (ChemMedChem 12/2017)
21. Target Deconvolution Efforts on Wnt Pathway Screen Reveal Dual Modulation of Oxidative Phosphorylation and SERCA2
22. Limitations and niches of the active targeting approach for nanoparticle drug delivery
23. Advances in Cellular Target Engagement and Target Deconvolution
24. Chemically Synthesized Molecules with the Targeting and Effector Functions of Antibodies
25. Correction to "Design, Synthesis, and Characterization of 4-Aminoquinazolines as Potent Inhibitors of the G Protein-Coupled Receptor Kinase 6 (GRK6) for the Treatment of Multiple Myeloma".
26. Discovery of 6-Fluoro-5-{4-[(5-fluoro-2-methyl-3-oxo-3,4-dihydroquinoxalin-6-yl)methyl]piperazin-1-yl}- N -methylpyridine-2-carboxamide (AZD9574): A CNS-Penetrant, PARP1-Selective Inhibitor.
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