未登录Pharmacological profile of FK881(ASP6537), a novel potent and selective cyclooxygenase-1 inhibitor
Imanishi, Junko; Morita, Yoshiaki; Yoshimi, Eiji; Kuroda, Kanae; Masunaga, Tomoko; Yamagami, Kaoru; Kuno, Masako; Hamachi, Emi; Aoki, Satoshi; Takahashi, Fumie; Nakamura, Katsuya; Miyata, Susumu; Ohkubo, Yoshitaka; Mutoh, Seitaro
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收藏Prevention of progressive joint destruction in collagen-induced arthritis in rats by a novel matrix metalloproteinase inhibitor, FR255031
Ishikawa, T; Nishigaki, F; Miyata, S; Hirayama, Y; Minoura, K; Imanishi, J; Neya, M; Mizutani, T; Imamura, Y; Naritomi, Y; Murai, H; Ohkubo, Y; Kagayama, A; Mutoh, S
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收藏Efficacy of Oral Treatment With Tacrolimus in the Renal Transplant Model in Cynomolgus Monkeys
Kinugasa, Fumitaka; Nagatomi, Itsuo; Ishikawa, Hirofumi; Nakanishi, Tomonori; Maeda, Masashi; Hirose, Jun; Fukahori, Hidehiko; Ooshima, Shinsuke; Noto, Takahisa; Higashi, Yasuyuki; Seki, Nobuo; Mutoh, Seitaro
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收藏Mechanism by which a novel non-thiazolidinedione peroxisome proliferator-activated receptor γ agonist, FK614, ameliorates insulin resistance in Zucker fatty rats
Minoura, H.; Takeshita, S.; Kimura, C.; Hirosumi, J.; Takakura, S.; Kawamura, I.; Seki, J.; Manda, T.; Mutoh, S.
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收藏Ameliorating effect of FK614, a novel nonthiazolidinedione peroxisome proliferator-activated receptor γ agonist, on insulin resistance in Zucker fatty rat
Minoura, H; Takeshita, S; Yamamoto, T; Mabuchi, M; Hirosumi, J; Takakura, S; Kawamura, I; Seki, J; Manda, T; Ita, M; Mutoh, S
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收藏Prevention of progressive joint destruction in adjuvant induced arthritis in rats by a novel matrix metalloproteinase inhibitor, FR217840 (vol 508, pg 239, 2005)
Ishikawa, T; Nishigaki, F; Miyata, S; Hirayama, Y; Minoura, K; Imanishi, J; Neya, M; Mizutani, T; Imamura, Y; Ohkubo, Y; Mutoh, S
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收藏FK1706, a novel non-immunosuppressive immunophilin: neurotrophic activity and mechanism of action
Price, RD; Yamaji, T; Yamamoto, H; Higashi, Y; Hanaoka, K; Yamazaki, S; Ishiye, M; Aramori, I; Matsuoka, N; Mutoh, S; Yanagihara, T; Gold, BG
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收藏Discovery of quinazolinone and quinoxaline derivatives as potent and selective poly(ADP-ribose) polymerase-1/2 inhibitors喹唑啉酮和喹喔啉衍生物作为有效和选择性聚 (ADP-核糖) 聚合酶-1/2抑制剂的发现
Iwashita, A; Hattori, K; Yamamoto, H; Ishida, J; Kido, Y; Kamijo, K; Murano, K; Miyake, H; Kinoshita, T; Warizaya, M; Ohkubo, M; Matsuoka, N; Mutoh, S
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