25 results on '"Holl, Ralph"'
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2. Synthesis, biological evaluation, and molecular docking studies of deoxygenated C-glycosides as LpxC inhibitors
3. Antibacterial activity of xylose-derived LpxC inhibitors – Synthesis, biological evaluation and molecular docking studies
4. Bioactive pyrrole-based compounds with target selectivity
5. Pyrrolidine in Drug Discovery: A Versatile Scaffold for Novel Biologically Active Compounds
6. Editorial: Emerging heterocycles as bioactive compounds
7. Chiral pool synthesis and biological evaluation of C-furanosidic and acyclic LpxC inhibitors
8. Synthesis and biological evaluation of enantiomerically pure glyceric acid derivatives as LpxC inhibitors
9. Synthesis and biological evaluation of C-ethynyl furanosides as LpxC inhibitors
10. C-Triazolyl β-d-furanosides as LpxC inhibitors: stereoselective synthesis and biological evaluation
11. Synthesis, Biological Evaluation, and Molecular Docking Studies of Aldotetronic Acid-Based LpxC Inhibitors
12. Synthesis and biological evaluation of triazolyl-substituted benzyloxyacetohydroxamic acids as LpxC inhibitors
13. Front Cover: Structure‐Based Design, Synthesis, and Biological Evaluation of Triazole‐Based smHDAC8 Inhibitors (ChemMedChem 7/2020)
14. Structure‐Based Design, Synthesis, and Biological Evaluation of Triazole‐Based smHDAC8 Inhibitors
15. Proline-based hydroxamates targeting the zinc-dependent deacetylase LpxC: Synthesis, antibacterial properties, and docking studies
16. Chiral Pool Synthesis, Biological Evaluation and Molecular Docking Studies ofC‐Furanosidic LpxC Inhibitors
17. Phenylethylene glycol-derived LpxC inhibitors with diverse Zn2+-binding groups
18. Characterization of Histone Deacetylase 8 (HDAC8) Selective Inhibition Reveals Specific Active Site Structural and Functional Determinants
19. LpxC inhibitors: a patent review (2010-2016)
20. Novel Potent Proline-Based Metalloproteinase Inhibitors: Design, (Radio)Synthesis, and First in Vivo Evaluation as Radiotracers for Positron Emission Tomography
21. Chiral Pool Synthesis, Biological Evaluation and Molecular Docking Studies of C‐Furanosidic LpxC Inhibitors.
22. Insights into the Zinc-Dependent Deacetylase LpxC: Biochemical Properties and Inhibitor Design
23. Synthesis, biological evaluation, and molecular docking studies of aldotetronic acid-based LpxC inhibitors
24. Bioactive pyrrole-based compounds with target selectivity
25. Insights into the Zinc-Dependent Deacetylase LpxC: Biochemical Properties and Inhibitor Design.
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