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Three Novel Biphenanthrene Derivatives and a New Phenylpropanoid Ester from Aerides multiflora and Their α-Glucosidase Inhibitory Activity.

May Thazin ThantBoonchoo SritularakNutputsorn ChatsumpunWanwimon MekboonsonglarpYanyong PunpreukKittisak Likhitwitayawuid
Published in: Plants (Basel, Switzerland) (2021)
A phytochemical investigation on the whole plants of Aerides multiflora revealed the presence of three new biphenanthrene derivatives named aerimultins A-C (1-3) and a new natural phenylpropanoid ester dihydrosinapyl dihydroferulate (4), together with six known compounds (5-10). The structures of the new compounds were elucidated by analysis of their spectroscopic data. All of the isolates were evaluated for their α-glucosidase inhibitory activity. Aerimultin C (3) showed the most potent activity. The other compounds, except for compound 4, also exhibited stronger activity than the positive control acarbose. Compound 3 showed non-competitive inhibition of the enzyme as determined from a Lineweaver-Burk plot. This study is the first phytochemical and biological investigation of A. multiflora.
Keyphrases
  • molecular docking
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  • high resolution
  • structure activity relationship
  • single cell
  • deep learning
  • data analysis