Aconitum japonicum

Aconitum carmichaelii (Ranunculaceae) kjp 29,129 98 Aconitum japonicum (Ranunculaceae) jnp 44, 53 81 Aconitum koreanum (Ranunculaceae) kjp 29,129 98 Aconitum kusnezoffii (Ranunculaceae) kjp 29,129 98... [Pg.80]

Aconitum ibukiense Nakai 9-Hydroxynominine Ignavine Ryosenamine Ryosenaminol Aconitum japonicum Thunb. [Pg.38]

Aconitum japonicum var. montanum Nakai 3-ep/ -Ignavinol Kobusine... [Pg.38]

Nelumbo nudfera (Nelumbonaceae), Aconitum japonicum (Ranunculaceae)... [Pg.186]

Nelumbo nucifera Gaertn. and Aconitum Japonicum Decne. ... [Pg.28]

Demethylcoclaurine has been isolated from the seed embryos of Nelumbo nucifera Gaertn. and exhibits smooth muscle and uterine relaxation activity. Its racemate, called higenamine, is found in Aconitum japonicum Decne. The levorotatory form has shown much stronger cardiac activity in the frog s heart test than its enantiomer. ... [Pg.50]

Aconitum ibukiense Nakai1,. carmichaeli Debeaux2, A. japonicum Thunb.3,7, A. san-yoense Nakai4, A. species6... [Pg.258]

Aconitum yesoense var. macroyesoense (Na-kai)3 Tamura, A. japonicum Thumb, A. tal-assicumM. Pop6, A. japonicum var. monta-num Nakai5... [Pg.273]

Isohypognavine has been isolated (99, 106) from the roots of A. majijai Nakai and A. japonicum Thumb. Its name is unfortunate since it is not an isomer of hypognavine. This alkaloid has not been isolated from any other Aconitum species. On alkaline hydrolysis, isohypognavine gave an alkamine known as isohypognavinol. On the basis of chemical correlation (107) of isohypognavine with kobusine, the partial structures 108 and 109 were... [Pg.130]

Aconitum majimai, A. japonicum etc. Chemically correlated with kobusine Refs. 99, 106, 107... [Pg.202]

Mesaconitine was first isolated (103) in 1929 and occurs in a large number of Aconitum species (1). Recent reports describe its isolation from A. japonicum (104), A. mitakense (101), A. aUaicum Steinb. (105), and A. carmichalei (the Chinese drug Chuan-wu) (73). It has long been known that mesaconitine differs from aconitine only in that the former has an iV -methyl whereas the latter has an JV-ethyl (1). Both alkaloids produce oxonitine (CXXXIII) from permanganate oxidation. Hence, since the structure of aconitine has been established as CXXI, mesaconitine follows as CCV. [Pg.60]

Mesaconitine was first isolated in 1929 (29). This alkaloid occurs in a large number of Aconitum species reported in the earlier review (1). It has also been isolated from A. japonicum (29), A. mitakense (27), A. altaicum Steinb. (30), and the Chinese drug known as Chuan-Wu (14) ( . carmi-chalei). The structure of mesaconitine as 12 was based on the structure of aconitine. Because mesaconitine differs from aconitine only in possessing an JV-methyl instead of an N-ethyl group, the structure of mesaconitine must now be revised to 13. [Pg.7]

Aconitum napellus A. fauriei A. japonicum and others Correlated with aconitine Refs. 1, 3, 4, 20, 27, 28, 30... [Pg.95]

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