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de Bruin, B., Kuhnast, B., Hinnen, F., Yaouancq, L., Amessou, M., Johannes, L., et al. (2005) 1-[3-(2-[F-18]fluoropyridin-3-yloxy)propyl]pyrrole-2,5-dione: Design, Synthesis, and Radiosynthesis of a New [F-18]fluoropyridine-based Maleimide Reagent for the Labeling of Peptides and Proteins. Bioconjugate Chemistry, 16, 406-420.
http://dx.doi.org/10.1021/bc0497463
has been cited by the following article:
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TITLE:
Fluorine-18 Radiochemistry: A Novel Thiol-Reactive Prosthetic Group, [18F]FBAMPy
AUTHORS:
Thomas M. Moore, Murthy R. Akula, George W. Kabalka
KEYWORDS:
Radiochemistry, Prosthetic Group, PET, Fluorine-18
JOURNAL NAME:
Natural Science,
Vol.8 No.1,
January
27,
2016
ABSTRACT: A novel thiol-reactive bifunctional agent, an analogue of fluorobenzaldehyde-O-[6-(2,5-dioxo-2,5- dihydro-pyrrol-1-yl)-hexyl]oxime, (FBAM) has been synthesized. The new prosthetic group, [18F]- FBAMPy, replaces the 4-fluorophenyl moiety with a 2-fluoropyridinyl moiety leading to increased polarity (FBAM analytical HPLC Rf = 6.4 min; FBAMPy Rf = 4.8 min) while retaining the sulfur-reactive pendant. By altering the polarity of the molecule, this new prosthetic group should have significant impact in coupling it with small peptides and other biomolecules.