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Diaryl-substituted salicyl- and anthranyl-ketoximes as potential estrogen receptor ligands

Authors
Journal
Il Farmaco
0014-827X
Publisher
Elsevier
Publication Date
Volume
59
Issue
8
Identifiers
DOI: 10.1016/j.farmac.2004.01.007
Disciplines
  • Biology

Abstract

Abstract 3,4-Diphenylsalicylaldoxime and 3,4-diphenylanthranylaldoxime derivatives, containing small groups (methyl or ethyl) on the imine carbon atom, were synthesized and submitted to biological assays. Binding tests performed on uterine cytosol estrogen receptor (ER) preparation and on purified full-length human ERα and ERβ, showed that the newly synthesised compounds exhibit considerably lower binding affinities with respect to reference non-substituted 3,4-salicylaldoxime.

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