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Hiroyuki Kurihara

Nagaoka University of Technology

27

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821

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Studies of non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 2: synthesis and structure-activity relationships of 2-cyano and 2-hydroxy thiazolidenebenzenesulfonamide derivatives.

2005 Bioorganic & Medicinal Chemistry
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Erratum: Target-induced conformational adaptation of calmodulin revealed by the crystal structure of a complex with nematode Ca2+/calmodulin- dependent kinase kinase peptide (Journal of Molecular Biology (2001) 312 (59-68) DOI: 10.1006/jmbi.2001.4822)

2005 Journal of Molecular Biology
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Studies of nonnucleoside HIV-1 reverse transcriptase inhibitors. Part 1: Design and synthesis of thiazolidenebenzenesulfonamides

2004 Bioorganic & Medicinal Chemistry
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Design, synthesis and biological activity of YM-60828 derivatives. Part 2: potent and orally-bioavailable factor Xa inhibitors based on benzothiadiazine-4-one template

2003 Bioorganic & Medicinal Chemistry
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The discovery of YM-60828: a potent, selective and orally-bioavailable factor Xa inhibitor.

2002 Bioorganic & Medicinal Chemistry
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Design, synthesis and biological activity of YM-60828 derivatives: potent and orally-bioavailable factor Xa inhibitors based on naphthoanilide and naphthalensulfonanilide templates.

2002 Bioorganic & Medicinal Chemistry
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Coumarin and chromen-4-one analogues as tautomerase inhibitors of macrophage migration inhibitory factor: discovery and X-ray crystallography.

2001 Journal of Medicinal Chemistry
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Target-induced conformational adaptation of calmodulin revealed by the crystal structure of a complex with nematode Ca(2+)/calmodulin-dependent kinase kinase peptide

2001 Journal of Molecular Biology
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Target-induced Conformational Adaptation of Calmodulin Revealed by the Crystal Structure of a Complex with Nematode Ca 2á /Calmodulin-dependent

2001
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Design of the Y1‐receptor‐selective cyclic peptide based on the C‐terminal sequence of neuropeptide Y

2000 Journal of Peptide Research
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Citations (5)