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Yunaconitine

Ludaconitine Gigactonine Yunaconitine Heterophylloidine (panicutine) Ryosenaminol Ibukinamine Ryosenamine C2 0H2 7NO2 A1 jesaconitine A A1 jesaconitine B Sadosine... [Pg.376]

Alkaloids of Aconitum hemsleyanum Yunaconitine.—Research carried out in the Peoples Republic of China has resulted in the isolation of a new alkaloid from A. hemsleyanum Pritz. var. circinatum W. T. Wang and from A. geniculatum Flet. et Laue. var. unguiculatum W. T. Wang. The structure of yunaconitine (19) [C3sH49NO m. pt. 141—143 C (perchlorate m. pt. 226—230 nitrate m. [Pg.214]

More recent studies on new Aconitum alkaloids allowed to identify a range of molecules possessing analgesic activity on different pain models [34—36]. Among them, four alkaloids, bulleyaconitine, (V-deacetyllappacOTiitine, yunaconitine, and... [Pg.1509]

The first group consists of the most toxic alkaloids such as aconitine, mesaconitine, hypaconitine, 3-acetylaconitine, jesaconitine, yunaconitine, beiwutine, buUeyaconitine, etc. Their molecular strucmres are relatively similar (12, Table 48.6). The common feature of all these alkaloids is the presence of two ester groups on position C-8 formed by acetyl moiety and on position C-14 formed by benzoyl or anisoyl moiety. [Pg.1517]

See other pages where Yunaconitine is mentioned: [Pg.93]    [Pg.672]    [Pg.264]    [Pg.264]    [Pg.286]    [Pg.288]    [Pg.214]    [Pg.214]    [Pg.1508]    [Pg.1509]    [Pg.1518]    [Pg.1519]    [Pg.1520]    [Pg.93]    [Pg.672]    [Pg.264]    [Pg.264]    [Pg.286]    [Pg.288]    [Pg.214]    [Pg.214]    [Pg.1508]    [Pg.1509]    [Pg.1518]    [Pg.1519]    [Pg.1520]   
See also in sourсe #XX -- [ Pg.376 ]



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