44 results on '"Stellfeld, Timo"'
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2. Discovery and characterization of orally bioavailable 4-chloro-6-fluoroisophthalamides as covalent PPARG inverse-agonists
3. Correction to “Discovery and Structure-Based Design of Potent Covalent PPARγ Inverse-Agonists BAY-4931 and BAY-0069”
4. Discovery and Structure-Based Design of Potent Covalent PPARγ Inverse-Agonists BAY-4931 and BAY-0069
5. Asymmetric Total Synthesis of Complex Marine Natural Products
6. Rational Design and Synthesis of Selective PRMT4 Inhibitors: A New Chemotype for Development of Cancer Therapeutics**
7. Rational Design and Synthesis of Selective PRMT4 Inhibitors: a New Chemotype for Development of Cancer Therapeutics
8. Potent and Selective Human Prostaglandin F (FP) Receptor Antagonist (BAY-6672) for the Treatment of Idiopathic Pulmonary Fibrosis (IPF)
9. Asymmetric Total Synthesis of Complex Marine Natural Products
10. Abstract 2: Discovery of BAY 2402234 by phenotypic screening: A human Dihydroorotate Dehydrogenase (DHODH) inhibitor in clinical trials for the treatment of myeloid malignancies
11. Abstract DDT02-04: BAY 2402234: A novel, selective dihydroorotate dehydrogenase (DHODH) inhibitor for the treatment of myeloid malignancies
12. Abstract 5239: Probing the cancer epigenome: empowering target validation by open innovation
13. Abstract A44: Coordination of stress signals by the lysine methyltransferase SMYD2 promotes pancreatic cancer
14. Abstract 4475: SMYD2 inhibitor BAY-598 reveals the giant scaffold AHNAK as a novel multi-methylated substrate
15. Discovery and Characterization of a Highly Potent and Selective Aminopyrazoline-Based in Vivo Probe (BAY-598) for the Protein Lysine Methyltransferase SMYD2
16. Coordination of stress signals by the lysine methyltransferase SMYD2 promotes pancreatic cancer
17. Abstract 2829: Discovery and in vitro and in vivo characterization of aminopyrazoline-based SMYD2 inhibitors
18. Zur Synthese von Hexacyclinsäure
19. Gene expression levels of matrix metalloproteinases in human atherosclerotic plaques and evaluation of radiolabeled inhibitors as imaging agents for plaque vulnerability
20. Correction to "Discovery and Structure-Based Design of Potent Covalent PPARγ Inverse-Agonists BAY-4931 and BAY-0069".
21. Studies toward the Development of New Silicon-Containing Building Blocks for the Direct 18F-Labeling of Peptides
22. Design, Synthesis, and Initial Evaluation of a High Affinity Positron Emission Tomography Probe for Imaging Matrix Metalloproteinases 2 and 9
23. 18F-Radiolabeling of Aromatic Compounds Using Triarylsulfonium Salts
24. Single-step radiofluorination of peptides using continuous flow microreactor
25. 18F-Labeled Bombesin Analog for Specific and Effective Targeting of Prostate Tumors Expressing Gastrin-Releasing Peptide Receptors
26. In Vitro and in Vivo Characterization of Novel 18F-Labeled Bombesin Analogues for Targeting GRPR-Positive Tumors
27. ChemInform Abstract: Nucleophilic Ring-Opening of Activated Aziridines: A One-Step Method for Labeling Biomolecules with Fluorine-18.
28. Direct One-Step18F-Labeling of Peptides via Nucleophilic Aromatic Substitution
29. Nucleophilic ring-opening of activated aziridines: A one-step method for labeling biomolecules with fluorine-18
30. Synthesis, 18F-Labeling, and in Vitro and in Vivo Studies of Bombesin Peptides Modified with Silicon-Based Building Blocks
31. Silicon-Based Building Blocks for One-Step18F-Radiolabeling of Peptides for PET Imaging
32. Siliciumbausteine für eine einstufige18F-Radiomarkierung von Peptiden für die PET-Bildgebung
33. Tandem Intramolecular Michael-Aldol Reaction as a Tool for the Construction of the C-Ring of Hexacyclinic Acid
34. Asymmetric Total Synthesis of Complex Marine Natural Products
35. Synthesis of the A,B,C‐Ring System of Hexacyclinic Acid.
36. Synthesis of the A,B,C-Ring System of Hexacyclinic Acid
37. Asymmetric Total Synthesis of Complex Marine Natural Products.
38. 18F-Radiolabeling of Aromatic Compounds Using Triarylsulfonium Salts.
39. 18F-Labeled Bombesin Analog for Specific and Effective Targeting of Prostate Tumors Expressing Gastrin-Releasing Peptide Receptors.
40. Discovery and Structure-Based Design of Potent Covalent PPARγ Inverse-Agonists BAY-4931and BAY-0069
41. Silicon-Based Building Blocks for One-Step 18F-Radiolabeling of Peptides for PET Imaging
42. Siliciumbausteine für eine einstufige 18F-Radiomarkierung von Peptiden für die PET-Bildgebung
43. Direct one-step 18F-labeling of peptides via nucleophilic aromatic substitution.
44. Silicon-based building blocks for one-step 18F-radiolabeling of peptides for PET imaging.
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