Trifluoroacetyl-HYNIC peptides: synthesis and 99mTc radiolabeling.

J Med Chem

Cancer Research Group, Department of Biosciences, University of Kent, Canterbury, Kent CT2 7NJ, United Kingdom.

Published: March 2007

Fmoc-lys(HYNIC-Boc)-OH, a precursor for solid-phase synthesis of 99mTc-labeled peptides, was synthesized efficiently without HPLC purification. HPLC-ESMS showed that deprotection and decoupling of peptide from the resin with trifluoroacetic acid gave initially HYNIC-peptide, which was trifluoroacetylated upon prolonged incubation. The trifluoroacetyl-HYNIC group was hydrolyzed during 99mTc labeling, rendering deprotection unnecessary. Trifluoroacetyl-HYNIC peptide was 99mTc-labeled as efficiently, producing the same product, as HYNIC-peptide. These modifications enhance the versatility of HYNIC for 99mTc peptide labeling.

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http://dx.doi.org/10.1021/jm061274lDOI Listing

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Similar Publications

Trifluoroacetyl-HYNIC peptides: synthesis and 99mTc radiolabeling.

J Med Chem

March 2007

Cancer Research Group, Department of Biosciences, University of Kent, Canterbury, Kent CT2 7NJ, United Kingdom.

Fmoc-lys(HYNIC-Boc)-OH, a precursor for solid-phase synthesis of 99mTc-labeled peptides, was synthesized efficiently without HPLC purification. HPLC-ESMS showed that deprotection and decoupling of peptide from the resin with trifluoroacetic acid gave initially HYNIC-peptide, which was trifluoroacetylated upon prolonged incubation. The trifluoroacetyl-HYNIC group was hydrolyzed during 99mTc labeling, rendering deprotection unnecessary.

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