Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kaori Takama"'
Autor:
Masato Ohbuchi, Kaori Takama, Shunji Yamazaki, Akira Fujimori, Kazuhiro Tetsuka, Takayuki Goto, Fumiko Kiyonaga, Tetsuhiro Kawabe
Publikováno v:
Biologicalpharmaceutical bulletin. 43(3)
Recent progress in the fields of tissue engineering, micro-electro mechanical systems, and materials science have greatly improved cell culture systems, which were traditionally performed in a static two-dimensional manner. This progress has led to a
Autor:
Takeshi Nakamura, Kaori Takama, Dorien Groenendaal, Radboud van Trigt, Yoshiaki Ohtsu, Kiyoshi Noguchi, Akitsugu Takada
Publikováno v:
Chromatographia. 80:217-227
This is a case study of the difficulties caused by supersaturation of an analyte during the quantification of a drug in urine. To support the clinical development of the potent helicase–primase inhibitor ASP2151, we developed and validated simple a
Autor:
Wataru Hamaguchi, Kaori Takama, Kiyohiro Samizu, Takuma Mihara, Naoyuki Masuda, Toshihiro Watanabe
Publikováno v:
Chemical and Pharmaceutical Bulletin. 62:1200-1213
A novel class of phosphodiesterase 10A (PDE10A) inhibitors with improved metabolic stability in mouse liver microsomes were designed and synthesized starting from 2-({4-[1-methyl-4-(pyridin-4-yl)-1H-pyrazol-3-yl]phenoxy}methyl)quinoline (MP-10). Repl
Autor:
Tomomi Furihata, Kaori Takama, Kaoru Kobayashi, Kan Chiba, Tomoaki Higuchi, Masakiyo Hosokawa, Sachiyo Kawashima
Publikováno v:
Drug Metabolism and Disposition. 34:1012-1018
CYP2C9 and CYP2C19 are clinically important drug-metabolizing enzymes. The expression level of CYP2C9 is much higher than that of CYP2C19, although the factor(s) responsible for the difference between the expression levels of these genes is still unc
Autor:
Wataru, Hamaguchi, Naoyuki, Masuda, Kiyohiro, Samizu, Takuma, Mihara, Kaori, Takama, Toshihiro, Watanabe
Publikováno v:
Chemicalpharmaceutical bulletin. 62(12)
A novel class of phosphodiesterase 10A (PDE10A) inhibitors with improved metabolic stability in mouse liver microsomes were designed and synthesized starting from 2-({4-[1-methyl-4-(pyridin-4-yl)-1H-pyrazol-3-yl]phenoxy}methyl)quinoline (MP-10). Repl