Laval University, CHUQ (CHUL)-Research Center, Endocrinology and Genomic Unit, Laboratory of Medicinal Chemistry, 2705 Laurier Boulevard, Québec, Canada.
Expert Opin Ther Pat. 2010 Sep;20(9):1123-45. doi: 10.1517/13543776.2010.505604.
17beta-Hydroxysteroid dehydrogenases (17beta-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 17beta-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 17beta-HSDs and important progress was achieved over the last years.
This review article reports all patent applications related to the inhibitors of 17beta-HSDs, including some articles needed to complement the information presented.
Readers will be informed about the role and function of 17beta-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.
The increase in the number of 17beta-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 17beta-HSD inhibitors.
17β-羟甾脱氢酶(17β-HSD)主要催化 C17-酮甾体转化为相应的羟基化形式以及相反的反应(氧化)。某些 17β-HSD 能够将无活性或活性较低的甾体激素转化为更有效的激素,反之亦然,因此它们在调节雌激素和雄激素水平方面起着关键作用。该酶家族的治疗潜力,特别是在治疗乳腺癌、前列腺癌、痤疮和骨质疏松症方面,刺激了 17β-HSD 抑制剂的开发,并在过去几年取得了重要进展。
本综述文章报道了所有与 17β-HSD 抑制剂相关的专利申请,包括一些需要补充所呈现信息的文章。
读者将在第一节了解 17β-HSD 的作用和功能,在第二节了解抑制剂开发的历史。此外,在第三和主要部分,读者将了解来自不同公司和学术团体的专利抑制剂的结构。
过去几年报道的 17β-HSD 抑制剂数量的增加预示着未来的发展前景良好。现在的挑战是将这些结果转化为临床研究,以确定 17β-HSD 抑制剂的治疗用途。