Preparation, receptor binding, and fluorescence properties of hexestrol-fluorophore conjugates: evaluation of site of attachment, fluorophore structure, and fluorophore-ligand spacing

J Med Chem. 1987 Jan;30(1):156-65. doi: 10.1021/jm00384a026.

Abstract

We have undertaken a staged development of certain estrogen-fluorophore conjugates, in order to prepare a fluorescent estrogen suitable for determination of the estrogen receptor content of individual cells. Since non-steroidal estrogens with bulky substituents are often more readily bound by receptor than their steroidal counterparts, we have investigated fluorophore conjugates with derivatives of the non-steroidal estrogen hexestrol [3R*, 4S*)-3,4-bis(4-hydroxyphenyl)hexane). On the basis of the receptor-binding affinity of model compounds, we prepared a prototypical set of three ring- and side-chain-substituted fluorescent hexestrol derivatives, whose binding and fluorescence properties ultimately led to the preparation of a series of side-chain-substituted nitrobenzoxadiazole derivatives. The compounds prepared have binding affinities for the estrogen receptors that range from ca. 1% to 5% that of estradiol, and they have very favorable fluorescence characteristics, similar to those of fluorescein.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Estradiol / metabolism
  • Fluorescent Dyes / chemical synthesis*
  • Fluorescent Dyes / metabolism
  • Hexestrol / analogs & derivatives*
  • Hexestrol / chemical synthesis
  • Hexestrol / metabolism
  • Indicators and Reagents
  • Kinetics
  • Magnetic Resonance Spectroscopy
  • Mass Spectrometry
  • Receptors, Estrogen / metabolism*
  • Spectrophotometry, Infrared
  • Structure-Activity Relationship

Substances

  • Fluorescent Dyes
  • Indicators and Reagents
  • Receptors, Estrogen
  • Hexestrol
  • Estradiol