Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Hideo Bando"'
Autor:
Hiroshi Yamashita, Takahisa Nakane, Koji Wada, Hideo Bando, Kuo Hsiung Lee, Madoka Matsuzaki, Toshiro Shibata, Yuria Kurokawa, Masuo Goto
Publikováno v:
Phytochem Lett
Four novel lupane-type lupane-type triterpenoids (including three norlupane-type triterpenoids), 17β-hydroxy-28-norlup-20(29)-en-3-one (1), 3β,17β–dihydroxy-28,30-bisnorlupan-20-one (2), 3β-hydroxy-20-oxo-30-norlupan-28-al (3) and lup-20(29)-en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cdf275ac5e763c0bf48cc52a1f79522
https://doi.org/10.1016/j.phytol.2019.03.015
https://doi.org/10.1016/j.phytol.2019.03.015
Autor:
Shinji Nagumo, Hiroyuki Akita, Hideo Bando, Koji Wada, Toshie Miura, Masaaki Miyashita, Yasunori Hashimoto, Megumi Mizukami, Norio Kawahara
Publikováno v:
Tetrahedron Letters. 48:8558-8561
The TMSOTf-promoted Friedel–Crafts-type reaction of vinyloxirane 3 having a nitrogen atom at the benzylic position was found to proceed with a highly selective 7- endo mode to afford hydro-2-benzazepine 4 in high yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b81d40570f71b93224076aecb1fca182
https://doi.org/10.1016/j.tetlet.2007.09.106
https://doi.org/10.1016/j.tetlet.2007.09.106
Autor:
Takako Aoyama, Kumiko Shimozawa, Yukari Noguchi, Kouichi Jinbow, Hideo Bando, Kiyoshi Horita, Makoto Nishizawa, Nobuaki Takahashi, Takashi Yamagishi
Publikováno v:
Fisheries Science. 69:639-643
Four steroidal ketones were isolated from the holdfast of cultivated Laminaria japonica. The structures were characterized as ergosta-4,24(28)-diene-3-one (1), ergosta-4,24(28)-diene-3,6-dione (2), stigmasta-4,24(28)-diene-3-one (3) and stigmasta-4,2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9261b1d16d68227638b9b8ab1d7f8b70
https://doi.org/10.1046/j.1444-2906.2003.00667.x
https://doi.org/10.1046/j.1444-2906.2003.00667.x
Publikováno v:
Fisheries science. 65:909-913
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c27a033440fc85cacbe8f44e6d476f04
https://doi.org/10.2331/fishsci.65.909
https://doi.org/10.2331/fishsci.65.909
Publikováno v:
Biological and Pharmaceutical Bulletin. 20:978-982
Nine alkaloid constituents in the root of Aconitum yesoense var. macroyesoense, as well as three acetylated derivatives, were examined for their peripheral vaso-activities by measuring laser-flowmetrically the cutaneous blood flow in the hind foot of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c47d23cf6f88b3b087ae3d7bbbcd90bf
https://doi.org/10.1248/bpb.20.978
https://doi.org/10.1248/bpb.20.978
Publikováno v:
Biological Mass Spectrometry. 23:97-102
A high-performance liquid chromatography/atmospheric pressure chemical ionization mass spectrometric method was useful for the simultaneous determination of aconitine-type alkaloids (jesaconitine, aconitine, mesaconitine, aljesaconitine A, aljesaconi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9b6b26f8206b03e2652d972b44aebbc
https://doi.org/10.1002/bms.1200230209
https://doi.org/10.1002/bms.1200230209
Publikováno v:
Journal of Chromatography A. 644:43-48
A high-performance liquid chromatography—atmospheric pressure chemical ionization mass spectrometry method was useful for the simultaneous determination of Aconitum alkaloids, kobusine, pseudokobusine, dehydrolucidusculine, lucidusculine, delcosine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34da9ae6ecc930df7743be8d1507b30a
https://doi.org/10.1016/0021-9673(93)80118-r
https://doi.org/10.1016/0021-9673(93)80118-r
Publikováno v:
Phytochemistry. 31:2135-2138
Four new C 19 -diterpenoid alkaloids, pacifidine, pacifiline, pacifinine and pacidine, and five known alkaloids were isolated from Delphinium elatum cv. Pacific Giant. The structures of these alkaloids were determined on the basis of their spectral d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f197374915ce7e30be332585aad4bf7d
https://doi.org/10.1016/0031-9422(92)80380-w
https://doi.org/10.1016/0031-9422(92)80380-w
Autor:
Masashi Shinohara, Ryuichi Nishida, Makoto Nishizawa, Hideo Bando, Taizo Motomura, Masakazu Tatewaki
Publikováno v:
Phycological Research. 48:91-93
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ee2322ed0198dc17d14ff16011a1d3f
https://doi.org/10.1111/j.1440-1835.2000.tb00201.x
https://doi.org/10.1111/j.1440-1835.2000.tb00201.x
Publikováno v:
Chemical and Pharmaceutical Bulletin. 39:379-383
The role of the substituents at C3 and C8 of jesaconitine (1) on jesaconitine-induced analgesia and toxicity was examined. 3-O-Acetyljesaconitine (2), 3-O-anisoyljesaconitine (3), and 3-deoxyjesaconitine (6) showed dose-dependent analgesic action, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8540ca1f9dda598e22869ed92bf59b3d
https://doi.org/10.1248/cpb.39.379
https://doi.org/10.1248/cpb.39.379