Search Results - "SAKANE; KAZUO" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

In Vitro Activities of a New Lipopeptide Antifungal Agent, FK463, against a Variety of Clinically Important Fungi

In Vitro Activities of a New Lipopeptide Antifungal Agent, FK463, against a Variety of Clinically Important Fungi

by TAWARA, S, IKEDA, F, KAWABATA, K, TAKASUGI, H, SAKANE, K, TANAKA, H, MATSUMOTO, F, KUWAHARA, S, MAKI, K, MORISHITA, Y, OTOMO, K, TERATANI, N, GOTO, T, TOMISHIMA, M, OHKI, H, YAMADA, A
Published in Antimicrobial Agents and Chemotherapy (01.01.2000)

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Design, Synthesis and Biological Evaluation of a Novel Series of Potent, Orally Active Adenosine A1 Receptor Antagonists with High Blood-Brain Barrier Permeability

Design, Synthesis and Biological Evaluation of a Novel Series of Potent, Orally Active Adenosine A1 Receptor Antagonists with High Blood-Brain Barrier Permeability

by KURODA, Satoru, TAKAMURA, Fujiko, TENDA, Yoshiyuki, ITANI, Hiromichi, TOMISHIMA, Yasuyo, AKAHANE, Atsushi, SAKANE, Kazuo
Published in Chemical & pharmaceutical bulletin (01.08.2001)

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Discovery of FR166124, a novel water-soluble pyrazolo-[1,5-a]pyridine adenosine A1 receptor antagonist

Discovery of FR166124, a novel water-soluble pyrazolo-[1,5-a]pyridine adenosine A1 receptor antagonist

by KURODA, S, AKAHANE, A, ITANI, H, NISHIMURA, S, DURKIN, K, KINOSHITA, T, TENDA, Y, SAKANE, K
Published in Bioorganic & medicinal chemistry letters (19.07.1999)

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New reagents for controlled release of nitric oxide. Structure-stability relationships

New reagents for controlled release of nitric oxide. Structure-stability relationships

by Kato, Masayuki, Nishino, Shigetaka, Ohno, Mitsuko, Fukuyama, Shinichi, Kita, Yasuhiro, Hirasawa, Yoshimi, Nakanishi, Isao, Takasugi, Hisashi, Sakane, Kazuo
Published in Bioorganic & medicinal chemistry letters (01.01.1996)

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Synthesis of the water-soluble adenosine A1 receptor antagonist FR166124 through a novel sequential Horner-Emmons / isomerization reaction

Synthesis of the water-soluble adenosine A1 receptor antagonist FR166124 through a novel sequential Horner-Emmons / isomerization reaction

by Kuroda, Satoru, Akahane, Atsushi, Itani, Hiromichi, Nishimura, Shintaro, Durkin, Kieran, Kinoshita, Takayoshi, Nakanishi, Isao, Sakane, Kazuo
Published in Tetrahedron (01.08.1999)

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Novel adenosine A 1 receptor antagonists. Synthesis and structure–activity relationships of a novel series of 3-(2-cyclohexenyl-3-oxo-2,3-dihydropyridazin-6-yl)-2-phenylpyrazolo[1,5- a ]pyridines

Novel adenosine A 1 receptor antagonists. Synthesis and structure–activity relationships of a novel series of 3-(2-cyclohexenyl-3-oxo-2,3-dihydropyridazin-6-yl)-2-phenylpyrazolo[1,5- a ]pyridines

by Kuroda, Satoru, Akahane, Atsushi, Itani, Hiromichi, Nishimura, Shintaro, Durkin, Kieran, Tenda, Yoshiyuki, Sakane, Kazuo
Published in Bioorganic & medicinal chemistry (01.01.2000)

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A Concise, Practical Synthesis of the Pyrido[3,2,1-i,j]Cinnoline Ring System of Potent DNA Gyrase Inhibitors

A Concise, Practical Synthesis of the Pyrido[3,2,1-i,j]Cinnoline Ring System of Potent DNA Gyrase Inhibitors

by Barrett, David, Sasaki, Hiroshi, Tsutsumi, Hideo, Murata, Masayoshi, Terasawa, Takeshi, Sakane, Kazuo
Published in Journal of organic chemistry (01.06.1995)

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A novel synthesis of the pyrazolo[1,5- a]quinoline ring system. New N1-C2 bridged DNA gyrase inhibitors via a novel tandem 1,4-conjugate addition-Michael [3+2] annulation process

A novel synthesis of the pyrazolo[1,5- a]quinoline ring system. New N1-C2 bridged DNA gyrase inhibitors via a novel tandem 1,4-conjugate addition-Michael [3+2] annulation process

by Barrett, David, Sasaki, Hiroshi, Kinoshita, Takayoshi, Fujikawa, Akihiko, Sakane, Kazuo
Published in Tetrahedron (01.06.1996)

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FR109615, A NEW ANTIFUNGAL ANTIBIOTIC FROM STREPTOMYCES SETONII: TAXONOMY, FERMENTATION, ISOLATION, PHYSICO-CHEMICAL PROPERTIES AND BIOLOGICAL ACTIVITY

FR109615, A NEW ANTIFUNGAL ANTIBIOTIC FROM STREPTOMYCES SETONII: TAXONOMY, FERMENTATION, ISOLATION, PHYSICO-CHEMICAL PROPERTIES AND BIOLOGICAL ACTIVITY

by IWAMOTO, TOSHIRO, TSUJII, EISAKU, EZAKI, MASAMI, FUJIE, AKIHIKO, HASHIMOTO, SEIJI, OKUHARA, MASAKUNI, KOHSAKA, MASANOBU, IMANAKA, HIROSHI, KAWABATA, KOHJI, INAMOTO, YOSHIKO, SAKANE, KAZUO
Published in Journal of antibiotics (1990)

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Alkylation of 1-[N-(Hydroxymethyl)-N-methylamino]-4-quinolones. An Improved Preparation of Intermediates for Novel Potent Tricyclic Quinolone Antibacterial Agents

Alkylation of 1-[N-(Hydroxymethyl)-N-methylamino]-4-quinolones. An Improved Preparation of Intermediates for Novel Potent Tricyclic Quinolone Antibacterial Agents

by Barrett, David, Sasaki, Hiroshi, Kinoshita, Takayoshi, Tsutsumi, Hideo, Sakane, Kazuo
Published in Bulletin of the Chemical Society of Japan (01.05.1996)

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SYNTHESIS AND STRUCTURE DETERMINATION OF FR109615, A NEW ANTIFUNGAL ANTIBIOTIC

SYNTHESIS AND STRUCTURE DETERMINATION OF FR109615, A NEW ANTIFUNGAL ANTIBIOTIC

by KAWABATA, KOHJI, INAMOTO, YOSHIKO, SAKANE, KAZUO, IWAMOTO, TOSHIRO, HASHIMOTO, SEIJI
Published in Journal of antibiotics (1990)

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Synthesis and Biological Properties of a Novel Cephalosporin FR86521 Having Potent Activity Against Methicillin-resistant Staphylococcus aureus (MRSA)

Synthesis and Biological Properties of a Novel Cephalosporin FR86521 Having Potent Activity Against Methicillin-resistant Staphylococcus aureus (MRSA)

by KISHI, KOHEI, OHKI, HIDENORI, OKUDA, SHINYA, KAWABATA, KOHJI, SAKANE, KAZUO, MATSUMOTO, YOSHIMI, MATSUMOTO, SATORU, TAWARA, SHUICHI
Published in Journal of antibiotics (1999)

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FK037, A NEW PARENTERAL CEPHALOSPORIN WITH A BROAD ANTIBACTERIAL SPECTRUM: SYNTHESIS AND ANTIBACTERIAL ACTIVITY

FK037, A NEW PARENTERAL CEPHALOSPORIN WITH A BROAD ANTIBACTERIAL SPECTRUM: SYNTHESIS AND ANTIBACTERIAL ACTIVITY

by OHKI, HIDENORI, KAWABATA, KOHJI, OKUDA, SHINYA, KAMIMURA, TOSHIAKI, SAKANE, KAZUO
Published in Journal of antibiotics (1993)

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Studies on 3'-Quaternary Ammonium Cephalosporins II. Synthesis and Antibacterial Activity of 7.BETA.-((Z)-2-(2-Aminothiazol-4-yl)-2- methoxyiminoacetamido)cephalosporin Derivatives Bearing Various Quaternary Ammonium Methyl Groups at the 3 Position

Studies on 3'-Quaternary Ammonium Cephalosporins II. Synthesis and Antibacterial Activity of 7.BETA.-((Z)-2-(2-Aminothiazol-4-yl)-2- methoxyiminoacetamido)cephalosporin Derivatives Bearing Various Quaternary Ammonium Methyl Groups at the 3 Position

by OHKI, HIDENORI, KAWABATA, KOHJI, OKUDA, SHINYA, KAMIMURA, TOSHIAKI, SAKANE, KAZUO
Published in Journal of antibiotics (1995)

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Studies on β-Lactam Antibiotics: Synthesis and Antibacterial Activity of Novel C-3 Alkyne-substituted Cephalosporins

Studies on β-Lactam Antibiotics: Synthesis and Antibacterial Activity of Novel C-3 Alkyne-substituted Cephalosporins

by BARRETT, DAVID, TERASAWA, TAKESHI, OKUDA, SHINYA, KAWABATA, KOHJI, YASUDA, NOBUYOSHI, KAMIMURA, TOSHIAKI, SAKANE, KAZUO, TAKAYA, TAKAO
Published in Journal of antibiotics (01.01.1997)

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Epimerization Induced by a Remote Cationic Center in Potent New Carbapenems

Epimerization Induced by a Remote Cationic Center in Potent New Carbapenems

by AZAMI, Hidenori, BARRETT, David, CHIBA, Toshiyuki, FUJIKAWA, Akihiko, SAKANE, Kazuo, SHIRAI, Fumiyuki
Published in Chemical & pharmaceutical bulletin (01.01.1997)

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REVISED STRUCTURE AND THE CHEMICAL TRANSFORMATIONS OF FR900148

REVISED STRUCTURE AND THE CHEMICAL TRANSFORMATIONS OF FR900148

by YASUDA, NOBUYOSHI, SAKANE, KAZUO
Published in Journal of antibiotics (1991)

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Synthesis and antifungal activity of FR 109615 analogs

Synthesis and antifungal activity of FR 109615 analogs

by OHKI, HIDENORI, INAMOTO, YOSHIKO, KAWABATA, KOHJI, KAMIMURA, TOSHIAKI, SAKANE, KAZUO
Published in Journal of antibiotics (1991)

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Synthesis and antibacterial activity of 7.BETA.-(1-(2-aminothiazol-4-yl)-1-cyclopropanecarboxyamido)cephem derivatives

Synthesis and antibacterial activity of 7.BETA.-(1-(2-aminothiazol-4-yl)-1-cyclopropanecarboxyamido)cephem derivatives

by NISHIMURA, SHINTARO, YASUDA, NOBUYOSHI, SASAKI, HIROSHI, SAKANE, KAZUO, TAKAYA, TAKAO
Published in Journal of antibiotics (1990)

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STUDIES ON β-LACTAM ANTIBIOTICS: XIX. STRUCTURE-ACTIVITY RELATIONSHIPS OF CEPHALOSPORINS HAVING A THIADIAZOLYLTHIOMETHYL GROUP AT THE C-3 SIDE CHAIN

STUDIES ON β-LACTAM ANTIBIOTICS: XIX. STRUCTURE-ACTIVITY RELATIONSHIPS OF CEPHALOSPORINS HAVING A THIADIAZOLYLTHIOMETHYL GROUP AT THE C-3 SIDE CHAIN

by INAMOTO, YOSHIKO, GOTO, JIRO, SAKANE, KAZUO, KAMIMURA, TOSHIAKI, TAKAYA, TAKAO
Published in Journal of antibiotics (1991)

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