17β-Hydroxysteroid dehydrogenase inhibitors: a patent review

被引:73
作者
Poirier, Donald [1 ]
机构
[1] Univ Laval, CHUQ CHUL, Res Ctr, Endocrinol & Genom Unit,Lab Med Chem, Quebec City, PQ G1V 4G2, Canada
基金
加拿大健康研究院;
关键词
17 beta-hydroxysteroid dehydrogenase; androgen; cancer; enzyme; estrogen; inhibitor; steroid; structure-activity relationship; therapy; 4,5-DISUBSTITUTED CIS-PYRROLIDINONES; SELECTIVE NONSTEROIDAL INHIBITORS; IN-SITU HYBRIDIZATION; 17-BETA-HYDROXY STEROID DEHYDROGENASE; BETA-HYDROXYSTEROID DEHYDROGENASES; ESTROGEN-DEPENDENT DISEASES; BREAST-CANCER; BIOLOGICAL EVALUATION; TYPE-1; 17-BETA-HSD1; II; 17-BETA-HYDROXYSTEROID-DEHYDROGENASE;
D O I
10.1517/13543776.2010.505604
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Importance of the field: 17 beta-Hydroxysteroid dehydrogenases (17 beta-HSDs) mainly catalyze the reduction of C17-ketosteroids to their corresponding hydroxylated forms as well as the reverse reaction (oxidation). Able to convert inactive or less active steroid hormones into more potent ones and vice versa, certain 17 beta-HSDs play a key role, especially in the regulation of estrogen and androgen levels. The therapeutic potential of this enzyme family, especially for the treatment of breast cancer, prostate cancer, acne and osteoporosis, then stimulated the development of inhibitors of 17 beta-HSDs and important progress was achieved over the last years. Areas covered in this review: This review article reports all patent applications related to the inhibitors of 17 beta-HSD5, including some articles needed to complement the information presented. What the reader will gain: Readers will be informed about the role and function of 17 beta-HSDs in the first section and about the history of inhibitor development in the second section. Furthermore, in the third and main section, the readers will learn about the structures of patented inhibitors originating from different companies and academic groups. Take home message: The increase in the number of 17 beta-HSD inhibitors reported in the last years augurs well for the future. The challenge is now to translate these results into clinical studies to allow determination of the therapeutic usefulness of 17 beta-HSD inhibitors.
引用
收藏
页码:1123 / 1145
页数:23
相关论文
共 176 条
  • [1] Search for function and modulation of enzyme activity: The international workshop on 11beta and 17beta-hydroxysteroid dehydrogenases, 8-11 May 2005, Elmau Castle, Germany
    Adamski, J
    [J]. MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2006, 248 (1-2) : 1 - 2
  • [2] A guide to 17β-hydroxysteroid dehydrogenases
    Adamski, J
    Jakob, FJ
    [J]. MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2001, 171 (1-2) : 1 - 4
  • [3] Introduction to the workshop on the molecular and cell biology of hydroxysteroid dehydrogenases
    Adamski, J
    deLaunoit, Y
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1995, 55 (5-6) : 445 - 446
  • [4] Pre-receptor steroid metabolism as target for pharmacological treatment
    Adamski, Jerzy
    [J]. MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2009, 301 (1-2) : 1 - 1
  • [5] The role of the heterocycle in bis(hydroxyphenyl)triazoles for inhibition of 17β-Hydroxysteroid Dehydrogenase (17β-HSD) type 1 and type 2
    Al-Soud, Yaseen A.
    Bey, Emmanuel
    Oster, Alexander
    Marchais-Oberwinkler, Sandrine
    Werth, Ruth
    Kruchten, Patricia
    Frotscher, Martin
    Hartmann, Rolf W.
    [J]. MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2009, 301 (1-2) : 212 - 215
  • [6] Novel inhibitors of 17β-hydroxysteroid dehydrogenase type 1:: Templates for design
    Allan, Gillian M.
    Vicker, Nigel
    Lawrence, Harshani R.
    Tutill, Helena J.
    Day, Joanna M.
    Huchet, Marion
    Ferrandis, Eric
    Reed, Michael J.
    Purohit, Atul
    Potter, Barry V. L.
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (08) : 4438 - 4456
  • [7] Novel, potent inhibitors of 17β-hydroxy steroid dehydrogenase type 1
    Allan, GM
    Bubert, C
    Vicker, N
    Smith, A
    Tutill, HJ
    Purohit, A
    Reed, MJ
    Potter, BVL
    [J]. MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2006, 248 (1-2) : 204 - 207
  • [8] Modification of estrone at the 6, 16, and 17 positions:: Novel potent inhibitors of 17β-hydroxysteroid dehydrogenase type 1
    Allan, GM
    Lawrence, HR
    Cornet, J
    Bubert, C
    Fischer, DS
    Vicker, N
    Smith, A
    Tutill, HJ
    Purohit, A
    Day, JM
    Mahon, MF
    Reed, MJ
    Potter, BVL
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2006, 49 (04) : 1325 - 1345
  • [9] [Anonymous], [No title captured], Patent No. 2006125800
  • [10] [Anonymous], [No title captured]