Search Results - "Schweiger, Lutz F."
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Fluorinase-Coupled Base Swaps: Synthesis of [¹⁸F]-5'-Deoxy-5'-fluorouridines
Published in Angewandte Chemie (International ed.) (01-01-2008)“…Making F‐ases: One‐pot fluorination/base‐swap biotransformations were developed by coupling the fluorinase enzyme to nucleoside phosphorylases to generate…”
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An enzymatic route to 5-deoxy-5-[18F]fluoro-D-ribose, a [18F]-fluorinated sugar for PET imaging
Published in Chemical communications (Cambridge, England) (01-01-2010)“…An efficient two-step, one-pot, biotransformation involving the fluorinase enzyme is described for the synthesis of 5-deoxy-5-[(18)F]fluororibose, a novel…”
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3
Synthesis, Radiosynthesis, and in vitro Studies on Novel Hypoxia PET Tracers Incorporating [18F]FDR
Published in European journal of organic chemistry (05-03-2021)“…We report the synthesis of five radiotracers incorporating different oxyamine spacers between the hypoxia‐reactive 2‐nitroimidazole moiety and the…”
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Last-Step Enzymatic [18F]-Fluorination of Cysteine-Tethered RGD Peptides Using Modified Barbas Linkers
Published in Chemistry : a European journal (25-07-2016)“…We report a last‐step fluorinase‐catalyzed [18F]‐fluorination of a cysteine‐containing RGD peptide. The peptide was attached through sulfur to a modified and…”
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[18F]-5-Fluoro-5-deoxyribose, an efficient peptide bioconjugation ligand for positron emission tomography (PET) imaging
Published in Chemical communications (Cambridge, England) (28-05-2012)“…[(18)F]-5-Fluoro-5-deoxyribose ([(18)F]-FDR) conjugates much more rapidly than [(18)F]-FDG under mild reaction conditions to peptides and offers new prospects…”
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Efficient bioconjugation of 5-fluoro-5-deoxy-ribose (FDR) to RGD peptides for positron emission tomography (PET) imaging of α(v)β(3) integrin receptor
Published in Organic & biomolecular chemistry (21-07-2013)“…The utility of 5-fluoro-5-deoxyribose (FDR) as an efficient bioconjugation agent for radiolabelling of the RGD peptides c(RGDfK) and c(RGDfC) is demonstrated…”
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Tumour imaging by Positron Emission Tomography using fluorinase generated 5-[18 F]fluoro-5-deoxyribose as a novel tracer
Published in Nuclear medicine and biology (01-05-2013)“…Abstract Introduction 5-[18 F]Fluoro-5-deoxyribose ([18 F]FDR) 3 was prepared as a novel monosaccharide radiotracer in a two-step synthesis using the…”
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Fully-automated radiosynthesis and in vitro uptake investigation of [N-methyl-¹¹C]methylene blue
Published in Anticancer research (01-10-2013)“…Malignant melanoma is a type of skin cancer which can spread rapidly if not detected early and left untreated. Positron Emission Tomography (PET) is a powerful…”
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Decreased [18 F]fluoro-2-deoxy- d -glucose incorporation and increased glucose transport are associated with resistance to 5FU in MCF7 cells in vitro
Published in Nuclear medicine and biology (01-11-2007)“…Abstract Introduction Tumor refractoriness to chemotherapy is frequently due to the acquisition of resistance. Resistant cells selected by exposure to…”
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18F-barbiturates are PET tracers with diagnostic potential in Alzheimer's disease
Published in Chemical communications (Cambridge, England) (28-01-2013)“…Three fluoro-barbiturates were synthesised, showing in vivo sedative efficacy. One of them, [(18)F], was synthesised in radiofluorinated form. PET/CT Imaging…”
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Fluorinase‐Coupled Base Swaps: Synthesis of [18F]‐5′‐Deoxy‐5′‐fluorouridines
Published in Angewandte Chemie (15-12-2008)“…Fluorierung und Basentausch zur Herstellung von 5′‐Desoxy‐5′‐fluornucleosiden (FDAs) lassen sich in einem Eintopfprozess ausführen, wenn man das Enzym…”
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Fluorinase‐Coupled Base Swaps: Synthesis of [ 18 F]‐5′‐Deoxy‐5′‐fluorouridines
Published in Angewandte Chemie (15-12-2008)Get full text
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