Drug intelligence / Profile preview

4-Borono-2-18F-fluoro-L-phenylalanine-fructose

Development stage
Unknown
Lead developer
The University of Tennessee Medical Center
Modality
Beta Emitters → Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Small Molecules, Alpha Emitters → Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

4-Borono-2-(\^{18})F-fluoro-L-phenylalanine-fructose (commonly referred to as 18F-BPA-Fr or 18F-FBPA) is a radiolabeled amino acid analog used primarily as a positron emission tomography (PET) imaging agent. It is an analog of boronophenylalanine (BPA), which is used in boron neutron capture therapy (BNCT), an experimental form of radiotherapy for cancers such as glioblastoma multiforme and melanoma. The primary purpose of administering 18F-BPA-Fr is to noninvasively assess the biodistribution and tumor uptake of BPA prior to BNCT, enabling patient selection and treatment planning. Mechanistically, it enters tumor cells mainly via L-type amino acid transporters, reflecting the pharmacokinetics and tissue distribution expected from therapeutic BPA administration[1][2][3][5]. The compound is metabolically stable, with its tumoral accumulation correlating with DNA synthesis activity[1]. PET imaging with this tracer allows estimation of boron concentration in tumors before BNCT[3][7].

Other names
fluorine-18-BPA-fructosefluorine18-BPA-fructosefluorine 18-BPA-fructose[18F]fluoro-boronophenylalanine-fructose
02

Targets

SLC superfamily (Solute carrier superfamily)

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