Molecular aspects of phytoestrogen selective binding at estrogen receptors

被引:113
作者
Turner, Joseph V.
Agatonovic-Kustrin, Snezana
Glass, Beverley D.
机构
[1] Univ Queensland, Sch Med, Rural Clin Div, Toowoomba, Qld 4350, Australia
[2] James Cook Univ, Sch Pharm & Mol Sci, Townsville, Qld, Australia
关键词
hormones; drug design; drug discovery; molecular structure; functional groups; BIOLOGICAL EVALUATION; LIGANDS; ALPHA; AFFINITY; DISCOVERY; AGONISTS; CANCER; SERIES;
D O I
10.1002/jps.20987
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Phytoestrogens are a diverse group of plant-derived compounds that structurally or functionally mimic mammalian estrogens and show potential benefits for human health. An increase in phytoestrogen research over the past few decades has demonstrated the biological complexity of phytoestrogens, which belong to several different chemical classes and act through diverse mechanisms. Identification of the estrogen receptor beta (ER beta) and research into various ligand classes has enabled elucidation of molecular aspects important in selective ER binding. This article explores the structural characteristics and significance of functional groups as they relate to phytoestrogen selectivity for ER binding. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:1879 / 1885
页数:7
相关论文
共 37 条
[1]
Phyto-oestrogens and cancer [J].
Adlercreutz, H .
LANCET ONCOLOGY, 2002, 3 (06) :364-373
[2]
Artificial neural network modeling of phytoestrogen binding to estrogen receptors [J].
Agatonovic-Kustrin, S. ;
Turner, J. V. .
LETTERS IN DRUG DESIGN & DISCOVERY, 2006, 3 (07) :436-442
[3]
The estradiol pharmacophore: Ligand structure-estrogen receptor binding affinity relationships and a model for the receptor binding site [J].
Anstead, GM ;
Carlson, KE ;
Katzenellenbogen, JA .
STEROIDS, 1997, 62 (03) :268-303
[4]
Bakhchinian Robert, 2003, Farmaco (Lausanne), V58, P1201, DOI 10.1016/j.farmac.2003.07.001
[5]
COUMESTROL, A NEW ESTROGEN ISOLATED FROM FORAGE CROPS [J].
BICKOFF, EM ;
BOOTH, AN ;
LYMAN, RL ;
LIVINGSTON, AL ;
THOMPSON, CR ;
DEEDS, F .
SCIENCE, 1957, 126 (3280) :969-970
[6]
Molecular basis of agonism and antagonism in the oestrogen receptor [J].
Brzozowski, AM ;
Pike, ACW ;
Dauter, Z ;
Hubbard, RE ;
Bonn, T ;
Engstrom, O ;
Ohman, L ;
Greene, GL ;
Gustafsson, JA ;
Carlquist, M .
NATURE, 1997, 389 (6652) :753-758
[7]
Cassidy A., 1999, BNF Nutrition Bulletin, V24, P22, DOI 10.1111/j.1467-3010.1999.tb01130.x
[8]
Novel structural templates for estrogen-receptor ligands and prospects for combinatorial synthesis of estrogens [J].
Fink, BE ;
Mortensen, DS ;
Stauffer, SR ;
Aron, ZD ;
Katzenellenbogen, JA .
CHEMISTRY & BIOLOGY, 1999, 6 (04) :205-219
[9]
Quantitative structure-activity relationships for estrogen receptor binding affinity of phenolic chemicals [J].
Hu, JY ;
Aizawa, T .
WATER RESEARCH, 2003, 37 (06) :1213-1222
[10]
Estrogen receptor ligands.: II.: Discovery of benzoxathiins as potent, selective estrogen receptor α modulators [J].
Kim, S ;
Wu, JY ;
Birzin, ET ;
Frisch, K ;
Chan, W ;
Pai, LY ;
Yang, YT ;
Mosley, RT ;
Fitzgerald, PMD ;
Sharma, N ;
Dahllund, J ;
Thorsell, AG ;
DiNinno, F ;
Rohrer, SP ;
Schaeffer, JM ;
Hammond, ML .
JOURNAL OF MEDICINAL CHEMISTRY, 2004, 47 (09) :2171-2175