Cargando…
A high molar activity (18)F-labeled TAK-875 derivative for PET imaging of pancreatic β-cells
BACKGROUND: The free-fatty acid receptor-1 (FFA-1) is expressed by β-cells and is a promising target for molecular imaging of functional β-cell mass. Recently, the ((3-[(18)F]fluoropropyl)sulfonyl)propoxy-derivative of the high-affinity FFA-1 agonist TAK-875 ([(18)F]7) was reported. Here we describe...
Autores principales: | Dornan, Mark H., Petrenyov, Daniil, Simard, José-Mathieu, Aliaga, Antonio, Xiong, Guoming, Ghislain, Julien, Bedell, Barry, Poitout, Vincent, DaSilva, Jean N. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6301904/ http://dx.doi.org/10.1186/s41181-018-0051-2 |
Ejemplares similares
-
Synthesis of a (11)C-Isotopologue
of the B-Raf-Selective Inhibitor Encorafenib Using In-Loop
[(11)C]CO(2) Fixation
por: Dornan, Mark H., et al.
Publicado: (2020) -
A Novel Antidiabetic Drug, Fasiglifam/TAK-875, Acts as an Ago-Allosteric Modulator of FFAR1
por: Yabuki, Chiori, et al.
Publicado: (2013) -
Synthesis of the Novel AT(1) Receptor Tracer
[(18)F]Fluoropyridine–Candesartan via Click Chemistry
por: Abreu Diaz, Aida M., et al.
Publicado: (2020) -
Pharmacometric Approaches to Guide Dose Selection of the Novel GPR40 Agonist TAK-875 in Subjects With Type 2 Diabetes Mellitus
por: Naik, H, et al.
Publicado: (2013) -
Fasiglifam (TAK-875) Alters Bile Acid Homeostasis in Rats and Dogs: A Potential Cause of Drug Induced Liver Injury
por: Wolenski, Francis S., et al.
Publicado: (2017)