Discovery of E2730, a novel selective uncompetitive GAT1 inhibitor, as a candidate for anti‐seizure medication
Fukushima, Kazuyuki, Higashiyama, Hiroyuki, Kazuta, Yuji, Hashimoto, Keisuke, Watanabe, Naoto, Furuya, Yoshiaki, Ito, Yoshimasa, Wu, Ting, Kosasa, Takashi, Talos, Delia M., Song, Yeri, Roberts, Nicholas S., Jensen, Frances E., Hanada, Takahisa, Ido, Katsutoshi
Published in Epilepsia open (01.09.2023)
Published in Epilepsia open (01.09.2023)
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Journal Article
Cyclopropane-Based Conformational Restriction of Histamine. (1S,2S)-2-(2-Aminoethyl)-1-(1H-imidazol-4-yl)cyclopropane, a Highly Selective Agonist for the Histamine H3 Receptor, Having a cis-Cyclopropane Structure
Kazuta, Yuji, Hirano, Kazufumi, Natsume, Kentaro, Yamada, Shizuo, Kimura, Ryohei, Matsumoto, Shun-ichiro, Furuichi, Kiyoshi, Matsuda, Akira, Shuto, Satoshi
Published in Journal of medicinal chemistry (08.05.2003)
Published in Journal of medicinal chemistry (08.05.2003)
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Journal Article
Construction of a cis-Cyclopropane via Reductive Radical Decarboxylation. Enantioselective Synthesis of cis- and trans-1-Arylpiperazyl-2-phenylcyclopropanes Designed as Antidopaminergic Agents
Yamaguchi, Kazuya, Kazuta, Yuji, Abe, Hiroshi, Matsuda, Akira, Shuto, Satoshi
Published in Journal of organic chemistry (28.11.2003)
Published in Journal of organic chemistry (28.11.2003)
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Journal Article
Synthesis of derivatives of (1 S,2 R)-1-phenyl-2-[( S)-1-aminopropyl] -N,N-diethylcyclopropanecarboxamide (PPDC) modified at the 1-aromatic moiety as novel NMDA receptor antagonists: the aromatic group is essential for the activity
Kazuta, Yuji, Tsujita, Ryuichi, Yamashita, Kanako, Uchino, Shigeo, Kohsaka, Shinichi, Matsuda, Akira, Shuto, Satoshi
Published in Bioorganic & medicinal chemistry (01.12.2002)
Published in Bioorganic & medicinal chemistry (01.12.2002)
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Journal Article
Conformational Analysis of the NMDA Receptor Antagonist (1S,2R)-1-Phenyl-2-[(S)-1-aminopropyl]-N,N-diethylcyclopropanecarboxamide (PPDC) Designed by a Novel Conformational Restriction Method Based on the Structural Feature of Cyclopropane Ring
Ono, Sizuka, Ogawa, Kiyoshi, Yamashita, Kanako, Yamamoto, Tamotsu, Kazuta, Yuji, Matsuda, Akira, Shuto, Satoshi
Published in Chemical & pharmaceutical bulletin (01.07.2002)
Published in Chemical & pharmaceutical bulletin (01.07.2002)
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Journal Article
Silinanyl Rhodamines and Silinanyl Fluoresceins for Super-Resolution Microscopy
Hara, Daiki, Uno, Shin-nosuke, Motoki, Takafumi, Kazuta, Yuji, Norimine, Yoshihiko, Suganuma, Masatoshi, Fujiyama, Shingo, Shimaoka, Yuki, Yamashita, Kazuto, Okada, Masaya, Nishikawa, Youichi, Amino, Hiroyuki, Iwanaga, Shigeki
Published in The journal of physical chemistry. B (12.08.2021)
Published in The journal of physical chemistry. B (12.08.2021)
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Journal Article
Design, synthesis, and structure–activity relationships of a series of novel N-aryl-2-phenylcyclopropanecarboxamide that are potent and orally active orexin receptor antagonists
Yoshida, Yu, Terauchi, Taro, Naoe, Yoshimitsu, Kazuta, Yuji, Ozaki, Fumihiro, Beuckmann, Carsten T., Nakagawa, Makoto, Suzuki, Michiyuki, Kushida, Ikuo, Takenaka, Osamu, Ueno, Takashi, Yonaga, Masahiro
Published in Bioorganic & medicinal chemistry (01.11.2014)
Published in Bioorganic & medicinal chemistry (01.11.2014)
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Journal Article
Stereochemical Diversity-Oriented Conformational Restriction Strategy. Development of Potent Histamine H3 and/or H4 Receptor Antagonists with an Imidazolylcyclopropane Structure
Watanabe, Mizuki, Kazuta, Yuji, Hayashi, Hideki, Yamada, Shizuo, Matsuda, Akira, Shuto, Satoshi
Published in Journal of medicinal chemistry (07.09.2006)
Published in Journal of medicinal chemistry (07.09.2006)
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Journal Article
Stereochemical diversity-oriented conformational restriction strategy. Development of potent histamine H-3 and/or H-4 receptor antagonists with an imidazolylcyclopropane structure
Watanabe, Mizuki, Kazuta, Yuji, Hayashi, Hideki, Yamada, Shizuo, Matsuda, Akira, Shuto, Satoshi
Published in Journal of medicinal chemistry (07.09.2006)
Published in Journal of medicinal chemistry (07.09.2006)
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Journal Article
Corrigendum to “Design, synthesis, and structure–activity relationships of a series of novel N-aryl-2-phenylcyclopropanecarboxamide that are potent and orally active orexin receptor antagonists” [Bioorg. Med. Chem. 22 (2014) 6071–6088]
Yoshida, Yu, Terauchi, Taro, Naoe, Yoshimitsu, Kazuta, Yuji, Ozaki, Fumihiro, Beuckmann, Carsten T., Nakagawa, Makoto, Suzuki, Michiyuki, Kushida, Ikuo, Takenaka, Osamu, Ueno, Takashi, Yonaga, Masahiro
Published in Bioorganic & medicinal chemistry (01.07.2015)
Published in Bioorganic & medicinal chemistry (01.07.2015)
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Journal Article
Synthesis of (1S,2R)-1-phenyl-2-[(S)-1-aminoalkyl]-N,N-diethylcyclopropanecarboxamides as novel NMDA receptor antagonists having a unique NMDA receptor subtype selectivity
Kazuta, Y, Tsujita, R, Uchino, S, Kamiyama, N, Mochizuki, D, Yamashita, K, Ohmori, Y, Yamashita, A, Yamamoto, T, Kohsaka, S, Matsuda, A, Shuto, S
Published in Perkin 1 : an international journal of organic and bio-organic chemistry (26.04.2002)
Published in Perkin 1 : an international journal of organic and bio-organic chemistry (26.04.2002)
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Journal Article
Synthesis of 1-arylpiperazyl-2-phenylcyclopropanes designed as antidopaminergic agents: Cyclopropane-based conformationally restricted analogs of haloperidol
Yamaguchi, Kazuya, Kazuta, Yuji, Hirano, Kazufumi, Yamada, Shizuo, Matsuda, Akira, Shuto, Satoshi
Published in Bioorganic & medicinal chemistry (01.10.2008)
Published in Bioorganic & medicinal chemistry (01.10.2008)
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Journal Article
Cyclopropane-based conformational restriction of histamine. (1S,2S)-2-(2-aminoethyl)-1-(1H-imidazol-4-yl)cyclopropane, a highly selective agonist for the histamine H-3 receptor, having a cis-cyclopropane structure
Kazuta, Y, Hirano, K, Natsume, K, Yamada, S, Kimura, R, Matsumoto, SI, Furuichi, K, Matsuda, A, Shuto, S
Published in Journal of medicinal chemistry (08.05.2003)
Published in Journal of medicinal chemistry (08.05.2003)
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Journal Article
A Systematic Study of the Hydride Reduction of Cyclopropyl Ketones with Structurally Simplified Substrates. Highly Stereoselective Reductions of Trans-Substituted Cyclopropyl Ketones via the Bisected s-Cis Conformation
Kazuta, Yuji, Abe, Hiroshi, Yamamoto, Tamotsu, Matsuda, Akira, Shuto, Satoshi
Published in Journal of organic chemistry (02.05.2003)
Published in Journal of organic chemistry (02.05.2003)
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Journal Article
Highly Stereoselective Grignard Addition to Cis-Substituted C-Cyclopropylaldonitrones. The Bisected s-Trans Transition State Can Be Stabilized Effectively by the Lewis Acid-Coordination
Kazuta, Yuji, Abe, Hiroshi, Matsuda, Akira, Shuto, Satoshi
Published in Journal of organic chemistry (24.12.2004)
Published in Journal of organic chemistry (24.12.2004)
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Journal Article
The unusual 1,4-chelation-controlled nucleophilic addition to aldehydes with high stereoselectivity. A systematic study of stereoselectivity in the addition reaction of carbon nucleophiles to cis-substituted cyclopropanecarbaldehydes
Kazuta, Yuji, Abe, Hiroshi, Yamamoto, Tamotsu, Matsuda, Akira, Shuto, Satoshi
Published in Tetrahedron (26.07.2004)
Published in Tetrahedron (26.07.2004)
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