๐”– Bobbio Scriptorium
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Session 7: Radionuclide Chemistry and Targetry


Publisher
John Wiley and Sons
Year
2003
Tongue
French
Weight
481 KB
Volume
46
Category
Article
ISSN
0022-2135

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๐Ÿ“œ SIMILAR VOLUMES


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๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 208 KB

## Introduction: The nuclide 225 Ac and its decay product 213 Bi have been identified as very suitable for targeted alpha-immuno-therapy [1]. First treatments of patients with acute myelogenous leukemia with a 213 Bi-labelled antibody HuM195 at Sloan Kettering Memorial Cancer Center, New York, pro

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## Aim In the recent years other -mostly metallic -radionuclides for PET gained more and more interest. However, for production of these alternative positron emitters the vast majority of them affords solid targets in form of metal foils, oxide or salt pellets [1, 2] which can not be operated by a

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The prenyl group is known as an important structural building block in natural and medicinal products. The isotopic substitution of one of the two methyl groups with a [ 11 C]methyl group would provide an access to a large number of interesting 11 C-labelled compounds. Here we report a strategy for

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Selenocysteine (Sec; U in one-letter code), the 21st amino acid existing in all selenoproteins, has unique biochemical properties due to its selenium atom, including a low pK a and a high reactivity with many electrophilic agents. Mammalian thioredoxin reductase (TrxR) is a selenoprotein with a redo