Dimeric pyrrolidinoindoline-type alkaloids with melanogenesis inhibitory activity in flower buds of Chimonanthus praecox

J Nat Med. 2014 Jul;68(3):539-49. doi: 10.1007/s11418-014-0832-1. Epub 2014 Mar 26.

Abstract

A methanol extract of the flower buds of Chimonanthus praecox (L.) Link (Calycanthaceae) demonstrated inhibitory effects on melanogenesis in theophylline-stimulated murine B16 melanoma 4A5 cells. From the extract, five dimeric pyrrolidinoindoline alkaloids and four sesquiterpenes were isolated, together with 16 known compounds. Among them, (-)-chimonanthine (1, IC50 = 0.93 μM), (-)-folicanthine (2, 1.4 μM), and (-)-calycanthidine (3, 1.8 μM) showed potent inhibitory effects without notable cytotoxicity at the effective concentrations. The most potent alkaloid (1) inhibited both tyrosinase and tyrosine-related protein-1 mRNA expressions, to which the melanogenesis inhibitory activity would be ascribable.

MeSH terms

  • Alkaloids / chemistry
  • Alkaloids / pharmacology*
  • Animals
  • Calycanthaceae / chemistry*
  • Cell Line, Tumor
  • Dimerization
  • Flowers / chemistry
  • Indoles / chemistry
  • Indoles / pharmacology*
  • Melanins / biosynthesis*
  • Mice
  • Monophenol Monooxygenase / metabolism
  • Pyrroles / chemistry
  • Pyrroles / pharmacology*
  • Sesquiterpenes / chemistry
  • Sesquiterpenes / pharmacology

Substances

  • Alkaloids
  • Indoles
  • Melanins
  • Pyrroles
  • Sesquiterpenes
  • Monophenol Monooxygenase