Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Takumi Daino"'
Autor:
Youichi Yachida, Motoi Kashiwagi, Takeshi Mikami, Keiko Tsuchihashi, Takumi Daino, Toyoaki Akino, Shinsei Gasa
Publikováno v:
Journal of Lipid Research, Vol 40, Iss 12, Pp 2271-2278 (1999)
A novel galactosylalkylglycerol modified with a long-chain cyclic acetal at the sugar moiety, 3-O-(4′6′-plasmalogalactosyl) 1-O-alkylglycerol, was isolated from equine brain. The presence of cyclic acetal linkage, its linked position, and the len
Externí odkaz:
https://doaj.org/article/75214ea2c4714f8f81cf90515bb0e0ff
Autor:
Youichi Yachida, Motoi Kashiwagi, Takeshi Mikami, Keiko Tsuchihashi, Takumi Daino, Toyoaki Akino, Shinsei Gasa
Publikováno v:
Journal of Lipid Research, Vol 39, Iss 5, Pp 1039-1045 (1998)
Modified galactosylceramide with a long-chain cyclic acetal at the sugar moiety, plasmalogalactosylceramide, was isolated from equine brain. To identify the isomeric stereostructure of the natural product, the plasmalo derivative was chemically synth
Externí odkaz:
https://doaj.org/article/63d162bb546b49e89b47d88e2166c048
Autor:
Motoi Kashiwagi, Shinsei Gasa, Keiko Tsuchihashi, Youichi Yachida, Toyoaki Akino, Takumi Daino
Publikováno v:
Glycoconjugate Journal. 16:39-43
To elucidate the effect of a modification of ceramide on antigenicity of the carbohydrate of ganglioside, the reactivity of O-acetyl GM3 having 3-O-acetyl ceramide, which has been characterized as a gliomarelated ganglioside, with monoclonal antibody
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c4f0428b736893851eb92cafe5ee523
https://doi.org/10.1023/a:1006949719565
https://doi.org/10.1023/a:1006949719565
Autor:
Keiko Tsuchihashi, Toyoaki Akino, Takeshi Mikami, Motoi Kashiwagi, Takumi Daino, Shinsei Gasa, Youichi Yachida
Publikováno v:
Journal of Chromatography A. 813:325-332
To determine O-esterified positions, a rapid and complete acetalization to prepare an intermediate was established using ethyl vinyl ether as a new reagent. The new method was applied to O-esterified glycolipids followed by GC-MS analysis of the mono
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6f5171658e69104dae41d8907d06090
https://doi.org/10.1016/s0021-9673(98)00348-3
https://doi.org/10.1016/s0021-9673(98)00348-3
Autor:
Toyoaki Akino, Motoi Kashiwagi, Shinsei Gasa, Takumi Daino, Kazuo Hashi, Keiko Tsuchihashi, Youichi Yachida, Takeshi Mikami
Publikováno v:
European Journal of Biochemistry. 255:289-295
A sulfatide, O-fatty-acylated 3-sulfogalactosylceramide at C6-O on galactoside, was isolated from equine brain and the chemical structure was characterized by proton NMR and MS. The O-acylation site of the acylated sulfatide was determined by the dow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e90b46b39dd1e215daace479f61aa8ca
https://doi.org/10.1046/j.1432-1327.1998.2550289.x
https://doi.org/10.1046/j.1432-1327.1998.2550289.x
Autor:
Motoi Kashiwagi, Shinsei Gasa, Keiko Tsuchihashi, Toyoaki Akino, Takumi Daino, Takeshi Mikami
Publikováno v:
Journal of Biochemistry. 123:487-491
Equine brain gangliosides were isolated and their structures were characterized, to examine whether equine brain has N-glycolyl neuraminic acid in gangliosides, since other mammals predominantly possess N-acetyl neuraminic acid in brain gangliosides,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24a0a60b16b2528af628344eddf7ede9
https://doi.org/10.1093/oxfordjournals.jbchem.a021962
https://doi.org/10.1093/oxfordjournals.jbchem.a021962
Publikováno v:
Journal of Lipid Research, Vol 37, Iss 10, Pp 2136-2144 (1996)
An O-acetyl group was selectively introduced into the ceramide moiety at the C-3-O on ganglioside GM3 containing N-acetyl neuraminic acid, the product of which has been previously found in rat glioma tissue as a glioma-associated ganglioside. The int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a71703137bf0a7d36d2485b51011625
https://doi.org/10.1016/s0022-2275(20)37296-5
https://doi.org/10.1016/s0022-2275(20)37296-5
Autor:
Keiko Tsuchihashi, Toyoaki Akino, Motoi Kashiwagi, Takumi Daino, Shinsei Gasa, Takeshi Mikami, Youichi Yachida
Publikováno v:
Journal of Lipid Research, Vol 39, Iss 5, Pp 1039-1045 (1998)
Modified galactosylceramide with a long-chain cyclic acetal at the sugar moiety, plasmalogalactosylceramide, was isolated from equine brain. To identify the isomeric stereostructure of the natural product, the plasmalo derivative was chemically synth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43580369dc83abc2acd84c7a4a625f03
https://pubmed.ncbi.nlm.nih.gov/9610771
https://pubmed.ncbi.nlm.nih.gov/9610771