Y. Yamazaki

发表

Synthesis of highly deuterium-labeled (R)-K-13675, PPAR alpha agonist, for use as an internal standard for low-level quantification of drugs in plasma.

K. Shibuya, Y. Yamazaki, S. Ogawa, 2009, Bioorganic & medicinal chemistry.

A practical synthesis of the PPARα agonist, (R)-K-13675, starting from (S)-2-hydroxybutyrolactone

Takaaki Araki, K. Shibuya, Y. Yamazaki, 2008 .

Design and synthesis of highly potent and selective human peroxisome proliferator-activated receptor alpha agonists.

B. Staels, J. Fruchart, Takaaki Araki, 2007, Bioorganic & Medicinal Chemistry Letters.

Design and synthesis of highly potent and selective human peroxisome proliferator-activated receptor alpha agonists.

B. Staels, J. Fruchart, Keisuke Inoue, 2007, Bioorganic & medicinal chemistry letters.

A practical synthesis for (S)-5-(4-(1-methylethoxy)phenyl)-5-methylimidazolidine-2,4-dione and its application in the synthesis of a novel liver X receptor β-selective agonist

K. Shibuya, Y. Yamazaki, Minoru Koura, 2016 .

A facile method for converting alcohol to thioether and its application in the synthesis of a novel GPR119 agonist

Tomoaki Koshizawa, K. Shibuya, Y. Yamazaki, 2015 .

Lipase-catalyzed enantiosynthesis of (R)- and (S)-2-[benzyl(phenyl)amino]ethyl 5-(5,5-dimethyl-2-oxo-1,3,2-dioxaphosphorinan-2-yl)-1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3-pyridinecarboxylate (NZ 105)

K. Achiwa, H. Ebiike, Y. Yamazaki, 1995 .

A Study into the ADP-Ribosylome of IFN-γ-Stimulated THP-1 Human Macrophage-like Cells Identifies ARTD8/PARP14 and ARTD9/PARP9 ADP-Ribosylation

Sasha A. Singh, M. Aikawa, T. Maejima, 2019, Journal of proteome research.

Lipase-Catalyzed Enantioselective Hydrolysis of Bis(acyloxymethyl) 1, 4-Dihydro-3, 5-pyridinedicarboxylates Leading to Optically Active Medicines

K. Achiwa, Hirose Yoshihiko, Kariya Kinya, 1997 .

Multi-organ systems study reveals Igfbp7 as a suppressor of gluconeogenesis after gastric bypass surgery.

Jose-Luiz Figueiredo, Sasha A. Singh, M. Aikawa, 2020, Journal of proteome research.

Novel Synthesis of Butyl (S)-2-Hydroxybutanoate, the Key Intermediate of PPARα Agonist (R)-K-13675 from Butyl (2S,3R)-Epoxybutanoate and Butyl (S)-2,3-Epoxypropanoate

Takaaki Araki, K. Shibuya, Y. Yamazaki, 2013 .