Design and synthesis of Rho kinase inhibitors (II)

…, H Ohashi, M Sato, T Sugiyama, K Fukushima…

文献索引：Iwakubo, Masayuki; Takami, Atsuya; Okada, Yuji; Kawata, Takehisa; Tagami, Yoshimichi; Ohashi, Hiroshi; Sato, Motoko; Sugiyama, Terumi; Fukushima, Kayoko; Iijima, Hiroshi Bioorganic and Medicinal Chemistry, 2007 , vol. 15, # 1 p. 350 - 364

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被引用次数: 63

摘要

In a previous study, we identified several structurally unrelated scaffolds of the Rho kinase inhibitor using pharmacophore information obtained from the results of a high-throughput screening and structural information from a homology model of Rho kinase. 1H-Indazole is one of the candidate scaffolds on which a new series of potent Rho kinase inhibitors could be developed. In this study, the detailed structure–activity relationship of 1H-indazole ...