Quantitative structure-activity relationships for polychlorinated hydroxybiphenyl estrogen receptor binding affinity: An Assessment of conformer flexibility

Author:

Bradbury Steven P.,Ankley Gerald T.,Mekenyan Ovanes G.

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Environmental Chemistry

Reference35 articles.

1. The specificities of the estrogen receptor of human uterus;Hahnel;J. Steroid Biochem.,1973

2. The molecular structure of 16 α-iodo-17β-estradiol, ahigh affinity ligand for the estrogen receptor;Hochberg;J. Steroid Biochem.,1986

3. Using three-deminisional quantitative structure-activity relationships to examine estrogen receptor binding affinities of polychlorinated hydroxybiphenyls;Waller;Environ. Health Perspect.,1995

4. 2-Arylindenes and 2-arylindenones: Molecular structures and considerations in the binding orientation of unsymmetrical non-steroidal ligands to the estrogen receptor;Anstead;J. Med. Chem.,1989

5. Skeletal conformations and receptor binding of some 9,11-modified estradiols;Palomino;J. Steroid Biochem. Mol. Biol.,1994

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