K. Honbou

发表

Crystallization and preliminary crystallographic analysis of DJ-1, a protein associated with male fertility and parkinsonism.

T. Niki, T. Taira, H. Ariga, 2003, Acta crystallographica. Section D, Biological crystallography.

clinically-used ARBs: drug-target interaction analyses

M. Orita, Tomohiko Yamaguchi, H. Masuzaki, 2014 .

Distinct Properties of Telmisartan on Agonistic Activities for Peroxisome Proliferator-Activated Receptor γ among Clinically Used Angiotensin II Receptor Blockers: Drug-Target Interaction Analyses

M. Orita, Tomohiko Yamaguchi, H. Masuzaki, 2014, The Journal of Pharmacology and Experimental Therapeutics.

Crystallization of Saccharomyces cerevisiae alpha-mannosidase, a cargo protein of the Cvt pathway.

F. Inagaki, N. Noda, Y. Ohsumi, 2009, Acta crystallographica. Section F, Structural biology and crystallization communications.

Crystallization and preliminary crystallographic analysis of p40phox, a regulatory subunit of NADPH oxidase.

F. Inagaki, S. Yuzawa, Y. Fujioka, 2006, Acta crystallographica. Section F, Structural biology and crystallization communications.

The Domain Organization of p67phox, a Protein Required for Activation of the Superoxide-Producing NADPH Oxidase in Phagocytes

F. Inagaki, S. Yuzawa, H. Sumimoto, 2009, Journal of Innate Immunity.

Fragment-Based Discovery of Pyrimido[1,2-b]indazole PDE10A Inhibitors.

T. Mihara, Y. Amano, I. Namatame, 2018, Chemical & pharmaceutical bulletin.

Novel benzimidazole derivatives as phosphodiesterase 10A (PDE10A) inhibitors with improved metabolic stability.

T. Mihara, Y. Amano, M. Yamazaki, 2014, Bioorganic & medicinal chemistry.

Design and synthesis of novel benzimidazole derivatives as phosphodiesterase 10A inhibitors with reduced CYP1A2 inhibition.

S. Kikuchi, Toshihiro Watanabe, T. Mihara, 2013, Bioorganic & medicinal chemistry.

Full‐length p40phox structure suggests a basis for regulation mechanism of its membrane binding

F. Inagaki, S. Yuzawa, H. Sumimoto, 2007, The EMBO journal.

Synthesis, SAR study, and biological evaluation of novel quinoline derivatives as phosphodiesterase 10A inhibitors with reduced CYP3A4 inhibition.

S. Kikuchi, T. Mihara, K. Hattori, 2015, Bioorganic & medicinal chemistry.

The Crystal Structure of DJ-1, a Protein Related to Male Fertility and Parkinson's Disease*

T. Niki, T. Taira, H. Ariga, 2003, Journal of Biological Chemistry.

Distinct Properties of Telmisartan on Agonistic Activities for Peroxisome Proliferator-Activated Receptor γ among Clinically Used Angiotensin II Receptor Blockers: Drug-Target Interaction Analyses

M. Orita, Tomohiko Yamaguchi, H. Masuzaki, 2014, The Journal of Pharmacology and Experimental Therapeutics.

The Domain Organization of p67phox, a Protein Required for Activation of the Superoxide-Producing NADPH Oxidase in Phagocytes

F. Inagaki, S. Yuzawa, H. Sumimoto, 2009, Journal of Innate Immunity.

The crystal structure of NADPH binding domain of gp91(phox)

K. Honbou, 2010 .