Abstract
A new cross-bridged cyclam chelator, CB-TE1K1P, was developed for copper-based radiopharmaceuticals, and this chelator can be labelled with 64Cu under mild conditions in high specific activity. DBCO–PEG4–CB-TE1K1P was synthesized for conjugation to proteins, while Dde–CB-TE1K1P(tBu2)–OH was synthesized for solid-phase peptide synthesis. Examples of the conjugation chemistry, radiolabelling and serum stability of each are presented.
Original language | English (US) |
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Pages (from-to) | 43-45 |
Number of pages | 3 |
Journal | Chemical Communications |
Volume | 50 |
Issue number | 1 |
DOIs | |
State | Published - Nov 26 2014 |
Externally published | Yes |
ASJC Scopus subject areas
- Electronic, Optical and Magnetic Materials
- General Chemistry
- Ceramics and Composites
- Metals and Alloys
- Materials Chemistry
- Surfaces, Coatings and Films
- Catalysis