Caryopincaolide M, a rearranged abietane diterpenoid with new skeleton and a new iridoid from Caryopteris incana

J Nat Med. 2019 Jan;73(1):210-216. doi: 10.1007/s11418-018-1268-9. Epub 2018 Nov 24.

Abstract

Caryopincaolide M (1), a new rearranged abietane diterpenoid with an unusual pent-4-enoic acid group on a 6/6/5 tricyclic ring system, and 7-epi-8-dehydroxypatriscabrol (3), a new iridoid, together with 17 known compounds, have been isolated from the whole plant of Caryopteris incana (Thunb.) Miq. Their structures were elucidated on the basis of 1-D and 2-D NMR, IR, and mass spectroscopic data. Compounds 1-5 were evaluated for their inhibitory activities against enzyme α-glucosidase, and the results showed that only 1 has moderate inhibitory activity against enzyme α-glucosidase with IC50 at 528.3 ± 12.37 mg/L.

Keywords: Caryopteris incana; Diterpenoid; Iridoid; α-glucosidase.

MeSH terms

  • Abietanes / chemistry*
  • Molecular Structure
  • Plant Extracts / chemistry*

Substances

  • Abietanes
  • Plant Extracts