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Development of selective estrogen receptor modulator (SERM)-like activity through an indirect mechanism of estrogen receptor antagonism: Defining the binding mode of 7-oxabicyclo 2.2.1 hept-5-ene scaffold core ligands

Academic Article
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Overview

authors

  • Zheng, Y. F.
  • Zhu, M. H.
  • Srinivasan, S.
  • Nwachukwu, J. C.
  • Cavett, V.
  • Min, J.
  • Carlson, K. E.
  • Wang, P. C.
  • Dong, C. N.
  • Katzenellenbogen, J. A.
  • Nettles, Kendall
  • Zhou, H. B.

publication date

  • June 2012

journal

  • ChemMedChem  Journal

subject areas

  • Binding Sites
  • Computer Simulation
  • Crystallography, X-Ray
  • Cycloheptanes
  • Hep G2 Cells
  • Humans
  • Ligands
  • Protein Structure, Tertiary
  • Receptors, Estrogen
  • Selective Estrogen Receptor Modulators
  • Structure-Activity Relationship
  • Transcription, Genetic
  • Transfection
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Research

keywords

  • cycloadditions
  • estrogen
  • estrogen receptors
  • hormones
  • steroids
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Identity

PubMed Central ID

  • PMC4301955

International Standard Serial Number (ISSN)

  • 1860-7179

Digital Object Identifier (DOI)

  • 10.1002/cmdc.201200048

PubMed ID

  • 22517684
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Additional Document Info

start page

  • 1094

end page

  • 1100

volume

  • 7

issue

  • 6

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