[A new cinnamic acid ester derivative from Liquidambaris Resina]

Zhongguo Zhong Yao Za Zhi. 2023 Aug;48(15):4130-4136. doi: 10.19540/j.cnki.cjcmm.20230426.201.
[Article in Chinese]

Abstract

Twelve compounds were isolated from Liquidambaris Resina by silica gel column chromatography and thin layer chromatography. Their structures were identified on the basis of spectral data, electron capture detector data, and physicochemical properties as(2'R, 3'R)-2',3'-dihydroxy-hydrocinnamyl-(E)-cinnamate(1),(E)-cinnamyl-(E)-cinnamate(2), cinnamic acid(3), 28-norlup-20(29)-en-3-one-17β-hydroperoxide(4), erythrodiol(5), 13β,28-epoxy-30-hydroxyolean-1-en-3-one(6),(3β)-olean-12-ene-3,23-diol(7), 2α,3α-dihydroxy-olean-12-en-28-oic acid(8), 28-hydroxyolean-12-en-3-one(9), 3-epi-oleanolic acid(10), 3-oxo-oleanolic acid(11), and hederagenin(12). Compound 1 was a new cinnamic acid ester derivative and compounds 2-4,6-8, and 12 were isolated from Liquidambaris Resina for the first time. Compounds 4, 5, 10, and 12 exerted inhibitory effects on the proliferation of human umbilical vein endothelial cells(HUVEC) with the IC_(50) values of(17.43±2.17),(35.32±0.61),(27.50±0.80), and(46.30±0.30) μmol·L~(-1), respectively.

Keywords: Liquidambar formosana; Liquidambaris Resina; chemical constituents; cinnamic acid ester.

Publication types

  • English Abstract

MeSH terms

  • Cinnamates
  • Endothelial Cells
  • Esters
  • Humans
  • Molecular Structure
  • Oleanolic Acid*
  • Triterpenes* / chemistry

Substances

  • Oleanolic Acid
  • cinnamic acid
  • Esters
  • Cinnamates
  • Triterpenes