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20. Aryl bis-sulfonamides bind to the active site of a homotrimeric isoprenoid biosynthesis enzyme IspF and extract the essential divalent metal cation cofactor

21. Structure of GTP cyclohydrolase I from Listeria monocytogenes, a potential anti‐infective drug target.

22. IspH-Protein aus Escherichia coli und IspDF-Protein aus Campylobacter jejuni

23. Prodrugs of Reverse Fosmidomycin Analogues

26. Binding Modes of Reverse Fosmidomycin Analogs toward the Antimalarial Target IspC

27. IspC as Target for Antiinfective Drug Discovery: Synthesis, Enantiomeric Separation, and Structural Biology of Fosmidomycin Thia Isosters

29. IspH-Protein aus Escherichia coli und IspDF-Protein aus Campylobacter jejuni

31. Reverse Fosmidomycin Derivatives against the Antimalarial Drug Target IspC (Dxr)

34. Synthesis and Antiplasmodial Activity of Highly Active Reverse Analogues of the Antimalarial Drug Candidate Fosmidomycin

35. Thiazolopyrimidine Inhibitors of 2‐Methylerythritol 2,4‐Cyclodiphosphate Synthase (IspF) from Mycobacterium tuberculosis and Plasmodium falciparum

40. IspH Protein of Escherichia coli: Studies on Iron−Sulfur Cluster Implementation and Catalysis

42. Biosynthesis of isoprenoids

45. Probing the reaction mechanism of lspH protein by x-ray structure analysis.

47. IspH Protein of Escherichia coil: Studies on Iron--Sulfur Cluster Implementation and Catalysis.

49. Aryl bis-sulfonamides bind to the active site of a homotrimeric isoprenoid biosynthesis enzyme IspF and extract the essential divalent metal cation cofactor

50. Aryl bis-sulfonamides bind to the active site of a homotrimeric isoprenoid biosynthesis enzyme IspF and extract the essential divalent metal cation cofactor

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