Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Fumiya Mito"'
Publikováno v:
Asian Journal of Organic Chemistry. 2:388-391
Publikováno v:
Free Radical Biology and Medicine. 53:2112-2118
Ascorbic acid is a small-molecule reductant with multiple functions in vivo. Reducing ascorbic acid intake leads to a lack of hydroxylation of prolines and lysines, causing a looser triple helix and resulting in scurvy. Ascorbic acid also acts as an
Autor:
Hiroshi Hirata, Fumiya Mito, Miho C. Emoto, Hideo Sato-Akaba, Toshihide Yamasaki, Ken Ichi Yamada, Hirotada Fujii
Publikováno v:
Free Radical Research. 45:1325-1332
The loss of paramagnetism of nitroxide radicals due to reductant reactions in biological systems, places a fundamental time constraint on their application as an imaging probe in in vivo EPR imaging studies. However, in vitro studies of the newly syn
Autor:
Yuko Ito, Mayumi Yamato, Toshihide Yamasaki, Fumiya Mito, Ken Ichi Yamada, Chisato Shirahama, Kana Kitagawa, Taketoshi Oishi
Publikováno v:
Free Radical Research. 45:1103-1110
Lipid-derived radicals and peroxides are involved in the pathogenesis of oxidative stress diseases and, although lipid peroxide production is a required reaction between a lipid radical and molecular oxygen, a useful lipid radical detection method ha
Autor:
Kana Kitagawa, Yuta Matsuoka, Toshihide Yamasaki, Ken Ichi Yamada, Fumiya Mito, Yuko Ito, Mayumi Yamato
Publikováno v:
The Journal of Organic Chemistry. 76:4144-4148
Nitroxides have antioxidative activities toward lipid peroxidation, but the influence of steric factors is not known. We synthesized alkyl-substituted nitroxides at the α-position of the N-O moiety to enhance lipophilicity and the bulk effect. There
Autor:
Toshihide Yamasaki, Ken Ichi Yamada, Yuko Ito, Yuichi Kinoshita, Sokkar Pandian, Kiyoshi Sakai, Ramachandran Murugesan, Hideo Utsumi, Koji Nakano, Fumiya Mito
Publikováno v:
The Journal of Organic Chemistry. 76:435-440
We have synthesized several nitroxides with different substituents which vary the steric and electronic environment around the N-O moiety and have systematically investigated the role of substituents on the stability of the radicals. Our results demo
Autor:
Chisato Shirahama, Kiyoshi Sakai, Toshihide Yamasaki, Yuko Ito, Mayumi Yamato, Yuichi Kinoshita, Fumiya Mito, Ken Ichi Yamada, Hisato Deguchi, Hideo Utsumi, Nobuhisa Okukado, Nuttavut Kosem, Kana Kitagawa
Publikováno v:
Free Radical Biology and Medicine. 49:1703-1709
Nitroxyl radicals (nitroxide) have great potential advantages as spin probes, antioxidants, contrast agents, and radiation-protecting agents. However, they are readily reduced by reductants in cells and lose their paramagnetic nature. Recently, tetra
Autor:
Toshihide Yamasaki, Yuichi Kinoshita, Kiyoshi Sakai, Fumiya Mito, Hideo Utsumi, Ken Ichi Yamada
Publikováno v:
Tetrahedron. 66:2311-2315
Nitroxyl radicals (nitroxides) with unpaired electron are widely used as antioxidants, contrast agents, and spin probes. Although piperidine nitroxyl radicals have many applications, these are mainly tetramethylpiperidine compounds, and only a few re
Publikováno v:
ChemInform. 44
Nitroxides are stable free radicals which have the >N-O moiety. In most cases, nitroxides have a ring structure. For example, imidazoline, isoindoline, piperidine and pyrrolidine ring nitroxides (Fig. 1) have been used as agents for spin labeling, im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::935d33350118d1ac811e35709c71c16d
https://doi.org/10.5772/39163
https://doi.org/10.5772/39163