Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Tomoko, Kuribara"'
Autor:
Keisuke Kitakaze, Shusuke Taniuchi, Eri Kawano, Yoshimasa Hamada, Masato Miyake, Miho Oyadomari, Hirotatsu Kojima, Hidetaka Kosako, Tomoko Kuribara, Suguru Yoshida, Takamitsu Hosoya, Seiichi Oyadomari
Publikováno v:
eLife, Vol 8 (2019)
The endoplasmic reticulum (ER) is responsible for folding secretory and membrane proteins, but disturbed ER proteostasis may lead to protein aggregation and subsequent cellular and clinical pathologies. Chemical chaperones have recently emerged as a
Externí odkaz:
https://doaj.org/article/08f2c99617734a8fa9aa3dfa44a5e62f
Autor:
Takamoto Morita, Yoshihiro Misawa, Yuka Koike, Isao Kii, Harumi Ito, Suguru Yoshida, Yuki Sakata, Takamitsu Hosoya, Tomoko Kuribara
Publikováno v:
Chemical Communications. 57:899-902
Efficient consecutive 1,2,3-triazole formations using multiazide platforms are disclosed. On the basis of unique clickability of the 1-adamantyl azido group, a four-step synthesis of tetrakis(triazole)s was achieved from a tetraazide platform molecul
Autor:
Yuki Sakata, Yasutomo Hatakeyama, Tomohiro Meguro, Keisuke Adachi, Kazunobu Igawa, Suguru Yoshida, Takamitsu Hosoya, Katsuhiko Tomooka, Tomoko Kuribara, Naoaki Makio
Publikováno v:
Chemical Communications. 56:11449-11452
A protection method for cycloalkynes by the formation of (hexafluoroacetylacetonato)copper(i)-cycloalkyne complexes is disclosed. Various complexes having functional groups were efficiently prepared, which are easily purified by silica-gel column chr
Autor:
Suguru Yoshida, Takamitsu Hosoya, Keisuke Kitakaze, Eri Kawano, Seiichi Oyadomari, Masato Miyake, Yoshimasa Hamada, Hidetaka Kosako, Hirotatsu Kojima, Shusuke Taniuchi, Tomoko Kuribara, Miho Oyadomari
Publikováno v:
The FASEB Journal. 35
Autor:
Takuya Kobayashi, Suguru Yoshida, Takamitsu Hosoya, Tomoko Kuribara, Tsubasa Matsuzawa, Kazushi Morimoto, Takamoto Morita
Publikováno v:
RSC Advances. 8:21754-21758
Various 2,3-disubstituted 6,7-thienobenzynes have been efficiently generated from the corresponding o-silylaryl triflate-type precursors by activation with fluoride ions. The method has expanded the scope of synthesizable multisubstituted benzothioph
Autor:
Hirotatsu Kojima, Takamitsu Hosoya, Seiichi Oyadomari, Masato Miyake, Hidetaka Kosako, Shusuke Taniuchi, Tomoko Kuribara, Suguru Yoshida, Keisuke Kitakaze, Eri Kawano, Yoshimasa Hamada, Miho Oyadomari
Publikováno v:
eLife
eLife, Vol 8 (2019)
eLife, Vol 8 (2019)
The endoplasmic reticulum (ER) is responsible for folding secretory and membrane proteins, but disturbed ER proteostasis may lead to protein aggregation and subsequent cellular and clinical pathologies. Chemical chaperones have recently emerged as a
Autor:
Masato Miyake, Keisuke Kitakaze, Hidetaka Kosako, Miho Oyadomari, Shusuke Taniuchi, Seiichi Oyadomari, Takamitsu Hosoya, Tomoko Kuribara, Hirotatsu Kojima, Eri Kawano, Suguru Yoshida, Yoshimasa Hamada
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbf8cc6c5363c5c24f1673c3535b6806
https://doi.org/10.7554/elife.43302.sa2
https://doi.org/10.7554/elife.43302.sa2
Autor:
Isao Kii, Fumika Karaki, Yoshitake Nishiyama, Harumi Ito, Suguru Yoshida, Tomohiro Meguro, Takamitsu Hosoya, Yuka Koike, Tomoko Kuribara, Yasutomo Hatakeyama
Publikováno v:
Chemical communications (Cambridge, England). 55(24)
A facile method for preparing various functional cycloalkynes, including proteins incorporated with a cycloalkyne moiety, from the corresponding azides is developed. Treatment of diynes bearing strained and terminal alkyne moieties with a copper salt
Autor:
Takamitsu Hosoya, Shusuke Taniuchi, Tomoko Kuribara, Keisuke Kitakaze, Masato Miyake, Hirotatsu Kojima, Eri Kawano, Suguru Yoshida, Hidetaka Kosako, Miho Oyadomari, Yoshimasa Hamada, Seiichi Oyadomari
Publikováno v:
Proceedings for Annual Meeting of The Japanese Pharmacological Society. 93:2-YIA
Autor:
Suguru, Yoshida, Tomoko, Kuribara, Takamoto, Morita, Tsubasa, Matsuzawa, Kazushi, Morimoto, Takuya, Kobayashi, Takamitsu, Hosoya
Publikováno v:
RSC advances. 8(39)
Various 2,3-disubstituted 6,7-thienobenzynes have been efficiently generated from the corresponding