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Nuclear Medicine and Biology|June 29, 2002
Synthesis, in vitro and in vivo pharmacology of a C-11 labeled analog of CP-101,606, (+/-)threo-1-(4-hydroxyphenyl)-2-[4-hydroxy-4-(p-[11C]methoxyphenyl)piperidino]-1-propanol, as a PET tracer for NR2B subunit-containing NMDA receptorsTerushi Haradahira, Jun Maeda, Takashi Okauchi, et al.Organic & Biomolecular Chemistry|August 20, 2024
Design and synthesis of an environment-sensitive 3-methyleneisoindolin-1-one fluorophore for labeling DNA-interacting proteinsMariko Aso, Chiyoe Ohta, Yixuan Liu, et al.Biochemistry|August 19, 2007
Extensive sugar modification improves triple helix forming oligonucleotide activity in vitro but reduces activity in vivoMd Rowshon Alam, Alokes Majumdar, Arun Kalliat Thazhathveetil, et al.Bioorganic & Medicinal Chemistry Letters|April 23, 2013
Identification of the fused bicyclic 4-amino-2-phenylpyrimidine derivatives as novel and potent PDE4 inhibitorsTaiji Goto, Akiko Shiina, Toshiharu Yoshino, et al.Bioorganic & Medicinal Chemistry|October 8, 2013
Synthesis and biological evaluation of 5-carbamoyl-2-phenylpyrimidine derivatives as novel and potent PDE4 inhibitorsTaiji Goto, Akiko Shiina, Toshiharu Yoshino, et al.Nuclear Medicine and Biology|March 4, 2008
Difference in brain distributions of carbon 11-labeled 4-hydroxy-2(1H)-quinolones as PET radioligands for the glycine-binding site of the NMDA ion channelTakeshi Fuchigami, Terushi Haradahira, Noriko Fujimoto, et al.Bioorganic & Medicinal Chemistry Letters|January 14, 2014
Identification of the 5,5-dioxo-7,8-dihydro-6H-thiopyrano[3,2-d]pyrimidine derivatives as highly selective PDE4B inhibitorsTaiji Goto, Akiko Shiina, Takeshi Murata, et al.Pageof 15