Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Haruji Oshio"'
Publikováno v:
YAKUGAKU ZASSHI. 96:855-862
Autor:
Hiroyuki Inouye, Haruji Oshio
Publikováno v:
Phytochemistry. 21:133-138
From the roots of Rehmannia glutinosa var. purpurea and R. glutinosa var. hueichingensis, besides four known iridoid glucosides, catalp
Autor:
Masae Yamaki, Miho Okihara, Kazuo Yamasaki, Osamu Tanaka, Ryoji Kasai, Haruji Oshio, Itsuo Nishioka, Yayoi Masaki, Masahiko Tsuboi, Shuzo Takagi, Gen-ichiro Nonaka, Kyoko Masuda
Publikováno v:
Tetrahedron Letters. 18:1231-1234
Publikováno v:
Chemical and Pharmaceutical Bulletin. 26:2458-2464
A study on the estimation of sennosides and derivatives of oxyanthraquinones in rhubarb and senna is described. After extracing a ground crude drug with the mixture of calcium acetate buffer and tetrahydrofuran (THF), the extract was fractionated to
Publikováno v:
Phytochemistry. 27:3585-3591
Ten minor saponins, momordins Ia–Ie and IIa–IIe, were isolated from the root of Momordica cochinchinensis , along with the known major saponins, momordins I and II. Their structures were established on the basis of chemical and spectroscopic anal
Publikováno v:
Chemical and Pharmaceutical Bulletin. 37:135-139
6"-Malonylginsenosides-Rb1, (6), -Rd (7) and 6"-malonylgypenoside V (8) were isolated from the fresh leaves of Gynostemma pentaphyllum selected from wild plants. It was found that the saponin content of dry leaves was markedly reduced because of deco
Publikováno v:
Chemical and Pharmaceutical Bulletin. 22:823-831
Besides sennoside A, sennosides B, C, E and F were isolated from rhubarbs. Sennosides E and F are new compounds and have comparable purgative activity to other sennosides. Sennosides E and F are stereoisomer mutually, and they are oxalates of sennosi
Autor:
Hiroshi Morimoto, Haruji Oshio
Publikováno v:
Justus Liebigs Annalen der Chemie. 682:212-218
Aus den Blattern von Lespedeza bicolor var. japonica wurde, neben geringen Mengen von Nω.Nω-Dimethyl-tryptamin (I), ein neues Alkaloid, C13H18N2O, Sdp.0.28 113–114°, gewonnen. Es zeigt eine positive Ehrlich-Reaktion, im NMR-Spektrum eine Methoxy
Publikováno v:
YAKUGAKU ZASSHI. 95:484-486
Autor:
Hiroshi Morimoto, Haruji Oshio
Publikováno v:
Justus Liebigs Annalen der Chemie. 676:168-170
Bei der Umsetzung von 7-Methoxy-indol mit Oxalylchlorid und anschliesend mit Dimethylamin wird [7-Methoxy-indolyl-(3)]-glyoxylsauredimethylamid (IV) erhalten. Es wurde durch Reduktion mit LiAlH4 in 7-Methoxy-Nω.Nω-dimethyl-tryptamin (V) ubergefuhrt