Benzoxepin-derived estrogen receptor modulators: A novel molecular scaffold for the estrogen receptor

被引:54
作者
Lloyd, DG
Hughes, RB
Zisterer, DM
Williams, DC
Fattorusso, C
Catalanotti, B
Campiani, G
Meegan, MJ [1 ]
机构
[1] Trinity Coll Dublin, Dept Biochem, Dublin 2, Ireland
[2] Trinity Coll Dublin, Sch Pharm, Dublin 2, Ireland
[3] Univ Naples Federico II, Dipartimento Chim Sostanze Nat, I-80131 Naples, Italy
[4] Univ Siena, Dipartimento Farm Chim Tecnol, Fac Farm, I-53100 Siena, Italy
关键词
D O I
10.1021/jm0495834
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
We present and examine the efficacy of a novel benzoxepin-based scaffold for modulation of the human estrogen receptor. Receptor tolerance of this new molecular scaffold is examined through presentation of experimentally determined antiproliferative effects on human MCF-7 breast tumor cells and measured binding affinities. The effect of functional group substitution on the benzoxepin scaffold is explored through a brief computational structure-activity relationship investigation with molecular simulation.
引用
收藏
页码:5612 / 5615
页数:4
相关论文
共 35 条
[1]  
*ACC INC, 2000, DISC MOD INS
[2]   Interaction of steroid hormone receptors with the transcription initiation complex [J].
Beato, M ;
SanchezPacheco, A .
ENDOCRINE REVIEWS, 1996, 17 (06) :587-609
[3]   2-phenylspiroindenes: A novel class of Selective Estrogen Receptor Modulators (SERMs) [J].
Blizzard, TA ;
Morgan, JD ;
Mosley, RT ;
Birzin, ET ;
Frisch, K ;
Rohrer, SP ;
Hammond, ML .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2003, 13 (03) :479-483
[4]   APPLICATION OF THE SUZUKI BIPHENYL SYNTHESIS TO THE NATURAL-PRODUCTS BIPHENOMYCIN AND VANCOMYCIN [J].
BROWN, AG ;
CRIMMIN, MJ ;
EDWARDS, PD .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1992, (01) :123-130
[5]   INCREASING THE NUMBER OF TANDEM ESTROGEN RESPONSE ELEMENTS INCREASES THE ESTROGENIC ACTIVITY OF A TAMOXIFEN ANALOG [J].
CATHERINO, WH ;
JORDAN, VC .
CANCER LETTERS, 1995, 92 (01) :39-47
[6]   Cupric acetate mediated N-arylation by arylboronic acids: A preliminary investigation into the scope of application [J].
Cundy, DJ ;
Forsyth, SA .
TETRAHEDRON LETTERS, 1998, 39 (43) :7979-7982
[7]  
FEISER LF, 1987, REAGENTS ORGANIC CHE, V1, P967
[9]   A new series of estrogen receptor modulators that display selectivity for estrogen receptor β [J].
Henke, BR ;
Consler, TG ;
Go, N ;
Hale, RL ;
Hohman, DR ;
Jones, SA ;
Lu, AT ;
Moore, LB ;
Moore, JT ;
Orband-Miller, LA ;
Robinett, RG ;
Shearin, J ;
Spearing, PK ;
Stewart, EL ;
Turnbull, PS ;
Weaver, SL ;
Williams, SP ;
Wisely, GB ;
Lambert, MH .
JOURNAL OF MEDICINAL CHEMISTRY, 2002, 45 (25) :5492-5505
[10]   Diversity-oriented synthesis of tamoxifen-type tetrasubstituted olefins [J].
Itami, K ;
Kamei, T ;
Yoshida, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (48) :14670-14671