Search Results - "YONAGA,MASAHIRO" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Discovery of (1R,2S)‑2-{[(2,4-Dimethylpyrimidin-5-yl)oxy]methyl}-2-(3-fluorophenyl)‑N‑(5-fluoropyridin-2-yl)cyclopropanecarboxamide (E2006): A Potent and Efficacious Oral Orexin Receptor Antagonist

Discovery of (1R,2S)‑2-{[(2,4-Dimethylpyrimidin-5-yl)oxy]methyl}-2-(3-fluorophenyl)‑N‑(5-fluoropyridin-2-yl)cyclopropanecarboxamide (E2006): A Potent and Efficacious Oral Orexin Receptor Antagonist

by Yoshida, Yu, Naoe, Yoshimitsu, Terauchi, Taro, Ozaki, Fumihiro, Doko, Takashi, Takemura, Ayumi, Tanaka, Toshiaki, Sorimachi, Keiichi, Beuckmann, Carsten T, Suzuki, Michiyuki, Ueno, Takashi, Ozaki, Shunsuke, Yonaga, Masahiro
Published in Journal of medicinal chemistry (11.06.2015)

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Enantioselective Total Synthesis of RQN-18690A (18-Deoxyherboxidiene)

Enantioselective Total Synthesis of RQN-18690A (18-Deoxyherboxidiene)

by Matsumoto, Yasunobu, Hibino, Kazuhiro, Yonaga, Masahiro, Kakeya, Hideaki, Hayashi, Yujiro
Published in Organic letters (15.07.2016)

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Synthesis and pharmacological profile of serofendic acids A and B

by Terauchi, Taro, Asai, Naoki, Doko, Takashi, Taguchi, Ryota, Takenaka, Osamu, Sakurai, Hideki, Yonaga, Masahiro, Kimura, Teiji, Kajiwara, Akiharu, Niidome, Tetsuhiro, Kume, Toshiaki, Akaike, Akinori, Sugimoto, Hachiro
Published in Bioorganic & medicinal chemistry (15.11.2007)

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Activation of γ-Secretase Trimming Activity by Topological Changes of Transmembrane Domain 1 of Presenilin 1

Activation of γ-Secretase Trimming Activity by Topological Changes of Transmembrane Domain 1 of Presenilin 1

by Cai, Tetsuo, Yonaga, Masahiro, Tomita, Taisuke
Published in The Journal of neuroscience (13.12.2017)

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Isolation of a Diterpenoid Substance with Potent Neuroprotective Activity from Fetal Calf Serum

Isolation of a Diterpenoid Substance with Potent Neuroprotective Activity from Fetal Calf Serum

by Kume, Toshiaki, Asai, Naoki, Nishikawa, Hiroyuki, Mano, Nariyasu, Terauchi, Taro, Taguchi, Ryota, Shirakawa, Hisashi, Osakada, Fumitaka, Mori, Hiroki, Asakawa, Naoki, Yonaga, Masahiro, Nishizawa, Yukio, Sugimoto, Hachiro, Shimohama, Shun, Katsuki, Hiroshi, Kaneko, Shuji, Akaike, Akinori
Published in Proceedings of the National Academy of Sciences - PNAS (05.03.2002)

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One-Pot Sequential 1,4-and 1,2-Reductions of alpha,beta-Unsaturated delta-Lactones to the Corresponding delta-Lactols with CuCl and NaBH4 in Methanol

One-Pot Sequential 1,4-and 1,2-Reductions of alpha,beta-Unsaturated delta-Lactones to the Corresponding delta-Lactols with CuCl and NaBH4 in Methanol

by Matsumoto, Yasunobu, Yonaga, Masahiro
Published in Synlett (22.07.2014)

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Practical Synthesis of Chiral Emopamil Left Hand as a Bioactive Motif

Practical Synthesis of Chiral Emopamil Left Hand as a Bioactive Motif

by Kimura, Teiji, Yamamoto, Noboru, Suzuki, Yuichi, Kawano, Koki, Norimine, Yoshihiko, Ito, Koichi, Nagato, Satoshi, Iimura, Yoichi, Yonaga, Masahiro
Published in Journal of organic chemistry (23.08.2002)

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Synthesis and absolute configuration of serofendic acids

Synthesis and absolute configuration of serofendic acids

by Terauchi, Taro, Asai, Naoki, Yonaga, Masahiro, Kume, Toshiaki, Akaike, Akinori, Sugimoto, Hachiro
Published in Tetrahedron letters (13.05.2002)

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Discovery of 2‑(2-Oxo-1-phenyl-5-pyridin-2-yl-1,2-dihydropyridin-3-yl)benzonitrile (Perampanel): A Novel, Noncompetitive α‑Amino-3-hydroxy-5-methyl-4-isoxazolepropanoic Acid (AMPA) Receptor Antagonist

Discovery of 2‑(2-Oxo-1-phenyl-5-pyridin-2-yl-1,2-dihydropyridin-3-yl)benzonitrile (Perampanel): A Novel, Noncompetitive α‑Amino-3-hydroxy-5-methyl-4-isoxazolepropanoic Acid (AMPA) Receptor Antagonist

by Hibi, Shigeki, Ueno, Koshi, Nagato, Satoshi, Kawano, Koki, Ito, Koichi, Norimine, Yoshihiko, Takenaka, Osamu, Hanada, Takahisa, Yonaga, Masahiro
Published in Journal of medicinal chemistry (13.12.2012)

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Palladium-Catalyzed Direct Hydroxymethylation of Aryl Halides and Inflates with Potassium Acetoxymethyltrifluoroborate

Palladium-Catalyzed Direct Hydroxymethylation of Aryl Halides and Inflates with Potassium Acetoxymethyltrifluoroborate

by Murai, Norio, Yonaga, Masahiro, Tanaka, Keigo
Published in Organic letters (02.03.2012)

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Palladium-Catalyzed Direct Hydroxymethylation of Aryl Halides and Triflates with Potassium Acetoxymethyltrifluoroborate

Palladium-Catalyzed Direct Hydroxymethylation of Aryl Halides and Triflates with Potassium Acetoxymethyltrifluoroborate

by Murai, Norio, Yonaga, Masahiro, Tanaka, Keigo
Published in Organic letters (02.03.2012)

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Synthesis of Optically Active Methyl 7.BETA.-Hydroxykaurenoate with Potent Neuroprotective Activity

Synthesis of Optically Active Methyl 7.BETA.-Hydroxykaurenoate with Potent Neuroprotective Activity

by Toyota, Masahiro, Matsuura, Kiminori, Yokota, Masahiro, Kimura, Manami, Yonaga, Masahiro, Sugimoto, Hachiro, Ihara, Masataka
Published in Chemical & pharmaceutical bulletin (2004)

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One-Pot Primary Aminomethylation of Aryl and Heteroaryl Halides with Sodium Phthalimidomethyltrifluoroborate

One-Pot Primary Aminomethylation of Aryl and Heteroaryl Halides with Sodium Phthalimidomethyltrifluoroborate

by Murai, Norio, Miyano, Masayuki, Yonaga, Masahiro, Tanaka, Keigo
Published in Organic letters (01.06.2012)

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Palladium-Catalyzed Direct Hydroxymethylation of Aryl Halides and Triflates with Potassium Acetoxymethyltrifluoroborate

Palladium-Catalyzed Direct Hydroxymethylation of Aryl Halides and Triflates with Potassium Acetoxymethyltrifluoroborate

by Murai, Norio, Yonaga, Masahiro, Tanaka, Keigo
Published in Organic letters (20.07.2012)

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Synthesis and Structure–Activity Relationships of Pyrazolo[1,5-a]pyridine Derivatives: Potent and Orally Active Antagonists of Corticotropin-Releasing Factor 1 Receptor

Synthesis and Structure–Activity Relationships of Pyrazolo[1,5-a]pyridine Derivatives: Potent and Orally Active Antagonists of Corticotropin-Releasing Factor 1 Receptor

by Takahashi, Yoshinori, Hibi, Shigeki, Hoshino, Yorihisa, Kikuchi, Koichi, Shin, Kogyoku, Murata-Tai, Kaoru, Fujisawa, Masae, Ino, Mitsuhiro, Shibata, Hisashi, Yonaga, Masahiro
Published in Journal of medicinal chemistry (14.06.2012)

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Design, synthesis, and structure–activity relationships of a series of novel N-aryl-2-phenylcyclopropanecarboxamide that are potent and orally active orexin receptor antagonists

Design, synthesis, and structure–activity relationships of a series of novel N-aryl-2-phenylcyclopropanecarboxamide that are potent and orally active orexin receptor antagonists

by 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)

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Dopamine D3 agonists disrupt social behavior in rats

Dopamine D3 agonists disrupt social behavior in rats

by KAGAYA, T.K, YONAGA, M, FURUYA, Y, HASHIMOTO, T, KUROKI, J, NISHIZAWA, Y
Published in Brain research (20.05.1996)

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Design, synthesis and structure–activity relationships of 5-alkylaminolquinolines as a novel series of CRF1 receptor antagonists

Design, synthesis and structure–activity relationships of 5-alkylaminolquinolines as a novel series of CRF1 receptor antagonists

by Takeda, Kunitoshi, Terauchi, Taro, Shin, Kogyoku, Ino, Mitsuhiro, Shibata, Hisashi, Yonaga, Masahiro
Published in Bioorganic & medicinal chemistry letters (15.07.2012)

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Design, synthesis, and structure–activity relationships of a series of 2-Ar-8-methyl-5-alkylaminoquinolines as novel CRF1 receptor antagonists

Design, synthesis, and structure–activity relationships of a series of 2-Ar-8-methyl-5-alkylaminoquinolines as novel CRF1 receptor antagonists

by Takeda, Kunitoshi, Terauchi, Taro, Hashizume, Minako, Shin, Kogyoku, Ino, Mitsuhiro, Shibata, Hisashi, Yonaga, Masahiro
Published in Bioorganic & medicinal chemistry letters (01.09.2012)

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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]

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]

by 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)

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