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64Cu-CB-TE2A-Y3-TATE

 
National Institutes of Health

Papers overview

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2013
2013
N-mono/dimethylated TE2A tetraazamacrocycles (MM-TE2A and DM-TE2A) were synthesized in high yields. Both Cu-MM/DM-TE2A complexes… Expand
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2012
2012
Somatostatin receptors (SSTr) are overexpressed in a wide range of neuroendocrine tumors, making them excellent targets for… Expand
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2012
2012
Ethylene cross-bridged cyclam with two acetate pendant arms, ECB-TE2A, is known to form the most kinetically stable (64)Cu… Expand
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2012
2012
OBJECTIVES Radiolabeled somatostatin analogs have become important agents for molecular imaging and targeted radiotherapy of… Expand
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2010
2010
PurposeThe development of a new bifunctional chelator, which holds radiometals strongly in living systems, is a prerequisite for… Expand
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Highly Cited
2008
Highly Cited
2008
Recently, the somatostatin receptor subtype 2 (SSTR2) selective antagonist sst2-ANT was determined to have a high affinity for… Expand
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2007
2007
64Cu radiopharmaceuticals have shown tumor growth inhibition in tumor-bearing animal models with a relatively low radiation dose… Expand
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2005
2005
The cross-bridged tetraamine ligand 4,11-bis(carboxymethyl)-1,4,8,11-tetraazabicyclo[6.6.2]hexadecane (H2CB-TE2A) allows… Expand
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Highly Cited
2004
Highly Cited
2004
Purpose: Somatostatin receptors (SSTr) are expressed on many neuroendocrine tumors, and several radiotracers have been developed… Expand
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