Iridoids and sfingolipids from Hedyotis diffusa

Fitoterapia. 2018 Jan:124:152-159. doi: 10.1016/j.fitote.2017.11.004. Epub 2017 Nov 6.

Abstract

Seven new compounds were isolated from the aerial part of Hedyotis diffusa, including three iridoid glycosides, hedyoiridoidside A - C (1-3), two cerebrosides, hedyocerenoside F (4) and G (5), and two new ceramides, hedyoceramide A (6) and B (7). And six known iridoid glycosides (8-13) were also obtained. Their structures were established by their physico-chemical constants and spectroscopic analysis. The cytotoxicity of all compounds against tumor cell lines of human cervical cancer HeLa, human leukemia HL-60, human lung cancer A459, human hepatoma HepG2, human gastric gland carcinoma BCG-823, human nasopharyngeal cancer CNE-2, human colon cancer HCT15, and human prostate cancer PC-3 were also evaluated in vitro. As a result, new compound 1 exhibited evident cytotoxicity to all tumor cell lines, and the IC50 values are from 9.5μM to 28.2μM, while new compound 2 exhibited evident cytotoxicity to Hela, HL-60, A459, HepG2, BGC-823, CNE-2, and HCT15, and the IC50 values are from 15.8μM to 26.2μM. Known compound 11 also exhibited evident cytotoxicity to HL-60, A459, HepG2, BGC-823, CNE-2, and HCT15, and the IC50 values are from 16.5μM to 40.4μM. New compounds 4-7 and known compounds 12 and 13 showed moderate cytotoxicity to some tumor cell lines.

Keywords: Asperuloside (PubChem CID: 84298); Asperulosidic acid (PubChem CID: 44423083); Ceramides; Cerebrosides; Cytotoxicity; Geniposidic acid (PubChem CID: 443354); Hedyotis diffusa; Iridoid glycosides; Scandoside (PubChem CID: 21602023).

MeSH terms

  • Antineoplastic Agents, Phytogenic / isolation & purification*
  • Cell Line, Tumor
  • Hedyotis / chemistry*
  • Humans
  • Iridoid Glycosides / isolation & purification*
  • Molecular Structure
  • Plant Components, Aerial / chemistry
  • Sphingolipids / isolation & purification*

Substances

  • Antineoplastic Agents, Phytogenic
  • Iridoid Glycosides
  • Sphingolipids