The Stereochemical Assignment and Conformational Analysis of the V/W-Ring Juncture of Maitotoxin von Cook, Laura R, Oinuma, Hitoshi, Semones, Marcus A, Kishi, Yoshito

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The neuroprotective action of JNK3 inhibitors based on the 6,7-dihydro-5H-pyrrolo[1,2-a]imidazole scaffold von GRACZYK, Piotr P, KHAN, Afzal, SMALES, Caroline, WHITFIELD, Jonathan, NEAME, Stephen J, SHAH, Bina, WILTON, Daniel, MORGAN, Louise, PATEL, Toshal, CHUNG, Raymond, DESMOND, Howard, STADDON, James M, BHATIA, Gurpreet S, SATO, Nobuaki, INOUE, Atsushi, PALMER, Vanessa, MEDLAND, Darren, NUMATA, Hirotoshi, OINUMA, Hitoshi, CATCHICK, Jacqueline, DUNNE, Angela, ELLIS, Moira

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Complete Relative Stereochemistry of Maitotoxin von Zheng, Wanjun, DeMattei, John A, Wu, Jiang-Ping, Duan, James J.-W, Cook, Laura R, Oinuma, Hitoshi, Kishi, Yoshito

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Synthesis and biological evaluation of substituted benzenesulfonamides as novel potent membrane-bound phospholipase A2 inhibitors von Oinuma, Hitoshi, Takamura, Tadanobu, Hasegawa, Takashi, Nomoto, Kenichi, Naitoh, Toshihiko, Daiku, Yoshiharu, Hamano, Sachiyuki, Kakisawa, Hiroshi, Minami, Norio

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The neuroprotective action of JNK3 inhibitors based on the 6,7-dihydro-5 H-pyrrolo[1,2- a]imidazole scaffold von Graczyk, Piotr P., Khan, Afzal, Bhatia, Gurpreet S., Palmer, Vanessa, Medland, Darren, Numata, Hirotoshi, Oinuma, Hitoshi, Catchick, Jacqueline, Dunne, Angela, Ellis, Moira, Smales, Caroline, Whitfield, Jonathan, Neame, Stephen J., Shah, Bina, Wilton, Daniel, Morgan, Louise, Patel, Toshal, Chung, Raymond, Desmond, Howard, Staddon, James M., Sato, Nobuaki, Inoue, Atsushi

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1H-indazole compound von OINUMA HITOSHI,OHI NORIHITO,SATO NOBUAKI

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4'-[(4-Piperidyl)carbonyl]methanesulfonanilides as potent, selective, bioavailable class III antiarrhythmic agents von Oinuma, Hitoshi, Miyake, Kazutoshi, Yamanaka, Motosuke, Nomoto, Kenichi, Katoh, Hiroshi, Sawada, Kohei, Shino, Mitsumasa, Hamano, Sachiyuki

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Novel 1H-indazole compound von OHI NORIHITO, OINUMA HITOSHI, SATO NOBUAKI

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1 von Oinuma, Hitoshi, Ohi, Norihito, Sato, Nobuaki, Soejima, Motohiro, Seshimo, Hidenori, Terauchi, Taro, Doko, Takashi, Kohmura, Naohiro

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1H-indazole compounds von SESHIMO HIDENORI, DOKO TAKASHI, SOEJIMA MOTOHIRO, KOHMURA NAOHIRO, OHI NORIHITO, TERAUCHI TARO, OINUMA HITOSHI, SATO NOBUAKI

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1H-INDAZOLVERBINDUNGEN DIE JNK HEMMEN von OHI, NORIHITO, SOEJIMA, MOTOHIRO, OINUMA, HITOSHI, SATO, NOBUAKI, KOHMURA, NAOHIRO, DOKO, TAKASHI, TERAUCHI, TARO, SESHIMO, HIDENORI

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1H-INDAZOLE COMPOUNDS INHIBITING JNK von OHI, NORIHITO, SOEJIMA, MOTOHIRO, OINUMA, HITOSHI, SATO, NOBUAKI, KOHMURA, NAOHIRO, DOKO, TAKASHI, TERAUCHI, TARO, SESHIMO, HIDENORI

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Novel 1H-indazole compounds von SESHIMO HIDENORI, DOKO TAKASHI, SOEJIMA MOTOHIRO, KOHMURA NAOHIRO, OHI NORIHITO, TERAUCHI TARO, OINUMA HITOSHI, SATO NOBUAKI

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Stereoselective syntheses of α-isosparteine von OINUMA, H, DAN, S, KAKISAWA, H

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1H-indazole compounds von Oinuma, Hitoshi, Ohi, Norihito, Sato, Nobuaki, Soejima, Motohiro, Seshimo, Hidenori, Terauchi, Taro, Doko, Takashi, Kohmura, Naohiro

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1H-indazole compounds von SESHIMO HIDENORI, DOKO TAKASHI, SOEJIMA MOTOHIRO, KOHMURA NAOHIRO, OHI NORIHITO, TERAUCHI TARO, OINUMA HITOSHI, SATO NOBUAKI

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Synthesis of antiarrhythmic [phenyl-14C]4′-[(4-piperidyl)carbonyl]-methanesulfonanilides von Oinuma, Hitoshi, Miyake, Kazutoshi, Yamanaka, Motosuke, Shino, Mitsumasa, Hamano, Sachiyuki

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Substd. thiazolo [3,2-a] azepine deriv von YONEDA NAOKI, SUDA SHINJI, OINUMA HITOSHI

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Jun kinase inhibitors von GRACZYK PIOTR, BHATIA GURPREET, PALMER VANESSA, MEDLAND DARREN PETER, OINUMA HITOSHI, KHAN AFZAL, NUMATA HIROTOSHI

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Jun kinase inhibitors von Graczyk, Piotr, Numata, Hirotoshi, Khan, Afzal, Palmer, Vanessa, Medland, Darren Peter, Oinuma, Hitoshi, Bhatia, Gurpreet

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