25 results on '"Wegert, Anita"'
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2. Front Cover: (R)‐PFI‐2 Analogues as Substrates and Inhibitors of Histone Lysine Methyltransferase SETD7 (ChemMedChem 23/2023)
3. Towards Multitargeted Ligands as Pain Therapeutics: Dual Ligands of the Cavα2δ‐1 Subunit of Voltage‐Gated Calcium Channel and the μ‐Opioid Receptor.
4. (R)‐PFI‐2 Analogues as Substrates and Inhibitors of Histone Lysine Methyltransferase SETD7
5. Examining sterically demanding lysine analogs for histone lysine methyltransferase catalysis
6. Data from The Tankyrase Inhibitor OM-153 Demonstrates Antitumor Efficacy and a Therapeutic Window in Mouse Models
7. Supplementary Figures S1-S8 from The Tankyrase Inhibitor OM-153 Demonstrates Antitumor Efficacy and a Therapeutic Window in Mouse Models
8. Abstract 2651: The tankyrase inhibitor OM-153 demonstrates anti-tumor effect with a therapeutic index above 10
9. The Tankyrase Inhibitor OM-153 Demonstrates Antitumor Efficacy and a Therapeutic Window in Mouse Models
10. Development of a 1,2,4-Triazole-Based Lead Tankyrase Inhibitor: Part II
11. Methylation of geometrically constrained lysine analogues by histone lysine methyltransferases
12. Chlorodifluoromethyl-substituted monosaccharide derivatives—radical activation of the carbon–chlorine-bond
13. Novel SAR for quinazoline inhibitors of EHMT1 and EHMT2
14. Preclinical Lead Optimization of a 1,2,4-Triazole Based Tankyrase Inhibitor
15. Methylation of geometrically constrained lysine analogues by histone lysine methyltransferases
16. Structure-Activity Relationship Studies on (R)-PFI-2 Analogues as Inhibitors of Histone Lysine Methyltransferase SETD7
17. Structure-Activity Relationship Studies on (R)-PFI-2 Analogues as Inhibitors of Histone Lysine Methyltransferase SETD7
18. Quantitative Assessment of Drug Delivery to Tissues and Association with Phospholipidosis : A Case Study with Two Structurally Related Diamines in Development
19. Quantitative Assessment of Drug Delivery to Tissues and Association with Phospholipidosis: A Case Study with Two Structurally Related Diamines in Development
20. Design and Synthesis of Enantiomerically Pure Decahydroquinoxalines as Potent and Selective κ-Opioid Receptor Agonists with Anti-Inflammatory Activityin Vivo
21. Novel Epigenetic Enzyme Inhibitors for HKMT's by Pursuing a Target Family-Centric Library Approach Histone-site inhibitors SAM-site inhibitors
22. Design and Synthesis of Enantiomerically Pure Decahydroquinoxalines as Potent and Selective κ-Opioid Receptor Agonists with Anti-Inflammatory Activity in Vivo.
23. Organofluorine Compounds and Fluorinating Agents, Part 33:Regioselective Chlorodifluoromethylations in the 1-Position of 1,2-Unsaturated Monosaccharide Derivatives
24. Synthesis of 2,3- or 1,2-unsaturated derivatives of 2-deoxy-2-trifluoromethylhexopyranoses
25. Towards Multitargeted Ligands as Pain Therapeutics: Dual Ligands of the Ca v α2δ-1 Subunit of Voltage-Gated Calcium Channel and the μ-Opioid Receptor.
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