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Merck
  • Solid phase synthesis of [18F]labelled peptides for positron emission tomography.

Solid phase synthesis of [18F]labelled peptides for positron emission tomography.

Bioorganic & medicinal chemistry letters (2000-07-29)
J L Sutcliffe-Goulden, M J O'Doherty, S S Bansal
摘要

A strategy for the solid phase synthesis of [18F]labelled peptides has been developed. The peptides were prepared on solid support and acylated with 4-[18F]fluorobenzoic acid using HATU within 3 min and the labelled peptide was released from the solid support within 7 min. The [18F]labelled peptides were produced in good purity with a specific activity of 20-25 GBq/micromol.

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Sigma-Aldrich
对氟苯甲酸, 98%
Sigma-Aldrich
对氟苯甲酸, 99%, purified by sublimation