OpenURL Connection Search

Select item for more details and to access through your institution.

Synthesis and characterization of 11C‐labeled benzyl amidine derivatives as PET radioligands for GluN2B subunit of the NMDA receptors.
Published in:
Journal of Labelled Compounds & Radiopharmaceuticals, 2018, v. 61, n. 14, p. 1095, doi. 10.1002/jlcr.3691
By:
- Fuchigami, Takeshi;
- Fujimoto, Noriko;
- Haradahira, Terushi;
- Nojiri, Yumiko;
- Okauchi, Takashi;
- Maeda, Jun;
- Suhara, Tetsuya;
- Yamamoto, Fumihiko;
- Nakayama, Morio;
- Maeda, Minoru;
- Mukai, Takahiro
Publication type:
Article
Synthesis and preliminary PET study of the 5-HT7 receptor antagonist [11C]DR4446.
Published in:
Journal of Labelled Compounds & Radiopharmaceuticals, 2002, v. 45, n. 10, p. 857, doi. 10.1002/jlcr.606
By:
- Zhang, Ming-Rong;
- Haradahira, Terushi;
- Maeda, Jun;
- Okauchi, Takashi;
- Kida, Takayo;
- Obayashi, Shigeru;
- Suzuki, Kazutoshi;
- Suhara, Tetsuya
Publication type:
Article
Measurement of glycine binding site of N-methyl- d-asparate receptors in living human brain using 4-acetoxy derivative of L-703,717, 4-acetoxy-7-chloro-3-[3-(4-[11c] methoxybenzyl) phenyl]-2(1 H)-quinolone (AcL703) with positron emission tomography
Published in:
Synapse, 2007, v. 61, n. 10, p. 795, doi. 10.1002/syn.20415
By:
- Matsumoto, Ryohei;
- Haradahira, Terushi;
- Ito, Hiroshi;
- Fujimura, Yota;
- Seki, Chie;
- Ikoma, Yoko;
- Maeda, Jun;
- Arakawa, Ryosuke;
- Takano, Akihiro;
- Takahashi, Hidehiko;
- Higuchi, Makoto;
- Suzuki, Kazutoshi;
- Fukui, Kenji;
- Suhara, Tetsuya
Publication type:
Article
Effects of endogenous agonists, glycine and D-serine, on in vivo specific binding of [11C]L-703,717, a PET radioligand for the glycine-binding site of NMDA receptors.
Published in:
Synapse, 2003, v. 50, n. 2, p. 130, doi. 10.1002/syn.10254
By:
- Terushi Haradahira;
- Takashi Okauchi;
- Jun Maeda;
- Ming-Rong Zhang;
- Toru Nishikawa;
- Ryouichi Konno;
- Kazutoshi Suzuki
Publication type:
Article
A positron-emitter labeled glycineB site antagonist, [11C]L-703,717, preferentially binds to a cerebellar NMDA receptor subtype consisting of GluR ϵ3 subunit in vivo, but not in vitro.
Published in:
Synapse, 2002, v. 43, n. 2, p. 131, doi. 10.1002/syn.10029
By:
- Haradahira, Terushi;
- Okauchi, Takashi;
- Maeda, Jun;
- Zhang, Ming-Rong;
- Kida, Takayo;
- Kawabe, Kouichi;
- Mishina, Masayoshi;
- Watanabe, Yasuyoshi;
- Suzuki, Kazutoshi;
- Suhara, Tetsuya
Publication type:
Article
Synthesis and evaluation of 18F- and 11C-labelled 9,10-ethanobenzo[ b]quinolizinium derivatives for imaging of the NMDA receptor at the TCP-binding site.
Published in:
Journal of Labelled Compounds & Radiopharmaceuticals, 2000, v. 43, n. 4, p. 375, doi. 10.1002/(SICI)1099-1344(20000330)43:4<375::AID-JLCR324>3.0.CO;2-Q
By:
- Ishibashi, Nobuyasu;
- Kuwamura, Tsuneo;
- Sano, Hiromi;
- Yamamoto, Fumihiko;
- Haradahira, Terushi;
- Suzuki, Kazutoshi;
- Suhara, Tetsuya;
- Sasaki, Shigeki;
- Maeda, Minoru
Publication type:
Article
Synthesis and brain distribution of carbon-11 labeled analogs of antagonists for the NMDA receptor coupled PCP-binding site.
Published in:
Journal of Labelled Compounds & Radiopharmaceuticals, 1998, v. 41, n. 9, p. 843, doi. 10.1002/(SICI)1099-1344(1998090)41:9<843::AID-JLCR136>3.0.CO;2-H
By:
- Haradahira, Terushi;
- Sasaki, Sigeki;
- Maeda, Minoru;
- Kobayashi, Kaoru;
- Inoue, Osamu;
- Tomita, Urara;
- Nishikawa, Toru;
- Suzuki, Kazutoshi
Publication type:
Article
A new synthesis of 2-deoxy-2-[18f]fluoro-D-galactose using [18f]fluoride ion.
Published in:
Journal of Labelled Compounds & Radiopharmaceuticals, 1988, v. 25, n. 7, p. 721, doi. 10.1002/jlcr.2580250705
By:
- Haradahira, Terushi;
- Maeda, Minoru;
- Kai, Yasunobu;
- Kojima, Masaharu
Publication type:
Article
Alternative synthesis of no-carrier-added 2-deoxy-2-[18F]fluoro-D-glucose using [18F] fluoride ion.
Published in:
Journal of Labelled Compounds & Radiopharmaceuticals, 1988, v. 25, n. 5, p. 497, doi. 10.1002/jlcr.2580250504
By:
- Haradahira, Terushi;
- Maeda, Minoru;
- Kojima, Masaharu
Publication type:
Article
Tumor Visualization with a Radiodinated Phospholipid Ether.
Published in:
Journal of Nuclear Medicine, 1990, v. 31, n. 3, p. 332
By:
- Counsell, Raymond E.;
- Schwendner, Susan W.;
- Meyer, Karen L.;
- Haradahira, Terushi;
- Gross, Milton D.
Publication type:
Article

Found: 10

Synthesis and characterization of <sup>11</sup>C‐labeled benzyl amidine derivatives as PET radioligands for GluN2B subunit of the NMDA receptors.

Synthesis and preliminary PET study of the 5-HT<sub>7</sub> receptor antagonist [<sup>11</sup>C]DR4446.

Measurement of glycine binding site of N-methyl- d-asparate receptors in living human brain using 4-acetoxy derivative of L-703,717, 4-acetoxy-7-chloro-3-[3-(4-[<sup>11</sup>c] methoxybenzyl) phenyl]-2(1 H)-quinolone (AcL703) with positron emission tomography

Effects of endogenous agonists, glycine and D-serine, on in vivo specific binding of [<sup>11</sup>C]L-703,717, a PET radioligand for the glycine-binding site of NMDA receptors.

A positron-emitter labeled glycine<sub>B</sub> site antagonist, [<sup>11</sup>C]L-703,717, preferentially binds to a cerebellar NMDA receptor subtype consisting of GluR ϵ3 subunit in vivo, but not in vitro.

Synthesis and evaluation of <sup>18</sup>F- and <sup>11</sup>C-labelled 9,10-ethanobenzo[ b]quinolizinium derivatives for imaging of the NMDA receptor at the TCP-binding site.

Synthesis and brain distribution of carbon-11 labeled analogs of antagonists for the NMDA receptor coupled PCP-binding site.

A new synthesis of 2-deoxy-2-[<sup>18</sup>f]fluoro-D-galactose using [<sup>18</sup>f]fluoride ion.

Alternative synthesis of no-carrier-added 2-deoxy-2-[<sup>18</sup>F]fluoro-D-glucose using [<sup>18</sup>F] fluoride ion.

Tumor Visualization with a Radiodinated Phospholipid Ether.