Soluble epoxide hydrolase inhibitors from Docynia indica (Wall.) Decne

Nat Prod Res. 2021 Dec;35(23):5403-5408. doi: 10.1080/14786419.2020.1774759. Epub 2020 Jun 8.

Abstract

Nine bioactive compounds, including one new dihydroisocoumarin glycoside, 3S-thunberginol C 6-O-β-D-glucopyranoside (1a/1b), were isolated by chromatographic separation from the fruits of the Vietnamese medicinal plant Docynia indica (Wall.) Decne. 3S-thunberginol C 6-O-β-D-glucopyranoside was determined as a mixture of boat-like conformers based on NMR evidence and density functional theory (DFT) calculations. The in vitro inhibition of soluble epoxide hydrolase (sEH) by the isolated compounds was comparable to that of AUDA (positive control), yielding IC50 values ranging from 10.0 ± 0.6 to 88.4 ± 0.2 µM. Among isolated compounds, 3-methoxy-4-hydroxy-benzoic acid (7) and 2',6'-dihydroxy 3',4'-dimethoxychalcone (9) were identified as a potent inhibitor of sEH, with IC50 values of 19.3 ± 2.2 and 10.0 ± 0.6 mM, respectively. These results suggest that the fruits of D. indica may be useful as daily supplements for the prevention of cardiovascular and other sEH-related diseases.[Figure: see text].

Keywords: 3-aryl dihydroisocoumarin; 3S-thunberginol C 6-O-β-D-glucopyranoside; CD spectrum; DFT; Docynia indica; boat-like conformer; soluble epoxide hydrolase.

MeSH terms

  • Enzyme Inhibitors
  • Epoxide Hydrolases*
  • Fruit
  • Glycosides*

Substances

  • Enzyme Inhibitors
  • Glycosides
  • Epoxide Hydrolases