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Flueggeacosines A-C, Dimeric Securinine-Type Alkaloid Analogues with Neuronal Differentiation Activity from Flueggea suffruticosa.

Zhen-Long WuXiao-Jun HuangMing-Tao XuXuanyue MaLiuren LiLei ShiWen-Jing WangRen-Wang JiangWen-Cai YeYing Wang
Published in: Organic letters (2018)
Flueggeacosines A-C (1-3), three dimeric securinine-type alkaloid analogues with unprecedented skeletons, were isolated from Flueggea suffruticosa. Compounds 1 and 2 are the first examples of C-3-C-15' connected dimeric securinine-type alkaloids. Compound 3 is an unprecedented heterodimer of securinine-type and benzoquinolizidine alkaloids. Biosynthetic pathways for 1-3 were proposed on the basis of the coexisting alkaloid monomers as the precursors. Compound 2 exhibited significant activity in promoting neuronal differentiation of Neuro-2a cells.
Keyphrases
  • molecular docking
  • signaling pathway
  • cell proliferation
  • cell death
  • blood brain barrier
  • molecular dynamics simulations