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Bioactive Isoquinoline Alkaloids with Diverse Skeletons from Fissistigma polyanthum.
Jiang, Kun; Liu, Xiao; Liu, Yu-Ming; Wang, Li-Ning; Xiao, Ya-Ting; Wu, Feng-Chen.
Affiliation
  • Jiang K; School of Chemistry and Chemical Engineering, Tianjin University of Technology, Tianjin 300384, People's Republic of China.
  • Liu X; School of Chemistry and Chemical Engineering, Tianjin University of Technology, Tianjin 300384, People's Republic of China.
  • Liu YM; School of Chemistry and Chemical Engineering, Tianjin University of Technology, Tianjin 300384, People's Republic of China.
  • Wang LN; College of Traditional Chinese Medicine, Tianjin Univerisity of Traditional Chinese Medicine, Tianjin 300193, People's Republic of China.
  • Xiao YT; School of Chemistry and Chemical Engineering, Tianjin University of Technology, Tianjin 300384, People's Republic of China.
  • Wu FC; School of Chemistry and Chemical Engineering, Tianjin University of Technology, Tianjin 300384, People's Republic of China.
J Nat Prod ; 86(9): 2162-2170, 2023 09 22.
Article in En | MEDLINE | ID: mdl-37615114
ABSTRACT
Six new isoquinoline alkaloids, including aporphine alkaloids (2, 3, 9, and 10), a benzylisoquinoline alkaloid (13), and a protoberberine alkaloid (17), were isolated from the roots of Fissistigma polyanthum, along with a new furanone (20) and 13 known isoquinoline alkaloids (1, 4-8, 11, 12, 14-16, 18, and 19). The structures of the new compounds were elucidated by the analysis of spectroscopic data. Compounds 1 and 2 are rare oxalyl-fused dehydroaporphine alkaloids. Compound 12 presented the most potent dual-target activities on AChE inhibition and Aß aggregation inhibition, while compounds 13 and 19 simultaneously exhibited discernible AChE and BChE inhibitions with antioxidant activities. The activity results indicate that F. polyanthum alkaloids have a potential of inhibition and prevention of Alzheimer's disease mainly through both ChEs and ß-amyloid pathways in addition to antioxidant activity.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Annonaceae / Benzylisoquinolines / Alkaloids Language: En Journal: J Nat Prod Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Annonaceae / Benzylisoquinolines / Alkaloids Language: En Journal: J Nat Prod Year: 2023 Document type: Article