LSD1 inhibitors from the roots of Pueraria lobata

J Asian Nat Prod Res. 2023 Jan;25(1):44-52. doi: 10.1080/10286020.2022.2032677. Epub 2022 Feb 3.

Abstract

One new 6a,11a-dehydropterocarpan derivative, 6-O-methyl-anhydrotuberosin (1), one new 6a-hydroxypterocarpan, (6aR,11aR,11bR)-hydroxytuberosone (7), and seven known compounds including two 6a,11a-dehydropterocarpans (2 and 4), two coumestans (3 and 5), one isoflavonoid (6) and two other phenolic compounds (8 and 9) were isolated from the roots of Pueraria lobata. The structures of the isolated compounds were elucidated with spectroscopic and spectrometric methods (1 D and 2DNMR, HRESIMS). Compounds 1, 2, 4-5 showed potent LSD1 inhibitory activities with IC50 values ranging from 1.73 to 4.99 μM. Furthermore, compound 2 showed potent cytotoxicity against gastric cancer cell lines MGC-803 and BGC-823, and lung cancer cell lines H1299 and H460.

Keywords: LSD1 inhibitors; Pueraria lobata; isoflavonoid; pterocarpan.

MeSH terms

  • Cell Line
  • Histone Demethylases / analysis
  • Isoflavones* / chemistry
  • Isoflavones* / pharmacology
  • Phenols
  • Plant Roots / chemistry
  • Pueraria* / chemistry

Substances

  • Phenols
  • Histone Demethylases
  • Isoflavones