Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Fumiko Nishida"'
Publikováno v:
Biochemical and Biophysical Research Communications. 283:976-981
The world's oceans are iron-deficient environments and there is little knowledge available regarding iron uptake by marine sponges. To understand iron-related biofunctions in marine organisms, iron-binding natural compounds from marine sponges were i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb057068034f15bdfda26204800372d1
https://doi.org/10.1006/bbrc.2001.4890
https://doi.org/10.1006/bbrc.2001.4890
Autor:
Kenji Nabeshima, Rie Takagi, Shiho Hirohara, Akihisa Hamazawa, Masanori Morita, Tomoaki Tanase, Maki Tanahashi, Katsuki Takashiba, Yuka Nakamura, Kaoru Mogami, Tadashi Okamoto, Mika Yokoyama, Izabela Brudziñska, Fumiko Nishida, Kimiko Esaki, Masahiko Takatani, Shigenobu Yano, Yuji Mikata, Kazumi Yoneda, Chris Orvig, Yoshie Shinohara, Matsumi Doe, Takashi Kitayama, Toru Sakakibara, Isamu Kinoshita
Publikováno v:
The Journal of Organic Chemistry. 66:3783-3789
A set of 1,3-propanediamine derivatives connected to carbohydrates (5) has been prepared in four steps from peracetylated sugar and 1,3-dibromo-2-propanol in 60-73% yields. D-Glucose, D-mannose, D-galactose, D-xylose, D-ribose, and maltose are utiliz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::691b5cea5767044e9cecafe4252d0ef2
https://doi.org/10.1021/jo001702+
https://doi.org/10.1021/jo001702+
Autor:
Masami Kobayashi, Machiko Akiyama, Nobuaki Ishida, Hideo Kise, Hiromi Kano, Mika Koizumi, Hirozo Oh-oka, Tadashi Watanabe, Jan Amesz, Satoshi Akutsu, Fumiko Nishida, Keisuke Tominaga
Publikováno v:
Photosynthesis Research. 63:269-280
The primary electron acceptor of green sulfur bacteria, bacteriochlorophyll (BChl) 663, was isolated at high purity by an improved purification procedure from a crude reaction center complex, and the molecular structure was determined by fast atom bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6d3bf0ffe0e13386f8e97cf554ad9cf
https://doi.org/10.1023/a:1006480629059
https://doi.org/10.1023/a:1006480629059
Autor:
Fumiko Nishida, Miyuki Nishijima, Tadashi Maruyama, Hiroshi Sano, Yoshihiko Sako, Norimichi Nomura, Kenichi Mochida
Publikováno v:
FEMS Microbiology Letters. 174:339-346
Aeropyrum pernix is the first strictly aerobic hyperthermophile known to grow heterotrophically at neutral pH and at temperatures up to 100°C. Using a simple and sensitive frit-fast atom bombardment liquid chromatography/mass spectrometry quinone an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::643ec231768657a1471d0dc3199313dd
https://doi.org/10.1111/j.1574-6968.1999.tb13588.x
https://doi.org/10.1111/j.1574-6968.1999.tb13588.x
Autor:
Isamu Kinoshita, Fumiko Nishida, Kazumi Yoneda, Yuji Mikata, Matsumi Doe, Shigenobu Yano, Kenichi Mochida, Tomoaki Tanase
Publikováno v:
Carbohydrate Research. 313:175-179
A useful preparation of an ethylenediamine derivative linked to d- glucose, 2,3-diaminopropyl β- d- glucopyranoside, has been described. The optically pure compound was obtained conveniently via recrystallization of the diastereomeric mixture of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bac3937490dd6b2b3b254d8140e5943b
https://doi.org/10.1016/s0008-6215(98)00268-7
https://doi.org/10.1016/s0008-6215(98)00268-7
Autor:
Tsuyoshi Fujita, Hideo Naoki, Suthum Intararuangsorn, Ken-ichi Harada, Vithaya Meevootisom, Timothy W. Flegel, Makoto Suzuki, Yodohathai Thebtaranonth, Fumiko Nishida
Publikováno v:
Journal of the Mass Spectrometry Society of Japan. 43:37-44
The exact positions of the acetyl groups in the sugar moieties of the glycosidic antibiotics, the glykenin (GK) components, were elucidated using MS/MS technique under high energy collision conditions, because the frit-FAB LC/MS technique that was de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::178bf909acc6405b7fbb9c62ab2da971
https://doi.org/10.5702/massspec.43.37
https://doi.org/10.5702/massspec.43.37
Autor:
Matsumi Doe, Yuji Mikata, Kazumi Yoneda, Fumiko Nishida, Isamu Kinoshita, Tomoaki Tanase, Kenichi Mochida, Shigenobu Yano
Publikováno v:
ChemInform. 30
A useful preparation of an ethylenediamine derivative linked to d- glucose, 2,3-diaminopropyl β- d- glucopyranoside, has been described. The optically pure compound was obtained conveniently via recrystallization of the diastereomeric mixture of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ca1f986193599b367053922ed5d1092
https://doi.org/10.1002/chin.199931236
https://doi.org/10.1002/chin.199931236
Autor:
Makoto Suzuki, Yuji Mori, Vithaya Meevootisom, Fumiko Nishida, Suthum Intararuangsorn, Timothy W. Flegel, Yodhathai Thebtaranonth
Publikováno v:
Chemical and Pharmaceutical Bulletin. 39:3044-3047
Three new glycosidic antibiotics, glykenin (GK)-III A, B, and C (2a-c), were isolated as a mixture from a strain of Basidiomycetes sp. and identified as glycosides of C26-fatty acids and a diacetylated trisaccharide composed of glucose and two xylose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81c4a1fcec910ca9fb74501bc1a05ad4
https://doi.org/10.1248/cpb.39.3044
https://doi.org/10.1248/cpb.39.3044
Autor:
Chiharu Sonobe, Suthum Intararuangsorn, Timothy W. Flegel, Yuji Mori, Vithaya Meevootisom, Yodhathai Thebtaranonth, Fumiko Nishida, Makoto Suzuki
Publikováno v:
The Journal of Antibiotics. 44:541-545
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa83bf6caf8da194da1cb4c6a2c06445
https://doi.org/10.7164/antibiotics.44.541
https://doi.org/10.7164/antibiotics.44.541
Autor:
Yuji Mori, Vithaya Meevootisom, Sayuri Isobe, Suthum Intararuangsorn, Timothy W. Flegel, Makoto Suzuki, Yodhathai Thebtaranonth, Takeyuki Furuse, Naoko Rokkaku, Fumiko Nishida
Publikováno v:
Chemical and Pharmaceutical Bulletin. 38:2381-2389
The structures of three aglycones of glykenins, produced by Basidiomycetes sp., were determined to be (2S, 16R, 17S, 21R)-2, 16, 17, 21-, (2S, 17R, 18S, 22R)-2, 17, 18, 22-, and (2S, 17S, 18S, 22R)-2, 17, 18, 22-tetrahydroxyhexacosanoic acids (3a-c).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff2fd79af8e299b8f2bcd52a71cde1b3
https://doi.org/10.1248/cpb.38.2381
https://doi.org/10.1248/cpb.38.2381