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1NDE

Estrogen Receptor beta with Selective Triazine Modulator

1NDE の概要
エントリーDOI10.2210/pdb1nde/pdb
分子名称Estrogen receptor beta, 4-(2-{[4-{[3-(4-CHLOROPHENYL)PROPYL]SULFANYL}-6-(1-PIPERAZINYL)-1,3,5-TRIAZIN-2-YL]AMINO}ETHYL)PHENOL (3 entities in total)
機能のキーワードestrogen receptor, estrogen receptor beta, er, erb, triazine, estrogen, estradiol, oestrogen, transcription
由来する生物種Homo sapiens (human)
細胞内の位置Nucleus : Q92731
タンパク質・核酸の鎖数1
化学式量合計29595.60
構造登録者
主引用文献Henke, B.R.,Consler, T.G.,Go, N.,Hale, R.L.,Hohman, D.R.,Jones, S.A.,Lu, A.T.,Moore, L.B.,Moore, J.T.,Orband-Miller, L.A.,Robinett, R.G.,Shearin, J.,Spearing, P.K.,Stewart, E.L.,Turnbull, P.S.,Weaver, S.L.,Williams, S.P.,Wisely, G.B.,Lambert, M.H.
A New Series of Estrogen Receptor Modulators That Display Selectivity for Estrogen Receptor beta
J.Med.Chem., 45:5492-5505, 2002
Cited by
PubMed Abstract: A series of 1,3,5-triazine-based estrogen receptor (ER) modulators that are modestly selective for the ERbeta subtype are reported. Compound 1, which displayed modest potency and selectivity for ERbeta vs ERalpha, was identified via high-throughput screening utilizing an ERbeta SPA-based binding assay. Subsequent analogue preparation resulted in the identification of compounds such as 21 and 43 that display 25- to 30-fold selectivity for ERbeta with potencies in the 10-30 nM range. These compounds profile as full antagonists at ERbeta and weak partial agonists at ERalpha in a cell-based reporter gene assay. In addition, the X-ray crystal structure of compound 15 complexed with the ligand binding domain of ERbeta has been solved and was utilized in the design of more conformationally restrained analogues such as 31 in an attempt to increase selectivity for the ERbeta subtype.
PubMed: 12459017
DOI: 10.1021/jm020291h
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (3 Å)
構造検証レポート
Validation report summary of 1nde
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-15に公開中

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