Synthesis of Novel C-2- or C-15-Labeled BODIPY-Estrone Conjugates

Molecules. 2018 Apr 3;23(4):821. doi: 10.3390/molecules23040821.

Abstract

Novel BODIPY-estrone conjugates were synthesized via Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC). Estrone-alkynes or an estrone-azide as starting compounds were synthesized via Michael addition or Sonogashira reaction as key steps. Fluorescent dyes based on BODIPY-core were provided by azide or alkyne functional groups. Fluorescent labeling of estrone was efficiently achieved at the C-2 or C-15 position. The newly-elaborated coupling procedures might have a broad applicability in the synthesis of fluorescent-labeled estrone conjugates suitable for biological assays.

Keywords: BODIPY; CuAAC; estrone; estrone conjugates; fluorescent labeling.

MeSH terms

  • Alkynes / chemical synthesis
  • Alkynes / chemistry
  • Azides / chemical synthesis
  • Azides / chemistry
  • Boron Compounds / chemistry*
  • Catalysis
  • Click Chemistry / methods
  • Estrone / chemistry*

Substances

  • 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
  • Alkynes
  • Azides
  • Boron Compounds
  • Estrone