Tumor uptake of radiolabelled pyrimidine bases and pyrimidine nucleosides in animal models: VI. 1-(3′-[36Cl]-chloro-, 1-(3′-[82Br]-bromo- and 1-(3′-[123I]-iodo-3′-deoxy-β-D-arabinofuranosyl)uracil
Author:
Publisher
Elsevier BV
Subject
Radiology, Nuclear Medicine and imaging,Nuclear Energy and Engineering,Radiation
Reference19 articles.
1. Synthesis of 21-[82Br]-21-deoxyuridine
2. Tumor uptake of radiolabeled pyrimidine bases and pyrimidine nucleosides in animal models —III. 2′-[82Br]-Bromo-2′-deoxyuridine
3. Tumour uptake of radiolabelled pyrimidine bases and pyrimidine nucleosides in animal models—IV. 2′-123I-iodo-2′-deoxyuridine
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1. Syntheses and Uses of Isotopically Labelled Organic Halides;PATAI'S Chemistry of Functional Groups;2009-12-15
2. Use of 5-[76Br]bromo-2'-fluoro-2'-deoxyuridine as a ligand for tumour proliferation: validation in an animal tumour model;European Journal of Nuclear Medicine and Molecular Imaging;2002-01
3. Elimination of nonspecific radioactivity from [76Br]bromide in PET study with [76Br]bromodeoxyuridine;Nuclear Medicine and Biology;1999-10
4. Tumour uptake of radiolabelled pyrimidine bases and pyrimidine nucleosides in animal models IX. Radiolabelled 1-(2′-fluoro-2′-deoxy-β-D-ribofuranosyl)uracil and 1-(2′-chloro-2′-deoxy-β-D-ribofuranosyl) uracil;The British Journal of Radiology;1986-03
5. Radiopharmaceuticals labelled with bromine isotopes;International Journal of Radiation Applications and Instrumentation. Part A. Applied Radiation and Isotopes;1986-01
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