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3]octreotide had a 6-fold better binding affinity than the uncomplexed ligand (complexed = 0.5 nM; uncomplexed = 3.0 nM): de Jong, M. Presentation at European Society of Nuclear Medicine Meeting, Barcelona, Spain, 1999. Abstract: de Jong, M.; Breeman, W. A. P.; Bernard, B. F.; van Gameren, A.; Schaar, M.; Bakker, W. H.; van der Pluijm, M. E.; Visser, T. J.; Maecke, H. R.; and Krenning, E. P. Tumor Uptake of the Radiolabeled Somatostatin Analog [DOTA-0, TYR-3]Octreotide is Dependent on the Peptide Amount. Eur. J. Nucl. Med. 1999, 26, abstract book 1026.
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3]octreotide had a 6-fold better binding affinity than the uncomplexed ligand (complexed = 0.5 nM; uncomplexed = 3.0 nM): de Jong, M. Presentation at European Society of Nuclear Medicine Meeting, Barcelona, Spain, 1999. Abstract: de Jong, M.; Breeman, W. A. P.; Bernard, B. F.; van Gameren, A.; Schaar, M.; Bakker, W. H.; van der Pluijm, M. E.; Visser, T. J.; Maecke, H. R.; and Krenning, E. P. Tumor Uptake of the Radiolabeled Somatostatin Analog [DOTA-0, TYR-3]Octreotide is Dependent on the Peptide Amount. Eur. J. Nucl. Med. 1999, 26, abstract book 1026.
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3]octreotate: Reubi, J. C.; Schaer, J.-C.; Waser, B.; Wenger, S.; Heppeler, A.; Schmitt, J. S.; Maecke, H. R. Affinity Profiles for Human Somatostatin Receptor Subtypes SST1-SST5 of Somatostatin Radiotracers Selected for Scintigraphic and Radiotherapeutic Use. Eur. J. Nucl. Med. 2000, 27, 273-282.
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3]-octreotide vs AR42J tumor membranes = 2.44 and 2.37 nM, respectively: Heppeler, A.; Froidevaux, S.; Eberle, A. N.; Maecke, H. R. Receptor Targeting for Tumor Localization and Therapy with Radiopeptides. Curr. Med. Chem. 2000, 7, 971-994.
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3]-octreotide vs AR42J tumor membranes = 2.44 and 2.37 nM, respectively: Heppeler, A.; Froidevaux, S.; Eberle, A. N.; Maecke, H. R. Receptor Targeting for Tumor Localization and Therapy with Radiopeptides. Curr. Med. Chem. 2000, 7, 971-994.
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Binding affinities for DOTA-AMBA and Lu-complexed peptide vs PC-3 cells = 4.75 and 2.50 nM, respectively: Lantry, L. E.; Cappelletti, E.; Maddalena, M. E.; Fox, J. S.; Feng, W.; Chen, J.; Thomas, R.; Eaton, S. M.; Bogdan, N. J.; Arunachalam, T.; Reubi, J. C.; Raju, N.; Metcalfe, E. C.; Lattuada, L.; Linder, K. E.; Swensen, R. E.; Tweedle, M. F.; Nunn, A. D. 177Lu-AMBA: Synthesis and Characterization of a Selective 177Lu-Labeled GRP-R Agonist for Systemic Radiotherapy of Prostate Cancer. J. Nucl. Med. 2006, 47, 1144-1147.
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Binding affinities for DOTA-AMBA and Lu-complexed peptide vs PC-3 cells = 4.75 and 2.50 nM, respectively: Lantry, L. E.; Cappelletti, E.; Maddalena, M. E.; Fox, J. S.; Feng, W.; Chen, J.; Thomas, R.; Eaton, S. M.; Bogdan, N. J.; Arunachalam, T.; Reubi, J. C.; Raju, N.; Metcalfe, E. C.; Lattuada, L.; Linder, K. E.; Swensen, R. E.; Tweedle, M. F.; Nunn, A. D. 177Lu-AMBA: Synthesis and Characterization of a Selective 177Lu-Labeled GRP-R Agonist for Systemic Radiotherapy of Prostate Cancer. J. Nucl. Med. 2006, 47, 1144-1147.
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