Search Results - "NAMBA, Eiko"

Muraminomicins, novel ester derivatives: in vitro and in vivo antistaphylococcal activity by Kagoshima, Yoshiko, Tokumitsu, Akane, Masuda, Takeshi, Namba, Eiko, Inoue, Harumi, Sugihara, Chika, Yokoyama, Mizuka, Yamamoto, Yuko, Suzuki, Keiko, Iida, Kouki, Tamura, Akihiro, Fujita, Yoko, Takatsu, Toshio, Konosu, Toshiyuki, Koga, Tetsufumi

“…Novel muraminomicin derivatives with antimicrobial activity against methicillin-resistant Staphylococcus aureus (MRSA) were synthesized by esterification of…”
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Potent In Vitro Activity of Tomopenem (CS-023) against Methicillin-Resistant Staphylococcus aureus and Pseudomonas aeruginosa by KOGA, Tetsufumi, MASUDA, Nobuhisa, KAKUTA, Masayo, NAMBA, Eiko, SUGIHARA, Chika, FUKUOKA, Takashi

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In Vivo Pharmacodynamic Activity of Tomopenem (formerly CS-023) against Pseudomonas aeruginosa and Methicillin-Resistant Staphylococcus aureus in a Murine Thigh Infection Model by SUGIHARA, Kiyoshi, SUGIHARA, Chika, KOGA, Tetsufumi, MATSUSHITA, Yoko, YAMAMURA, Naotoshi, UEMORI, Mitsutoshi, TOKUMITSU, Akane, INOUE, Harumi, KAKUTA, Masayo, NAMBA, Eiko, NASU, Hatsumi

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Affinity of Tomopenem (CS-023) for Penicillin-Binding Proteins in Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa by KOGA, Tetsufumi, SUGIHARA, Chika, KAKUTA, Masayo, MASUDA, Nobuhisa, NAMBA, Eiko, FUKUOKA, Takashi

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Synthesis and SAR of 1,3-thiazolyl thiophene and pyridine derivatives as potent, orally active and S1P3-sparing S1P1 agonists by Asano, Masayoshi, Nakamura, Tsuyoshi, Sekiguchi, Yukiko, Mizuno, Yumiko, Yamaguchi, Takahiro, Tamaki, Kazuhiko, Shimozato, Takaichi, Doi-Komuro, Hiromi, Kagari, Takashi, Tomisato, Wataru, Inoue, Ryotaku, Yuita, Hiroshi, Oguchi-Oshima, Keiko, Kaneko, Reina, Nara, Futoshi, Kawase, Yumi, Masubuchi, Noriko, Nakayama, Shintaro, Koga, Tetsufumi, Namba, Eiko, Nasu, Hatsumi, Nishi, Takahide

“…A series of 1,3-thiazole derivatives were synthesized as potent, orally bioavailable S1P3-sparing S1P1 agonists. One of them, 24c, exhibited favorable efficacy…”
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Antimicrobial and rapid bactericidal activities of sitafloxacin and other agents against Streptococcus pyogenes by Namba, Eiko, Okumura, Ryo, Chiba, Megumi, Hoshino, Kazuki, Tateda, Kazuhiro

“…We evaluated the in vitro activity of sitafloxacin against Japanese clinical isolates of Streptococcus pyogenes by broth microdilution susceptibility testing…”
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In Vitro and In Vivo Activities of DS-2969b, a Novel GyrB Inhibitor, and Its Water-Soluble Prodrug, DS11960558, against Methicillin-Resistant Staphylococcus aureus by Barman, Tarani Kanta, Kumar, Manoj, Mathur, Tarun, Namba, Eiko, Singh, Diksha, Chaira, Tridib, Kurosaka, Yuichi, Yamada, Makiko, Upadhyay, Dilip Jatashankar, Masuda, Nobuhisa

“…DS-2969b is a novel GyrB inhibitor under clinical development. In this study, the activity of DS-2969b and the activities of DS-2969b and its water-soluble…”
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Discovery of a compound which acts as a bacterial UMP kinase PyrH inhibitor by Yoshida, Tatsuhiko, Nasu, Hatsumi, Namba, Eiko, Ubukata, Osamu, Yamashita, Makoto

“…Abstract PyrH is a member of the UMP kinase family that catalyses the conversion of UMP to UDP, an essential step in the pyrimidine metabolic pathway in a…”
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Discovery of a compound that acts as a bacterial PyrG (CTP synthase) inhibitor by YOSHIDA, Tatsuhiko, NASU, Hatsumi, NAMBA, Eiko, UBUKATA, Osamu, YAMASHITA, Makoto

“…PyrG (CTP synthase) catalyses the conversion of UTP to CTP, an essential step in the pyrimidine metabolic pathway in a variety of bacteria, including those…”
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Absorption, elimination, and metabolism of CS-1036, a novel α-amylase inhibitor in rats and monkeys, and the relationship between gastrointestinal distribution and suppression of glucose absorption by Honda, Tomohiro, Kaneno-Urasaki, Yoko, Murai, Takahiro, Kakuta, Masayo, Nasu, Hatsumi, Namba, Eiko, Koga, Tetsufumi, Okuno, Akira, Izumi, Takashi

“…The absorption, metabolism, and excretion of (2R,3R,4R)-4-hydroxy-2-(hydroxymethyl)pyrrolidin-3-yl 4-O-(6-deoxy-β-d-glucopyranosyl)-α-d-glucopyranoside…”
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