Masakazu Sato

发表

Design, synthesis, and evaluation of novel 4-thiazolylimidazoles as inhibitors of transforming growth factor-β type I receptor kinase.

H. Amada, Y. Sekiguchi, N. Ono, 2012, Bioorganic & medicinal chemistry letters.

5-(1,3-Benzothiazol-6-yl)-4-(4-methyl-1,3-thiazol-2-yl)-1H-imidazole derivatives as potent and selective transforming growth factor-β type I receptor inhibitors.

H. Amada, Y. Sekiguchi, N. Ono, 2012, Bioorganic & medicinal chemistry.

Imidazole derivatives as new potent and selective 20-HETE synthase inhibitors.

Toshio Nakamura, H. Kakinuma, N. Miyata, 2004, Bioorganic & medicinal chemistry letters.

Beneficial Effects of a new 20-HETE Synthesis Inhibitor, TS-011, on Hemorrhagic and Ischemic Stroke

S. Okuyama, D. Harder, N. Miyata, 2005 .

Beneficial Effects of a New 20-Hydroxyeicosatetraenoic Acid Synthesis Inhibitor, TS-011 [N-(3-Chloro-4-morpholin-4-yl) Phenyl-N′-hydroxyimido Formamide], on Hemorrhagic and Ischemic Stroke

S. Okuyama, R. Roman, D. Harder, 2005, Journal of Pharmacology and Experimental Therapeutics.

Peyer's patch-immunomodulating glucans from sugar cane enhance protective immunity through stimulation of the hemopoietic system.

S. Ōmura, H. Kiyohara, K. Otoguro, 2019, International journal of biological macromolecules.

TU-572, a Potent and Selective CD45 Inhibitor, Suppresses IgE-Mediated Anaphylaxis and Murine Contact Hypersensitivity Reactions

T. Hamaguchi, H. Osada, Masakazu Sato, 2001, International Archives of Allergy and Immunology.

Effects of the novel and potent lymphocyte-specific protein tyrosine kinase inhibitor TKM0150 on mixed lymphocyte reaction and contact hypersensitivity in mice

Masakazu Sato, Tetsuo Takayama, A. Takaoka, 2010, Arzneimittelforschung.

Synthesis and evaluation of novel fluorinated sulotroban-related sulfonamide derivatives as thromboxane A2 receptor antagonists

J. Goto, Masakazu Sato, S. Jinno, 1995 .

Pyrazole and isoxazole derivatives as new, potent, and selective 20-hydroxy-5,8,11,14-eicosatetraenoic acid synthase inhibitors.

Toshio Nakamura, H. Kakinuma, N. Miyata, 2003, Journal of medicinal chemistry.

2-Acylimino-3-alkyl-3H-thiazoline derivatives: one-pot, three-component condensation synthesis of novel β-turn mimics

T. Ishii, Keiko Takahashi, Masakazu Sato, 2005 .

Ring-fused pyrazole derivatives as potent inhibitors of lymphocyte-specific kinase (Lck): Structure, synthesis, and SAR.

H. Amada, T. Koami, Fumiyasu Shiozawa, 2010, Bioorganic & medicinal chemistry letters.

Pyrrole derivatives as potent inhibitors of lymphocyte-specific kinase: Structure, synthesis, and SAR.

H. Amada, Fumiyasu Shiozawa, Mayumi Endo, 2010, Bioorganic & medicinal chemistry letters.

2-Acylimino-3-alkyl-3H-thiazoline Derivatives: One-Pot, Three-Component Condensation Synthesis of Novel β-Turn Mimics.

T. Ishii, Keiko Takahashi, Masakazu Sato, 2005 .

Synthesis of Aromatic Thioamide from Nitrile Without Handling of Gaseous Hydrogen Sulfide

Masakazu Sato, A. Manaka, 2005 .

Synthesis and characterization of a potent and selective protein tyrosine phosphatase inhibitor, 2-[(4-methylthiopyridin-2-yl)methylsulfinyl]benzimidazole

T. Hamaguchi, H. Osada, Masakazu Sato, 2000 .

UV–vis and fluorescence spectroscopic detection of anions by the conformational restriction of 2,2′-binaphthalene derivatives bearing thiourea groups through a methylene spacer

S. Kondo, Masakazu Sato, 2006 .

Synthesis and Characterization of a Novel Protein Tyrosine Phosphatase Inhibitor, 2-(Cyclobutylamino)- N- (2-Furylmethyl)-2-Thioxoacetamide

T. Ishii, T. Hamaguchi, H. Osada, 2005 .

Synthesis of 2- and 3-Nitrooxypropanol by Chemoselective Reduction of Methyl 2-and 3-Nitrooxypropionoate

A. Nakazato, Masakazu Sato, K. Hatayama, 1990 .

HET0016, a potent and selective inhibitor of 20‐HETE synthesizing enzyme

N. Miyata, Masakazu Sato, K. Taniguchi, 2001, British journal of pharmacology.

Synthesis and antibacterial activity of a novel series of acylides: 3-O-(3-pyridyl)acetylerythromycin A derivatives.

A. Nishida, Masakazu Sato, Hiroyuki Sugiyama, 2003, Journal of medicinal chemistry.

Pyrazole derivatives as new potent and selective 20-hydroxy-5,8,11,14-eicosatetraenoic acid synthase inhibitors.

Toshio Nakamura, H. Kakinuma, N. Miyata, 2004, Bioorganic & medicinal chemistry.

Design and synthesis of 1-(4-benzoylphenyl)imidazole derivatives as new potent 20-HETE synthase inhibitors.

T. Ishii, Toshio Nakamura, N. Miyata, 2004, Bioorganic & medicinal chemistry letters.

Design and Synthesis of 1‐(4‐Benzoylphenyl)imidazole Derivatives as New Potent 20‐HETE Synthase Inhibitors.

T. Ishii, Toshio Nakamura, N. Miyata, 2005 .

Discovery of a N'-hydroxyphenylformamidine derivative HET0016 as a potent and selective 20-HETE synthase inhibitor.

T. Ishii, M. Sato, N. Miyata, 2001, Bioorganic & medicinal chemistry letters.

Effects of the novel and potent lymphocyte-specific protein tyrosine kinase inhibitor TKM0150 on mixed lymphocyte reaction and contact hypersensitivity in mice

Masakazu Sato, Tetsuo Takayama, A. Takaoka, 2010, Arzneimittelforschung.

Isolation and Partial Characterization of an 87-Kilodalton 3-1 , 3-Glucanase from Bacillus circulans IAM 1165

K. Horikoshi, Mami Yamamoto, Masakazu Sato, 2022 .