Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Kazuaki KYOGOKU"'
Publikováno v:
YAKUGAKU ZASSHI. 102:1041-1045
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac77021a18a8c46ee6b6bd082b187bca
https://doi.org/10.1248/yakushi1947.102.11_1041
https://doi.org/10.1248/yakushi1947.102.11_1041
Publikováno v:
YAKUGAKU ZASSHI. 102:659-665
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e19f89725ee7f03aaa82c2949ecc4d84
https://doi.org/10.1248/yakushi1947.102.7_659
https://doi.org/10.1248/yakushi1947.102.7_659
Publikováno v:
Agricultural and Biological Chemistry. 39:667-672
Sophoradin (I) [2′,4,4′-trihydroxy-3,3′,5-tris(3-methyl-2-butenyl)chalcone] which had been isolated from “Guang-Dou-Gen” (the root of Sophora subprostrata Chun et T. Chen) was synthesized through Claisen rearrangement. The reaction of p-hyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a6c022b91c19421ce1c070117d1cee9
https://doi.org/10.1271/bbb1961.39.667
https://doi.org/10.1271/bbb1961.39.667
Publikováno v:
Agricultural and Biological Chemistry. 39:133-138
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66f08ce4ae50010f578daa3af3e11c31
https://doi.org/10.1080/00021369.1975.10861552
https://doi.org/10.1080/00021369.1975.10861552
Publikováno v:
Japanese Journal of Pharmacology. 34:89-94
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff98d5acb1f6d25a9880a3fa787830c0
https://doi.org/10.1016/s0021-5198(19)52375-7
https://doi.org/10.1016/s0021-5198(19)52375-7
Publikováno v:
Agricultural and Biological Chemistry. 39:667-672
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e01697fd78c27604e540508f86395ecd
https://doi.org/10.1080/00021369.1975.10861645
https://doi.org/10.1080/00021369.1975.10861645
Autor:
Michitada Sasajima, Ryuichi Saziki, Ichiro Tanaka, Sadao Nakane, Katsuo Hatayama, Hideo Saotome, Kazuaki Kyogoku
Publikováno v:
Folia Pharmacologica Japonica. 74:897-905
A series of extracted fractions from sophora subprostrata was screened by determining anti-ulcer effects in pylorus ligated and stressed rats. Fr. [C-2] had the most potent anti-ulcer effects of all fractions extracted. Sophoradin and sophoranone whi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7595f82b41b72dd6a8b0f18d207a4c44
https://doi.org/10.1254/fpj.74.897
https://doi.org/10.1254/fpj.74.897
Publikováno v:
Agricultural and Biological Chemistry. 39:133-138
Sophoradin (I) [2′,4,4′-trihydroxy-3,3′,5-tris(3-methyl-2-buteny)chalcone] was synthesized through Claisen-Schmidt condensation followed by demethoxymethylation.Isoprenylation of p-hydroxybenzaldehyde with 3,3-dimethylallyl bromide in 10% potas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29a2defb4f1f8a0178ffc6bb364d5a88
https://doi.org/10.1271/bbb1961.39.133
https://doi.org/10.1271/bbb1961.39.133
Autor:
Yasuo Tarumoto, Susumu Otomo, Katsuharu Tsuchida, Masahiro Ohzeki, Kimiyo Takeshita, Shiro Nakaike, Makoto Tanaka, Kazuaki Kyogoku, Shohei Higuchi, Yoshiya Gotoh, Michitada Sasajima, Osada Y, Kenji Inoue
Publikováno v:
Folia Pharmacologica Japonica. 78:647-658
The topical and systemic anti-inflammatory activities of hydrocortisone 17-butyrate 21-propionate (HBP) were studied. The systemic anti-inflammatory activities of HBP and reference steroids were examined for their effects on dinitrochlorobenzene derm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09bfb1d03202ed4b7298b37d854c3f93
https://doi.org/10.1254/fpj.78.647
https://doi.org/10.1254/fpj.78.647
Autor:
Kazuaki Kyogoku, Kunihiro Suzuki, Manki Komatsu, Katsuo Hatayama, Kazuko Maejima, Sadakazu Yokomori
Publikováno v:
Chemical and Pharmaceutical Bulletin. 21:1777-1782
Two new flavanones were isolated from Guang-Dou-Gen (the root of Sophora subprostrata CHUN et T.CHEN) and their structures were established from their spectral data and comparison with the corresponding synthesized derivatives as 4', 7-dihydroxy-6, 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b80645f6c48a99969c0e0898635a376
https://doi.org/10.1248/cpb.21.1777
https://doi.org/10.1248/cpb.21.1777