Search Results - "FUKUSHIMA, Kayoko"

Design and synthesis of Rho kinase inhibitors (II) by Iwakubo, Masayuki, Takami, Atsuya, Okada, Yuji, Kawata, Takehisa, Tagami, Yoshimichi, Ohashi, Hiroshi, Sato, Motoko, Sugiyama, Terumi, Fukushima, Kayoko, Iijima, Hiroshi

“…Optimization of the 1 H-indazole Rho kinase inhibitors resulted in improvements of the solubility and the inhibitory potency for chemotaxis. In a previous…”
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Design and synthesis of rho kinase inhibitors (III) by Iwakubo, Masayuki, Takami, Atsuya, Okada, Yuji, Kawata, Takehisa, Tagami, Yoshimichi, Sato, Motoko, Sugiyama, Terumi, Fukushima, Kayoko, Taya, Shinichiro, Amano, Mutsuki, Kaibuchi, Kozo, Iijima, Hiroshi

“…N-(1-benzyl-3-pyrrolidyl)- N-(5-isoquinolyl)amine analogues were optimized efficacy based on the in vitro Rho kinase inhibition, the cell-based chemotaxis…”
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Design and synthesis of Rho kinase inhibitors (I) by Takami, Atsuya, Iwakubo, Masayuki, Okada, Yuji, Kawata, Takehisa, Odai, Hideharu, Takahashi, Nobuaki, Shindo, Kazutoshi, Kimura, Kaname, Tagami, Yoshimichi, Miyake, Mika, Fukushima, Kayoko, Inagaki, Masaki, Amano, Mutsuki, Kaibuchi, Kozo, Iijima, Hiroshi

“…Structure-based design of several scaffolds of Rho kinase inhibitor was performed by using pharmacophore information obtained from a high-throughput screening…”
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Orally active anti-proliferation agents : Novel diphenylamine derivatives as FGF-R2 autophosphorylation inhibitors by SHIMIZU, Toshiyuki, FUJIWARA, Yasunari, IWAI, Akemi, FUKUSHIMA, Kayoko, YOSHINO, Tetsuya, MIWA, Atsushi, OSAWA, Tatsushi, SAKAI, Teruyuki, KUBO, Kinya, KUBO, Kazuo, NISHITOBA, Tsuyoshi, KIMURA, Kaname, SENGA, Terufumi, MUROOKA, Hideko

“…(6,7-Disubstituted-quinolin-4-yloxy-phenyl)(4-substituted-phenyl)amine derivatives were synthesized and evaluated by a cellular autophosphorylation assay for…”
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Studies on plants containing indole alkaloids. VIII. Indole alkaloid glycosides and other constituents of the leaves of Uncaria rhynchophylla Miq by Aimi, N, Shito, T, Fukushima, K, Itai, Y, Aoyama, C

“…A new glycoindole alkaloid, rhynchophine, was isolated from the leaves of Uncaria rhynchophylla MIQ. and its structure was elucidated as 6'-feruloyl vincoside…”
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Corrigendum to “Design and synthesis of Rho kinase inhibitors (I)”: [Bioorg. Med. Chem. 12 (2004) 2115] by Takami, Atsuya, Iwakubo, Masayuki, Okada, Yuji, Kawata, Takehisa, Odai, Hideharu, Takahashi, Nobuaki, Shindo, Kazutoshi, Kimura, Kaname, Tagami, Yoshimichi, Miyake, Mika, Fukushima, Kayoko, Inagaki, Masaki, Amano, Mutsuki, Kaibuchi, Kozo, Iijima, Hiroshi

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