(1S,8aα)-6β-アミノオクタヒドロインドリジン-1β-オールアセタート

(1S,8aα)-6β-アミノオクタヒドロインドリジン-1β-オールアセタート 化学特性,用途語,生産方法

• 説明

  Certain legume forages used for dairy cattle feeding stock have been known to produce excessive salivation when infested by Rhizoctonia legurninicola and this has been shown to be due to the presence of an indolizidine alkaloid, slaframine. The base is amorphous and also yields an amorphous dihydrochloride. The dipicrate, however, is crystalline, m.p. l83-4°C as is also the N-acetyl derivative, m.p. l43-6°C; [α]²⁵_D - 15.9° (c 5.0, EtOH). NMR and high-resolution mass spectrometry have shown that the earlier structure required revision to that given above, namely l-acetoxy-6-aminooctahydroindolizidine. The configuration has been demonstrated to be 1 S,6S,8aS-.

• 使用

  (-)-Slaframine, is an indolizidine alkaloidal mycotoxin that generally causes salivation (slobbers) in most animals. It is usually produced by the fungus Rhizoctonia leguminicola.

• 定義

  ChEBI: An indolizidine alkaloid that is octahydroindolizine substituted by an amino group at position 6 and an acetyloxy group at position 1.

• 参考文献

  Rainey et al., Nature, 205, 203 (1965)
  Aust, Broquist., ibid, 205, 204 (1965)
  Aust, Broquist, Rinehart.,l. Arner. Chern. Soc., 88,2879 (1966)
  Whitlock et al., Tetrahedron Lett., 3819 (1966)
  Revised structure:
  Gardiner et al., J. Arner. Chern. Soc., 90,5639 (1968)

(1S,8aα)-6β-アミノオクタヒドロインドリジン-1β-オールアセタート 生産企業

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