N. Katayama

发表

Identification of a key element for hydrogen‐bonding patterns between protein kinases and their inhibitors

H. Hisamichi, S. Kuromitsu, S. Fujita, 2008, Proteins.

Discovery of an 8-methoxytetrahydroisoquinoline derivative as an orally active N-type calcium channel blocker for neuropathic pain without CYP inhibition liability.

M. Inoue, Toshihiro Watanabe, N. Katayama, 2015, Bioorganic & medicinal chemistry.

Synthesis and pharmacological evaluation of bis-3-(3,4-dichlorophenyl)acrylamide derivatives as glycogen phosphorylase inhibitors.

K. Onda, K. Momose, M. Orita, 2008, Bioorganic & medicinal chemistry.

Coexistence of TDP‐43 and tau pathology in neurodegeneration with brain iron accumulation type 1 (NBIA‐1, formerly Hallervorden‐Spatz syndrome)

S. Terada, Y. Uchitomi, O. Yokota, 2011, Neuropathology : official journal of the Japanese Society of Neuropathology.

Design, synthesis, and pharmacological evaluation of N-bicyclo-5-chloro-1H-indole-2-carboxamide derivatives as potent glycogen phosphorylase inhibitors.

K. Onda, K. Momose, M. Orita, 2008, Bioorganic & medicinal chemistry.

HUMAN MACROPHAGE MIGRATION INHIBITORY FACTOR (MIF)

H. Kurihara, N. Katayama, 2001 .

Macrophage migration inhibitory factor and the discovery of tautomerase inhibitors.

M. Orita, Satoshi Yamamoto, N. Katayama, 2002, Current pharmaceutical design.

Synthesis and biological activity of novel 1,2-disubstituted benzene derivatives as factor Xa inhibitors.

N. Katayama, Y. Matsumoto, Y. Iwatsuki, 2005, Bioorganic & medicinal chemistry.

The discovery of YM-60828: a potent, selective and orally-bioavailable factor Xa inhibitor.

H. Kurihara, N. Katayama, Y. Matsumoto, 2002, Bioorganic & medicinal chemistry.

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

H. Kurihara, N. Katayama, Y. Matsumoto, 2002, Bioorganic & medicinal chemistry.

The discovery of YM-60828: a potent, selective and orally-bioavailable factor Xa inhibitor.

H. Kurihara, N. Katayama, Y. Matsumoto, 2002, Bioorganic & Medicinal Chemistry.

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

S. Yamamoto, T. Yamada, M. Orita, 2001, Journal of medicinal chemistry.

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

M Ikura, M B Swindells, M. Swindells, 2001, Journal of molecular biology.

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

Masanori Osawa, Mitsuhiko Ikura, Mark B. Swindells, 2001 .

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

H. Kurihara, N. Katayama, Y. Matsumoto, 2003, Bioorganic & medicinal chemistry.

D-3-hydroxybutyrate dehydrogenase from Pseudomonas fragi: molecular cloning of the enzyme gene and crystal structure of the enzyme.

T. Yoshimoto, Y. Nakajima, Kiyoshi Ito, 2006, Journal of molecular biology.

Quantitative analysis of aggregation-solubility relationship by in-silico solubility prediction

Haruki Nakamura, Yoshifumi Fukunishi, Masaya Orita, 2010 .

Synthesis of 5-chloro-N-aryl-1H-indole-2-carboxamide derivatives as inhibitors of human liver glycogen phosphorylase a.

K. Onda, K. Negoro, K. Momose, 2008, Bioorganic & medicinal chemistry.

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)

M. Swindells, H. Tokumitsu, M. Ikura, 2005 .

Preliminary X‐ray crystallographic studies of photosynthetic reaction center from a thermophilic sulfur bacterium, Chromatium tepidum

K. Inaka, K. Miki, M. Kobayashi, 1994, FEBS letters.