Search Results - "KOUJI HATTORI" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Discovery of Highly Potent and Selective Biphenylacylsulfonamide-Based β 3 -Adrenergic Receptor Agonists and Evaluation of Physical Properties as Potential Overactive Bladder Therapies: Part 5

Discovery of Highly Potent and Selective Biphenylacylsulfonamide-Based β 3 -Adrenergic Receptor Agonists and Evaluation of Physical Properties as Potential Overactive Bladder Therapies: Part 5

by Hattori, Kouji, Toda, Susumu, Imanishi, Masashi, Itou, Shinji, Nakajima, Yutaka, Washizuka, Kenichi, Araki, Takanobu, Hamashima, Hitoshi, Tomishima, Yasuyo, Sakurai, Minoru, Matsui, Shigeo, Imamura, Emiko, Ueshima, Koji, Yamamoto, Takao, Yamamoto, Nobuhiro, Ishikawa, Hirofumi, Nakano, Keiko, Unami, Naoko, Hamada, Kaori, Matsumura, Yasuhiro, Takamura, Fujiko
Published in Journal of medicinal chemistry (14.05.2009)

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Characteristics of a-Si films prepared by compressed magnetic field (CMF)-magnetron sputtering

Characteristics of a-Si films prepared by compressed magnetic field (CMF)-magnetron sputtering

by Hata, Tomonobu, Kamide, Yukihiro, Nakagawa, Shigeki, Hattori, Kouji
Published in Electronics & communications in Japan. Part 2, Electronics (1988)

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Discovery of a novel series of biphenyl benzoic acid derivatives as potent and selective human beta3-adrenergic receptor agonists with good oral bioavailability. Part I

Discovery of a novel series of biphenyl benzoic acid derivatives as potent and selective human beta3-adrenergic receptor agonists with good oral bioavailability. Part I

by Imanishi, Masashi, Tomishima, Yasuyo, Itou, Shinji, Hamashima, Hitoshi, Nakajima, Yutaka, Washizuka, Kenichi, Sakurai, Minoru, Matsui, Shigeo, Imamura, Emiko, Ueshima, Koji, Yamamoto, Takao, Yamamoto, Nobuhiro, Ishikawa, Hirofumi, Nakano, Keiko, Unami, Naoko, Hamada, Kaori, Matsumura, Yasuhiro, Takamura, Fujiko, Hattori, Kouji
Published in Journal of medicinal chemistry (27.03.2008)

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Discovery of a Novel Series of Biphenyl Benzoic Acid Derivatives as Potent and Selective Human β 3 -Adrenergic Receptor Agonists with Good Oral Bioavailability. Part I

Discovery of a Novel Series of Biphenyl Benzoic Acid Derivatives as Potent and Selective Human β 3 -Adrenergic Receptor Agonists with Good Oral Bioavailability. Part I

by Imanishi, Masashi, Tomishima, Yasuyo, Itou, Shinji, Hamashima, Hitoshi, Nakajima, Yutaka, Washizuka, Kenichi, Sakurai, Minoru, Matsui, Shigeo, Imamura, Emiko, Ueshima, Koji, Yamamoto, Takao, Yamamoto, Nobuhiro, Ishikawa, Hirofumi, Nakano, Keiko, Unami, Naoko, Hamada, Kaori, Matsumura, Yasuhiro, Takamura, Fujiko, Hattori, Kouji
Published in Journal of medicinal chemistry (01.03.2008)

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Discovery of novel series of benzoic acid derivatives containing biphenyl ether moiety as potent and selective human beta sub(3)-adrenergic receptor agonists: Part IV

Discovery of novel series of benzoic acid derivatives containing biphenyl ether moiety as potent and selective human beta sub(3)-adrenergic receptor agonists: Part IV

by Nakajima, Yutaka, Imanishi, Masashi, Itou, Shinji, Hamashima, Hitoshi, Tomishima, Yasuyo, Washizuka, Kenichi, Sakurai, Minoru, Matsui, Shigeo, Imamura, Emiko, Ueshima, Koji, Yamamoto, Takao, Yamamoto, Nobuhiro, Ishikawa, Hirofumi, Nakano, Keiko, Unami, Naoko, Hamada, Kaori, Hattori, Kouji
Published in Bioorganic & medicinal chemistry (01.09.2008)

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Discovery of a Novel Series of Biphenyl Benzoic Acid Derivatives as Highly Potent and Selective Human fi3 Adrenergic Receptor Agonists with Good Oral Bioavailability. Part II

Discovery of a Novel Series of Biphenyl Benzoic Acid Derivatives as Highly Potent and Selective Human fi3 Adrenergic Receptor Agonists with Good Oral Bioavailability. Part II

by IMANISHI, Masashi, ITOU, Shinji, UESHIMA, Koji, YAMAMOTO, Takao, YAMAMOTO, Nobuhiro, ISHIKAWA, Hirofumi, NAKANO, Keiko, UNAMI, Naoko, HAMADA, Kaori, MATSUMURA, Yasuhiro, TAKAMURA, Fujiko, HATTORI, Kouji, WASHIZUKA, Kenichi, HAMASHIMA, Hitoshi, NAKAJIMA, Yutaka, ARAKI, Takanobu, TOMISHIMA, Yasuyo, SAKURAI, Minoru, MATSUI, Shigeo, IMAMURA, Emiko
Published in Journal of medicinal chemistry (2008)

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Discovery of highly potent and selective biphenylacylsulfonamide-based beta sub(3)-adrenergic receptor agonists and molecular modeling based on the solved X-ray structure of the beta sub(2)-adrenergic receptor: Part 6

Discovery of highly potent and selective biphenylacylsulfonamide-based beta sub(3)-adrenergic receptor agonists and molecular modeling based on the solved X-ray structure of the beta sub(2)-adrenergic receptor: Part 6

by Hattori, Kouji, Orita, Masaya, Toda, Susumu, Imanishi, Masashi, Itou, Shinji, Nakajima, Yutaka, Tanabe, Daisuke, Washizuka, Kenichi, Araki, Takanobu, Sakurai, Minoru, Matsui, Shigeo, Imamura, Emiko, Ueshima, Koji, Yamamoto, Takao, Yamamoto, Nobuhiro, Ishikawa, Hirofumi, Nakano, Keiko, Unami, Naoko, Hamada, Kaori, Matsumura, Yasuhiro, Takamura, Fujiko
Published in Bioorganic & medicinal chemistry letters (01.08.2009)

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A simple stereoselective synthesis and biological evaluation of FR181157: Orally active prostacyclin mimetic

A simple stereoselective synthesis and biological evaluation of FR181157: Orally active prostacyclin mimetic

by HATTORI, Kouji, TABUCHI, Seiichiro, OKITSU, Osamu, TANIGUCHI, Kiyoshi
Published in Bioorganic & medicinal chemistry letters (15.12.2003)

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Discovery of diphenylcarbamate derivatives as highly potent and selective IP receptor agonists: Orally active prostacyclin mimetics. Part 3

Discovery of diphenylcarbamate derivatives as highly potent and selective IP receptor agonists: Orally active prostacyclin mimetics. Part 3

by Hattori, Kouji, Tanaka, Akira, Okitsu, Osamu, Tabuchi, Seiichiro, Taniguchi, Kiyoshi, Nishio, Mie, Koyama, Satoshi, Higaki, Masahide, Seki, Jiro, Sakane, Kazuo
Published in Bioorganic & medicinal chemistry letters (15.06.2005)

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Discovery of highly potent and selective biphenylacylsulfonamide-based β 3-adrenergic receptor agonists and molecular modeling based on the solved X-ray structure of the β 2-adrenergic receptor: Part 6

Discovery of highly potent and selective biphenylacylsulfonamide-based β 3-adrenergic receptor agonists and molecular modeling based on the solved X-ray structure of the β 2-adrenergic receptor: Part 6

by Hattori, Kouji, Orita, Masaya, Toda, Susumu, Imanishi, Masashi, Itou, Shinji, Nakajima, Yutaka, Tanabe, Daisuke, Washizuka, Kenichi, Araki, Takanobu, Sakurai, Minoru, Matsui, Shigeo, Imamura, Emiko, Ueshima, Koji, Yamamoto, Takao, Yamamoto, Nobuhiro, Ishikawa, Hirofumi, Nakano, Keiko, Unami, Naoko, Hamada, Kaori, Matsumura, Yasuhiro, Takamura, Fujiko
Published in Bioorganic & medicinal chemistry letters (2009)

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Practical preparation of α-hydroxy-β-amino ester units; Stereoselective synthesis of taxol side chain and norstatine

Practical preparation of α-hydroxy-β-amino ester units; Stereoselective synthesis of taxol side chain and norstatine

by Hattori, Kouji, Yamamoto, Hisashi
Published in Tetrahedron (28.02.1994)

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Discovery of novel series of benzoic acid derivatives containing biphenyl ether moiety as potent and selective human β 3-adrenergic receptor agonists: Part IV

Discovery of novel series of benzoic acid derivatives containing biphenyl ether moiety as potent and selective human β 3-adrenergic receptor agonists: Part IV

by Nakajima, Yutaka, Imanishi, Masashi, Itou, Shinji, Hamashima, Hitoshi, Tomishima, Yasuyo, Washizuka, Kenichi, Sakurai, Minoru, Matsui, Shigeo, Imamura, Emiko, Ueshima, Koji, Yamamoto, Takao, Yamamoto, Nobuhiro, Ishikawa, Hirofumi, Nakano, Keiko, Unami, Naoko, Hamada, Kaori, Hattori, Kouji
Published in Bioorganic & medicinal chemistry letters (2008)

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Neuroprotective effects of a novel poly(ADP-ribose) polymerase-1 inhibitor, 2-[3-[4-(4-chlorophenyl)-1-piperazinyl] propyl]-4(3H)-quinazolinone (FR255595), in an in vitro model of cell death and in mouse 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model of Parkinson's disease

Neuroprotective effects of a novel poly(ADP-ribose) polymerase-1 inhibitor, 2-[3-[4-(4-chlorophenyl)-1-piperazinyl] propyl]-4(3H)-quinazolinone (FR255595), in an in vitro model of cell death and in mouse 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model of Parkinson's disease

by Iwashita, Akinori, Yamazaki, Syunji, Mihara, Kayoko, Hattori, Kouji, Yamamoto, Hirofumi, Ishida, Junya, Matsuoka, Nobuya, Mutoh, Seitaro
Published in The Journal of pharmacology and experimental therapeutics (01.06.2004)

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Discovery of Diphenyloxazole and Nδ-Z-Ornithine Derivatives as Highly Potent and Selective Human Prostaglandin EP4 Receptor Antagonists

Discovery of Diphenyloxazole and Nδ-Z-Ornithine Derivatives as Highly Potent and Selective Human Prostaglandin EP4 Receptor Antagonists

by Hattori, Kouji, Tanaka, Akira, Fujii, Naoaki, Takasugi, Hisashi, Tenda, Yoshiyuki, Tomita, Masayuki, Nakazato, Shoko, Nakano, Keiko, Kato, Yasuko, Kono, Yutaka, Murai, Hidetsugu, Sakane, Kazuo
Published in Journal of medicinal chemistry (05.05.2005)

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A Case of Peritonitis Chronica Fibrosa Incapsulata Presenting as lleus after Irradiation

A Case of Peritonitis Chronica Fibrosa Incapsulata Presenting as lleus after Irradiation

by Sato, Atsushi, Kataoka, Makoto, Kuwabara, Yoshiyuki, Kureyama, Yasuyuki, Kawamura, Hiroyuki, Shinoda, Noriyuki, Kashima, Taketoshi, Hattori, Kouji, Sumida, Hidenori, Kimura, Masahiro, Nakano, Koichiro, Masaoka, Akira
Published in Nippon Shokaki Geka Gakkai zasshi (1994)

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Discovery of new diphenyloxazole derivatives containing a pyrrolidine ring: Orally active prostacyclin mimetics. Part 2

Discovery of new diphenyloxazole derivatives containing a pyrrolidine ring: Orally active prostacyclin mimetics. Part 2

by Hattori, Kouji, Okitsu, Osamu, Tabuchi, Seiichiro, Taniguchi, Kiyoshi, Nishio, Mie, Koyama, Satoshi, Seki, Jiro, Sakane, Kazuo
Published in Bioorganic & medicinal chemistry letters (01.07.2005)

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Discovery of diphenyloxazole and Ndelta-Z-ornithine derivatives as highly potent and selective human prostaglandin EP(4) receptor antagonists

Discovery of diphenyloxazole and Ndelta-Z-ornithine derivatives as highly potent and selective human prostaglandin EP(4) receptor antagonists

by Hattori, Kouji, Tanaka, Akira, Fujii, Naoaki, Takasugi, Hisashi, Tenda, Yoshiyuki, Tomita, Masayuki, Nakazato, Shoko, Nakano, Keiko, Kato, Yasuko, Kono, Yutaka, Murai, Hidetsugu, Sakane, Kazuo
Published in Journal of medicinal chemistry (05.05.2005)

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Discovery of Diphenyloxazole and Nδ-Z-Ornithine Derivatives as Highly Potent and Selective Human Prostaglandin EP 4 Receptor Antagonists

Discovery of Diphenyloxazole and Nδ-Z-Ornithine Derivatives as Highly Potent and Selective Human Prostaglandin EP 4 Receptor Antagonists

by Hattori, Kouji, Tanaka, Akira, Fujii, Naoaki, Takasugi, Hisashi, Tenda, Yoshiyuki, Tomita, Masayuki, Nakazato, Shoko, Nakano, Keiko, Kato, Yasuko, Kono, Yutaka, Murai, Hidetsugu, Sakane, Kazuo
Published in Journal of medicinal chemistry (01.05.2005)

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Characterization of a multidomain cellulase from an extremely thermophilic anaerobe strain NA10

Characterization of a multidomain cellulase from an extremely thermophilic anaerobe strain NA10

by Miyake, Katsuhide, Machida, Yuichi, Hattori, Kouji, Iijima, Shinji
Published in Journal of fermentation and bioengineering (01.01.1998)

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A Case of Early Synchronous Double Cancer of Esophagus and Stomach

A Case of Early Synchronous Double Cancer of Esophagus and Stomach

by Kawamura, Hiroyuki, Kataoka, Makoto, Kuwabara, Yoshiyuki, Kureyama, Yasuyuki, Iwata, Hiroshi, Shinoda, Noriyuki, Kashima, Taketoshi, Satou, Atsushi, Hattori, Kouji, Nakano, Kouichirou, Sumita, Hidenori, Masaoka, Akira
Published in Nippon Shokaki Geka Gakkai zasshi (1993)

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