Výsledky vyhledávání - "Mitsuji, Yamashita"

Akademický článek

Transcriptional repression of Cdc25B by IER5 inhibits the proliferation of leukemic progenitor cells through NF-YB and p300 in acute myeloid leukemia.

Autor: Satoki Nakamura, Yasuyuki Nagata, Lin Tan, Tomonari Takemura, Kiyoshi Shibata, Michio Fujie, Shinya Fujisawa, Yasutaka Tanaka, Mitsuo Toda, Reiko Makita, Kenji Tsunekawa, Manabu Yamada, Mayumi Yamaoka, Junko Yamashita, Kazunori Ohnishi, Mitsuji Yamashita

Publikováno v: PLoS ONE, Vol 6, Iss 11, p e28011 (2011)

The immediately-early response gene 5 (IER5) has been reported to be induced by γ-ray irradiation and to play a role in the induction of cell death caused by radiation. We previously identified IER5 as one of the 2,3,4-tribromo-3-methyl-1-phenylphos

Externí odkaz: https://doaj.org/article/f162a3b53d8940129ebf52cae39d9851

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Research on Phospha Sugar Analogues to Develop Novel Multiple Type Molecular Targeted Antitumor Drugs Against Various Types of Tumor Cells

Autor: Yasuhiro Magata, Mitsuo Toda, Michio Fujie, Keita Kiyofuji, Reiko Makita, Junko Yamashita, Satoki Nakamura, Kazuhide Asai, Haruhiko Sugimura, Mitsuji Yamashita, Yasutaka Tanaka, Mayumi Yamaoka, Manabu Yamada, Kenji Tsunekawa, Takuya Suyama, Kazunori Ohnishi

Publikováno v: Phosphorus, Sulfur, and Silicon and the Related Elements. 188:213-223

The synthesis and antitumor activity evaluation of new branched phospha sugars, especially deoxybromophospha sugar derivatives or bromophospholanes of 2,3-dibromo-3-methyl-1-phenylphospholane 1-oxide (DBMPP: 3) and 2,3,4-tribromo-3-methyl-1- phenylph

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::92e8d8ce831d54eae83a6e5cf9081bf7
https://doi.org/10.1080/10426507.2012.744016

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Synthesis and evaluation of novel phosphasugar anticancer agents

Autor: Mayumi Yamaoka, Nobuhisa Ozaki, Keita Kiyofuji, Satoki Nakamura, Junko Yamashita, Akiho Sawada, Mitsuji Yamashita, Kazuhide Asai, Mitsuo Toda, Masaki Sugiyama, Taishi Niimi, Manabu Yamada, Reiko Makita, Michio Fujie, Takuya Suyama, Kazunori Ohnishi

Publikováno v: Pure and Applied Chemistry. 84:37-48

Starting materials of phosphasugars, 1-phenyl-2-phospholene 1-oxides, were prepared from dienes and phenylphosphonous dichloride (dichlorophenylphosphine). Several substituted novel phosphasugars (3- or 4-halo-substituted)-1-phenyl-2-phospholene 1-ox

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::58d5701661e00fe84110ab816dfe82fd
https://doi.org/10.1351/pac-con-11-10-09

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Preparation of Phospha Sugar Analogues and Their Evaluation as Novel Molecular Targeting Anticancer Agents

Autor: Michio Fujie, Taishi Niimi, Kenji Tsunekawa, Satoru Ito, Junko Yamashita, Nobuhisa Ozaki, Satoki Nakamura, Manabu Yamada, Kazuhide Asai, Takuya Suyama, Mitsuji Yamashita

Publikováno v: Phosphorus, Sulfur, and Silicon and the Related Elements. 186:936-944

Phospha sugars were prepared by a novel synthetic route starting from phosphorus heterocyclic compounds, 2-phospholenes. The anhydro- and deoxy-phospha sugar derivatives have been revealed to have potential anticancer activities against human leukemi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d18326030263c06022f051902820cb80
https://doi.org/10.1080/10426507.2010.530326

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Preparation and Characterization of Phospha Sugar Analogues, 2,3-Dibromo-3-methyl-1- phenylphospholane 1-Oxide Derivatives, as Novel Anticancer Agents

Autor: Junko Yamashita, Manabu Yamada, Michio Fujie, Mitsuji Yamashita, Takuya Suyama, Taishi Niimi, Satoki Nakamura, Kazuhide Asai, Kasthuraiah Maddali

Publikováno v: Phosphorus, Sulfur, and Silicon and the Related Elements. 185:2286-2291

The synthesis of new phospha sugar analogues or phosphorus heterocycles and their biological activities as novel anticancer agents are reported in this article. A 1,2-dibromo-1,2-dideoxy phospha sugar derivative, 2,3-dibromo-3-methyl-1-phenylphosphol

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3ad0aa908aa8dae3b1103f0eb075622b
https://doi.org/10.1080/10426501003598622

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