Search Results - "FUMIYOSHI MATSUURA" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

A landmark in drug discovery based on complex natural product synthesis

A landmark in drug discovery based on complex natural product synthesis

by Kawano, Satoshi, Ito, Ken, Yahata, Kenzo, Kira, Kazunobu, Abe, Takanori, Akagi, Tsuyoshi, Asano, Makoto, Iso, Kentaro, Sato, Yuki, Matsuura, Fumiyoshi, Ohashi, Isao, Matsumoto, Yasunobu, Isomura, Minetaka, Sasaki, Takeo, Fukuyama, Takashi, Miyashita, Yusuke, Kaburagi, Yosuke, Yokoi, Akira, Asano, Osamu, Owa, Takashi, Kishi, Yoshito
Published in Scientific reports (17.06.2019)

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Total Synthesis and Stereochemistry of Pinnatoxins B and C

Total Synthesis and Stereochemistry of Pinnatoxins B and C

by Matsuura, Fumiyoshi, Hao, Junliang, Reents, Reinhard, Kishi, Yoshito
Published in Organic letters (20.07.2006)

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Stereochemistry of Pteriatoxins A, B, and C

Stereochemistry of Pteriatoxins A, B, and C

by Hao, Junliang, Matsuura, Fumiyoshi, Kishi, Yoshito, Kita, Masaki, Uemura, Daisuke, Asai, Naoki, Iwashita, Takashi
Published in Journal of the American Chemical Society (21.06.2006)

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Antidiabetic and Hypolipidemic Effects of a Novel Dual Peroxisome Proliferator-Activated Receptor (PPAR) α/γ Agonist, E3030, in db/db Mice and Beagle Dogs

Antidiabetic and Hypolipidemic Effects of a Novel Dual Peroxisome Proliferator-Activated Receptor (PPAR) α/γ Agonist, E3030, in db/db Mice and Beagle Dogs

by Kasai, Shunji, Inoue, Takashi, Yoshitomi, Hideki, Hihara, Taro, Matsuura, Fumiyoshi, Harada, Hitoshi, Shinoda, Masanobu, Tanaka, Isao
Published in Journal of Pharmacological Sciences (2008)

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O3H-4-4 Finding of selective tissue factor/factor VIIa complex inhibitor as a novel anticoagulant with lower bleeding risk

O3H-4-4 Finding of selective tissue factor/factor VIIa complex inhibitor as a novel anticoagulant with lower bleeding risk

by Nagakura Tadashi, Kimiyo Tabata, Kazunobu Kira, Shinsuke Hirota, Clark Richard, Fumiyoshi Matsuura, Hironobu Hisyohi
Published in Journal of Pharmacological Sciences (15.02.2014)

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Antidiabetic and Hypolipidemic Effects of a Novel Dual Peroxisome Proliferator-Activated Receptor (PPAR) a/γ Agonist, E3030, in db/db Mice and Beagle Dogs

Antidiabetic and Hypolipidemic Effects of a Novel Dual Peroxisome Proliferator-Activated Receptor (PPAR) a/γ Agonist, E3030, in db/db Mice and Beagle Dogs

by Shunji Kasai, Takashi Inoue, Hideki Yoshitomi, Taro Hihara, Fumiyoshi Matsuura, Hitoshi Harada, Masanobu Shinoda, Isao Tanaka
Published in Journal of Pharmacological Sciences (2008)

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Ten-Gram-Scale Total Synthesis of the Anticancer Drug Candidate E7130 to Supply Clinical Trials

Ten-Gram-Scale Total Synthesis of the Anticancer Drug Candidate E7130 to Supply Clinical Trials

by Kaburagi, Yosuke, Kira, Kazunobu, Yahata, Kenzo, Iso, Kentaro, Sato, Yuki, Matsuura, Fumiyoshi, Ohashi, Isao, Matsumoto, Yasunobu, Isomura, Minetaka, Sasaki, Takeo, Fukuyama, Takashi, Miyashita, Yusuke, Azuma, Hiroshi, Iida, Daisuke, Ishida, Tasuku, Itano, Wataru, Matsuda, Masaaki, Matsukura, Masayuki, Murai, Norio, Nagao, Satoshi, Seki, Masashi, Yamamoto, Akihiko, Yamamoto, Yuji, Yoneda, Naoki, Watanabe, Yuzo, Kamada, Atsushi, Kayano, Akio, Tagami, Katsuya, Asano, Osamu, Owa, Takashi, Kishi, Yoshito
Published in Organic letters (12.04.2024)

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What Does It Take to Develop Structurally Complex Molecules by Total Synthesis? Rapid Process Development and GMP Manufacturing of E7130 Drug Substance for First-in-Human Clinical Study

What Does It Take to Develop Structurally Complex Molecules by Total Synthesis? Rapid Process Development and GMP Manufacturing of E7130 Drug Substance for First-in-Human Clinical Study

by Sasaki, Takeo, Yahata, Kenzo, Isomura, Minetaka, Ohashi, Isao, Fukuyama, Takashi, Miyashita, Yusuke, Watanabe, Yuzo, Murai, Norio, Matsuda, Masaaki, Kamada, Atsushi, Kaburagi, Yosuke, Kira, Kazunobu, Iso, Kentaro, Sato, Yuki, Matsuura, Fumiyoshi, Matsumoto, Yasunobu, Azuma, Hiroshi, Iida, Daisuke, Ishida, Tasuku, Itano, Wataru, Nagao, Satoshi, Seki, Masashi, Yamamoto, Akihiko, Yamamoto, Yuji, Yoneda, Naoki, Matsukura, Masayuki, Asano, Osamu, Kayano, Akio, Tagami, Katsuya, Owa, Takashi, Kishi, Yoshito
Published in Organic process research & development (21.06.2024)

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Total synthesis of 2′-deoxymugineic acid and nicotianamine

Total synthesis of 2′-deoxymugineic acid and nicotianamine

by Matsuura, Fumiyoshi, Hamada, Yasumasa, Shioiri, Takayuki
Published in Tetrahedron (1994)

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Total synthesis of mugineic acid. Efficient use of the phenyl group as the carboxyl synthon

Total synthesis of mugineic acid. Efficient use of the phenyl group as the carboxyl synthon

by Matsuura, Fumiyoshi, Hamada, Yasumasa, Shioiri, Takayuki
Published in Tetrahedron (03.09.1993)

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Total Syntheses of Phytosiderophores, 3-Epi-Hydroxymugineic Acid, Distichonic Acid A, and 2′-Hydroxynicotianamine

Total Syntheses of Phytosiderophores, 3-Epi-Hydroxymugineic Acid, Distichonic Acid A, and 2′-Hydroxynicotianamine

by Matsuura, Fumiyoshi, Hamada, Yasumasa, Shioiri, Takayuki
Published in Tetrahedron (01.04.1994)

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Total synthesis of microginin, an angiotensin-converting enzyme inhibitory pentapeptide from the blue-green alga Microcystis aeruginosa

Total synthesis of microginin, an angiotensin-converting enzyme inhibitory pentapeptide from the blue-green alga Microcystis aeruginosa

by Matsuura, Fumiyoshi, Hamada, Yasumasa, Shioiri, Takayuki
Published in Tetrahedron (1994)

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Abstract 4183: Mechanism of action analysis of anti-CAF activity of E7130, a novel tumor-microenvironment ameliorator

Abstract 4183: Mechanism of action analysis of anti-CAF activity of E7130, a novel tumor-microenvironment ameliorator

by Abe, Takanori, Kawano, Satoshi, Ito, Ken, Yahata, Kenzo, Kira, Kazunobu, Akagi, Tsuyoshi, Asano, Makoto, Iso, Kentaro, Sato, Yuki, Matsuura, Fumiyoshi, Ohashi, Isao, Matsumoto, Yasunobu, Isomura, Minetaka, Sasaki, Takeo, Fukuyama, Takashi, Miyashita, Yusuke, Kaburagi, Yosuke, Yokoi, Akira, Asano, Osamu, Owa, Takashi, Kishi, Yoshito
Published in Cancer research (Chicago, Ill.) (15.08.2020)

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Abstract 4179: E7130 derived from total synthesis of halichondrin as a novel tumor-microenvironment ameliorator

Abstract 4179: E7130 derived from total synthesis of halichondrin as a novel tumor-microenvironment ameliorator

by Kawano, Satoshi, Abe, Takanori, Ito, Ken, Yahata, Kenzo, Kira, Kazunobu, Akagi, Tsuyoshi, Asano, Makoto, Iso, Kentaro, Sato, Yuki, Matsuura, Fumiyoshi, Ohashi, Isao, Matsumoto, Yasunobu, Isomura, Minetaka, Sasaki, Takeo, Fukuyama, Takashi, Miyashita, Yusuke, Kaburagi, Yosuke, Yokoi, Akira, Asano, Osamu, Owa, Takashi, Kishi, Yoshito
Published in Cancer research (Chicago, Ill.) (15.08.2020)

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E3024, 3-but-2-ynyl-5-methyl-2-piperazin-1-yl-3,5-dihydro-4H-imidazo [4,5-d]pyridazin-4-one tosylate, is a novel, selective and competitive dipeptidyl peptidase-IV inhibitor

E3024, 3-but-2-ynyl-5-methyl-2-piperazin-1-yl-3,5-dihydro-4H-imidazo [4,5-d]pyridazin-4-one tosylate, is a novel, selective and competitive dipeptidyl peptidase-IV inhibitor

by YASUDA, Nobuyuki, NAGAKURA, Tadashi, KIRA, Kazunobu, IKUTA, Hironori, OKADA, Toshimi, SAEKI, Takao, ASANO, Osamu, TANAKA, Isao, INOUE, Takashi, YAMAZAKI, Kazuto, KATSUTANI, Naruo, TAKENAKA, Osamu, CLARK, Richard, MATSUURA, Fumiyoshi, EMORI, Eita, YOSHIKAWA, Seiji
Published in European journal of pharmacology (01.10.2006)

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Selective tissue factor/factor VIIa Inhibitor, ER-410660, and its prodrug, E5539, have anti-venous and anti-arterial thrombotic effects with a low risk of bleeding

Selective tissue factor/factor VIIa Inhibitor, ER-410660, and its prodrug, E5539, have anti-venous and anti-arterial thrombotic effects with a low risk of bleeding

by Nagakura, Tadashi, Tabata, Kimiyo, Kira, Kazunobu, Hirota, Shinsuke, Clark, Richard, Matsuura, Fumiyoshi, Hiyoshi, Hironobu
Published in Thrombosis research (01.08.2013)

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EFFICIENT SYNTHESIS OF MUGINEIC ACID, A TYPICAL PHYTOSIDEROPHORE, UTILIZING THE PHENYL GROUP AS THE CARBOXYL SYNTHON

EFFICIENT SYNTHESIS OF MUGINEIC ACID, A TYPICAL PHYTOSIDEROPHORE, UTILIZING THE PHENYL GROUP AS THE CARBOXYL SYNTHON

by MATSUURA, F, HAMADA, Y, SHIOIRI, T
Published in Tetrahedron letters (01.12.1992)

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EFFICIENT SYNTHESIS OF PHYTOSIDEROPHORES, 3-EPI-HYDROXYMUGINEIC ACID AND DISTICHONIC ACID-A

EFFICIENT SYNTHESIS OF PHYTOSIDEROPHORES, 3-EPI-HYDROXYMUGINEIC ACID AND DISTICHONIC ACID-A

by MATSUURA, F, HAMADA, Y, SHIOIRI, T
Published in Tetrahedron letters (01.12.1992)

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A new efficient synthesis of nicotianamine and 2'-deoxymugineic acid

A new efficient synthesis of nicotianamine and 2'-deoxymugineic acid

by Shioiri, T, Irako, N, Sakakibara, S, Matsuura, F, Hamada, Y
Published in Heterocycles (01.01.1997)

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Unified Total Synthesis of Pteriatoxins and Their Diastereomers

Unified Total Synthesis of Pteriatoxins and Their Diastereomers

by Matsuura, Fumiyoshi, Peters, René, Anada, Masahiro, Harried, Scott S, Hao, Junliang, Kishi, Yoshito
Published in Journal of the American Chemical Society (14.06.2006)

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