β-Cyanoalanine Production by Marine Bacteria on Cyanide-Free Medium and Its Specific Inhibitory Activity toward Cyanobacteria von YOSHIKAWA, K, ADACHI, K, NISHIJIMA, M, TAKADERA, T, TAMAKI, S, HARADA, K.-I, MOCHIDA, K, SANO, H

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Inhibitor Studies of a New Antibiotic, Korormicin, 2-n-Heptyl-4-hydroxyquinoline N-oxide and Ag+ toward the Na+-Translocating NADH-Quinone Reductase from the Marine Vibrio alginoly... von NAKAYAMA, Yuji, HAYASHI, Maki, YOSHIKAWA, Kazuhiro, MOCHIDA, Kenichi, UNEMOTO, Tsutomu

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Planar Structure and Antibacterial Activity of Korormicin Derivatives Isolated from Pseudoalteromonas sp. F-420 von YOSHIKAWA, KAZUHIRO, ADACHI, KYOKO, NISHIDA, FUMIKO, MOCHIDA, KENICHI

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The absolute configuration and total synthesis of korormicin von Uehara, Hisatoshi, Oishi, Tohru, Yoshikawa, Kazuhiro, Mochida, Kenichi, Hirama, Masahiro

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Korormicin, an Antibiotic Specific for Gram-negative Marine Bacteria, Strongly Inhibits the Respiratory Chain-linked Na+-Translocating NADH: Quinone Reductase from the Marine Vibri... von YOSHIKAWA, KAZUHIRO, NAKAYAMA, YUJI, HAYASHI, MAKI, UNEMOTO, TSUTOMU, MOCHIDA, KENICHI

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Convenient preparation of chiral ethylenediamine linked to d-glucose von Mikata, Yuji, Yoneda, Kazumi, Tanase, Tomoaki, Kinoshita, Isamu, Doe, Matsumi, Nishida, Fumiko, Mochida, Kenichi, Yano, Shigenobu

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General Synthesis of Useful Chelating Reagents Having a Sugar Unit, 1,3-Diamino-2-propyl β-D-Glucopyranoside and 1,3-Diamino-2-propyl α-D-Mannopyranoside von Yano, Shigenobu, Shinohara, Yoshie, Mogami, Kaoru, Yokoyama, Mika, Tanase, Tomoaki, Sakakibara, Toru, Nishida, Fumiko, Mochida, Kenichi, Kinoshita, Isamu, Doe, Matsumi, Ichihara, Kanako, Naruta, Yoshinori, Mehrkhodavandi, Parisa, Buglyó, Péter, Song, Bin, Orvig, Chris, Mikata, Yuji

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NADPH Regeneration by Glucose Dehydrogenase from Gluconobacter scleroides for l-Leucovorin Synthesis von Eguchi, Tamotsu, Kuge, Yukihiro, Inoue, Kunimi, Yoshikawa, Naohiro, Mochida, Kenichi, Uwajima, Takayuki

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IN VITRO AND IN VIVO ANTIBACTERIAL ACTIVITY OF KT3777, A NEW ORALLY ACTIVE CARBACEPHEM von SATO, KIYOSHI, OKACHI, RYO, MATSUKUMA, IKUO, MOCHIDA, KENICHI, HIRATA, TADASHI

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Production of Dihydrofolate Reductase by Cloned Escherichia coli and Its Application to Asymmetric Synthesis of l-Leucovorin von Ohshiro, Takashi, Kuge, Yukihiro, Igarashi, Akiko, Mochida, Kenichi, Iwakura, Masanori, Uwajima, Takayuki

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Synthetic studies on 1-carbacephem antibiotics: new synthetic approach to 3H-carbacephems von MOCHIDA, K, HIRATA, T

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Isoprenoid quinones in an aerobic hyperthermophilic archaeon, Aeropyrum pernix von NISHIDA, F, NISHIJIMA, M, MOCHIDA, K, SANO, H, NOMURA, N, SAKO, Y, MARUYAMA, T

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SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF NOVEL 3-SUBSTITUTED CARBACEPHEMS von MOCHIDA, KENICHI, OGASA, TAKEHIRO, SHIMADA, JUNICHI, HIRATA, TADASHI, SATO, KIYOSHI, OKACHI, RYO

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Synthesis and Biological Evaluation of 3-Chloro-1-carbacephem Compounds von MATSUKUMA, Ikuo, YOSHIYE, Shigeo, MOCHIDA, Kenichi, HASHIMOTO, Yukio, SATO, Kiyoshi, OKACHI, Ryo, HIRATA, Tadashi

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AMINOTHIAZOLYLGLYCYL DERIVATIVES OF CARBACEPHEM ANTIBIOTICS: II. SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF NOVEL AMINOTHIAZOLYL CEPHEM COMPOUNDS WITH HYDROXYPYRIDONE MOIETY von MOCHIDA, KENICHI, ONO, YASUYUKI, YAMASAKI, MOTOO, SHIRAKI, CHIHIRO, HIRATA, TADASHI, SATO, KIYOSHI, OKACHI, RYO

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AMINOTHIAZOLYLGLYCYL DERIVATIVES OF CARBACEPHEMS: I. SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF NOVEL CARBACEPHEMS WITH SUBSTITUTED AMINOTHIAZOLYL GROUPS von MOCHIDA, KENICHI, SHIRAKI, CHIHIRO, YAMASAKI, MOTOO, HIRATA, TADASHI, SATO, KIYOSHI, OKACHI, RYO

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Isoprenoid quinones in an aerobic hyperthermophilic archaeon, Aeropyrum pernix von Nishida, Fumiko, Nishijima, Miyuki, Mochida, Kenichi, Sano, Hiroshi, Nomura, Norimichi, Sako, Yoshihiko, Maruyama, Tadashi

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Isoprenoid quinones in an aerobic hyperthermophilic archaeon, Aeropyrum pernix von Nishida, Fumiko, Nishijima, Miyuki, Mochida, Kenichi, Sano, Hiroshi, Nomura, Norimichi, Sako, Yoshihiko, Maruyama, Tadashi

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Microbial hydroxylation of 2-phenylpropionic acid von KUGE, Yukihiro, MOCHIDA, Kenichi, UWAJIMA, Takayuki

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CHEMICAL MODIFICATION OF FORTIMICINS: II. SELECTIVE PROTECTION OF FORTIMICINS A AND B von SATO, MORIYUKI, MOCHIDA, KENICHI, MORI, YASUKI, SHIRAHATA, KUNIKATSU

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