Affiliations 

  • 1 Faculty of Science and Marine Environment, Universiti Malaysia Terengganu, Terengganu, Malaysia
  • 2 Natural Products and Synthesis Organic Laboratory (NPSOLab), School of Chemical Science, Universiti Sains Malaysia, Minden, Pulau Pinang, Malaysia
  • 3 Bioprocess Technology Division, School of Industrial Technology, Universiti Sains Malaysia, Minden, Pulau Pinang, Malaysia
  • 4 Biological Security and Sustainability (BIOSES) Research Group, Faculty of Science and Marine Environment, Universiti Malaysia Terengganu, Terengganu, Malaysia
  • 5 Atta-ur-Rahman Institute for Natural Product Discovery, UiTM Cawangan Selangor, Bandar Puncak Alam, Selangor, Malaysia
  • 6 Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur, Malaysia
Nat Prod Res, 2023 Nov 27.
PMID: 38009213 DOI: 10.1080/14786419.2023.2283759

Abstract

Phytochemical investigation on the bark of E. kingiana plant afforded ten compounds, including six polyketides namely kingianin A 1, kingianin B 2, kingianin E 3, kingianin F 4, kingianin K 5 and kingianin L 6, three endiandric acids; kingianic acid A 7, tsangibeilin B 8 and endiandric acid M 9, and one sesquiterpene; daibuoxide 10. All compounds were separated as racemic mixture by recycling high-performance liquid chromatography (RHPLC), except for daibuoxide. Their structures were elucidated by detailed spectroscopic and comparative literature data analysis. This is the first report on the presence of the sesquiterpene; daibuoxide in Endiandra genus. In vitro enzymatic bio-evaluation of the isolated compounds against α-amylase and α-glucosidase showed that 4 demonstrated the best α-amylase and α-glucosidase inhibitory activity with IC50 values of 181.54 ± 6.27 µg/mL and 237.87 ± 0.07 µg/mL, respectively. In addition, molecular docking analysis confirmed the α-amylase and α-glucosidase inhibitory activities demonstrated by 4.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.