Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Tomohiko Ueda"'
Autor:
Nahoko Uchiyama, Kohei Kiyota, Junko Hosoe, Takanori Komatsu, Naoki Sugimoto, Kyoko Ishizuki, Tatsuo Koide, Mika Murabayashi, Kengo Kobayashi, Yoshinori Fujimine, Toshiyuki Yokose, Katsuya Ofuji, Hitoshi Shimizu, Takashi Hasebe, Yumi Asai, Eri Ena, Junko Kikuchi, Kazuhiro Fujita, Yoshinobu Makino, Yoshiaki Iwamoto, Toru Miura, Yasuhiro Muto, Katsuo Asakura, Takako Suematsu, Hitomi Muto, Ai Kohama, Takashi Goto, Masu Yasuda, Tomohiko Ueda, Yukihiro Goda
Publikováno v:
Chemical and Pharmaceutical Bulletin. 70:892-900
Autor:
Nahoko, Uchiyama, Kohei, Kiyota, Junko, Hosoe, Takanori, Komatsu, Naoki, Sugimoto, Kyoko, Ishizuki, Tatsuo, Koide, Mika, Murabayashi, Kengo, Kobayashi, Yoshinori, Fujimine, Toshiyuki, Yokose, Katsuya, Ofuji, Hitoshi, Shimizu, Takashi, Hasebe, Yumi, Asai, Eri, Ena, Junko, Kikuchi, Kazuhiro, Fujita, Yoshinobu, Makino, Yoshiaki, Iwamoto, Toru, Miura, Yasuhiro, Muto, Katsuo, Asakura, Takako, Suematsu, Hitomi, Muto, Ai, Kohama, Takashi, Goto, Masu, Yasuda, Tomohiko, Ueda, Yukihiro, Goda
Publikováno v:
Chemicalpharmaceutical bulletin. 70(12)
Quantitative
Autor:
Eri Ena, Naoki Sugimoto, Yoshinobu Makino, Hitomi Muto, Yoshiaki Iwamoto, Masu Yasuda, Tomohiko Ueda, Mika Murabayashi, Takako Suematsu, Koji Mizui, Hitoshi Shimizu, Tatsuo Koide, Ai Kohama, Junko Kikuchi, Takashi Hasebe, Toru Miura, Kohei Kiyota, Nahoko Uchiyama, Takashi Goto, Yoshinori Fujimine, Yukihiro Goda, Kyoko Ishizuki, Toshiyuki Yokose, Junko Hosoe, Kazuhiro Fujita, Kengo Kobayashi, Yumi Asai, Naoko Yasobu, Katsuo Asakura, Katsuya Ofuji, Naoto Miyashita
Publikováno v:
Chemical and Pharmaceutical Bulletin. 69:630-638
Recently, quantitative NMR (qNMR), especially 1H-qNMR, has been widely used to determine the absolute quantitative value of organic molecules. We previously reported an optimal and reproducible sample preparation method for 1H-qNMR. In the present st
Autor:
Nahoko, Uchiyama, Junko, Hosoe, Naoki, Sugimoto, Kyoko, Ishizuki, Tatsuo, Koide, Mika, Murabayashi, Naoto, Miyashita, Kengo, Kobayashi, Yoshinori, Fujimine, Toshiyuki, Yokose, Katsuya, Ofuji, Hitoshi, Shimizu, Takashi, Hasebe, Yumi, Asai, Eri, Ena, Junko, Kikuchi, Kohei, Kiyota, Kazuhiro, Fujita, Yoshinobu, Makino, Naoko, Yasobu, Yoshiaki, Iwamoto, Toru, Miura, Koji, Mizui, Katsuo, Asakura, Takako, Suematsu, Hitomi, Muto, Ai, Kohama, Takashi, Goto, Masu, Yasuda, Tomohiko, Ueda, Yukihiro, Goda
Publikováno v:
Chemicalpharmaceutical bulletin. 69(7)
Recently, quantitative NMR (qNMR), especially
Publikováno v:
Chemical and Pharmaceutical Bulletin. 57:1096-1099
Formaldehyde is a well-known air impurity. The possibility was investigated in this study that pharmaceutical excipients commonly used in oral solid dosage forms might also be sources of formaldehyde. The results showed that formaldehyde is generated
Publikováno v:
IEICE Transactions on Electronics. :896-903
This paper reports on the bending loss insensitive single mode fiber suitable for access networks, which is applicable for wide wavelength use. Excellent attenuation stability of the fiber in the full spectrum range has been confirmed even in severe
Autor:
Tomohiko Ueda, Kazuya Matsumoto, Teruaki Une, Hiroshi Toda, Masato Sakamoto, Kenji Suzuki, Takeshi Ochi, Akira Minamida, Yoshiaki Terauchi
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 15:1055-1059
Two major metabolites in humans of blonanserin, 2-(4-ethyl-1-piperazinyl)-4-(4-fluorophenyl)-5,6,7,8,9,10-hexahydrocycloocta-[b]pyridine (code name AD-5423), were synthesized. The first, 7-hydroxylated AD-5423, was synthesized through a four-step pro
Autor:
Yuuki Awa, Kazuo Nagai, Masaaki Wachi, Junichi Yamagishi, Noritaka Iwai, Tomohiko Ueda, Shoji Asano, Kenji Suzuki
Publikováno v:
Bioscience, Biotechnology, and Biochemistry. 69:1721-1725
A new antibiotic, which is structurally related to 5-aminolevulinic acid, a precursor of heme biosynthesis, and named alaremycin, was isolated from the culture broth of an actinomycete strain through a random screening with the blue assay to detect t
Autor:
Junichi Yamagishi, Tomohiko Ueda, Hideo Terauchi, Keiko Ofuji, Kenji Suzuki, Motoji Kawasaki, Mika Fujimoto, Masaaki Wachi, Akihiko Tanitame, Kazuo Nagai, Yoshihiro Oyamada
Publikováno v:
Bioorg. Med. Chem.. 12(No. 21):5515-5524
The 4-piperidyl moiety and the pyrazole ring in 1-(3-chlorophenyl)-5-(4-phenoxyphenyl)-3-(4-piperidyl)pyrazole 2 , which has previously shown improved DNA gyrase inhibition and target-related antibacterial activity, were transformed to other groups a
Autor:
Tomohiko, Ueda, Hiroshi, Abe
Publikováno v:
學苑 = GAKUEN. 736:107-116