Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Toshiyuki Shimazaki"'
Publikováno v:
情報処理学会論文誌 教育とコンピュータ(TCE). 8(2):51-63
本研究では,本学学内における対面での利用のみを想定して作成されていた実験システムを,やむを得ない理由で遠隔対応させ使用した結果,教育にどのような影響を及ぼしたかを調査
Publikováno v:
Learning and Collaboration Technologies. Novel Technological Environments ISBN: 9783031056741
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f779f37bacae1011ea68b3aa6e203d65
https://doi.org/10.1007/978-3-031-05675-8_17
https://doi.org/10.1007/978-3-031-05675-8_17
Autor:
Yoko Usui, Toshiyuki Shimazaki, Terunori Fujita, Haruyuki Makio, Takashi Ochiai, Sadahiko Matsuura, Junichi Mohri, Kouji Takeda
Publikováno v:
Journal of the American Chemical Society. 135:8177-8180
Multinuclear alkylene zinc (MAZ) compounds of the type EtZn-(R″-Zn)n-Et (R″ = ethyl and propyl branched alkylene groups) were synthesized by a simple one-step procedure in nonpolar hydrocarbon solvents from α,ω-dienes (e.g., 1,7-octadiene or 1,
Autor:
Kunio Okumura, Toshiyuki Shimazaki, Kouhei Yazawa, Eishi Tanaka, Yoji Aoki, Shinichi Banba, Hiroyuki Yamashita, Kenji Kibayashi, Hitoshi Banno
Publikováno v:
Journal of Medicinal Chemistry. 41:4036-4052
The design, synthesis, and pharmacological evaluation of (S)-(-)-ethyl [6-[4-(morpholinoformimidoyl)benzamido]-3, 4-dihydro-2H-1-benzopyran-3-yl]acetate hydrochloride ((S)-4.HCl, MS-180), an orally active glycoprotein IIb-IIIa (GPIIb-IIIa) antagonist
Publikováno v:
IEEJ Transactions on Fundamentals and Materials. 114:710-717
Autor:
Toshiyuki Shimazaki, Yoshihide Manabe
Publikováno v:
IEEJ Transactions on Fundamentals and Materials. 110:77-84
Publikováno v:
Journal of Organic Chemistry. 55(No. 19):5324-5335
Autor:
Hiroyuki, Seimiya, Tomoko, Oh-hara, Tsuneji, Suzuki, Imad, Naasani, Toshiyuki, Shimazaki, Katsutoshi, Tsuchiya, Takashi, Tsuruo
Publikováno v:
Molecular cancer therapeutics. 1(9)
Epidemiological studies suggest potent anticancer effects of tea catechins. Previously, we have reported (I. Naasani et aL, Biochem. Biophys. Res. Commun., 249: 391-396, 1998) that epigallocatechin gallate (EGCG), a major tea catechin, strongly and d
Autor:
Fumie Sato, Yousuke Seyama, Yuichi Kobayashi, Keiko Kawajiri, Toshiyuki Shimazaki, Takao Shimizu
Publikováno v:
Biochimica et biophysica acta. 1215(3)
In order to examine a role of the C(16)–C(20) methylene part of leukotriene B4 (LTB4) toward the activation of leukocytes, we synthesized the LTB4-analogues in which the length of the C(16)–C(20) part of LTB4 is varied systematically while the tw
Publikováno v:
Tetrahedron Letters. 28:3959-3962
Both enantiomers of coriolic acid and their geometric isomers are synthesized highly selectively. These acids are found to exhibit similar inhibition activity toward spore germination of rice blast fungus.