Novel Non-Peptide Antagonists of the GnRH Receptor

GnRH 受体的新型非肽拮抗剂

• 批准号: 6526374
• 负责人: RICHARD SCOTT STRUTHERS
• 金额: $ 47.16万
• 依托单位: NEUROCRINE BIOSCIENCES, INC.
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-04-05 至 2003-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6526374
• 关键词: breast neoplasms; cell line; chemical registry /resource; combinatorial chemistry; drug design /synthesis /production; drug screening /evaluation; endometriosis; gonadotropin releasing factor; hormone inhibitor; hormone receptor; molecular cloning; oral administration; peptide chemical synthesis; pharmacokinetics; prostate neoplasms; receptor expression

DESCRIPTION (provided by applicant): Prostate cancer, breast cancer, endometriosis and uterine fibroids are fairly common and serious diseases in men and women. Their etiology is not fully understood, but all can be treated by removal of endogenous gonadal steroid hormones, testosterone and estrogen. This has led to the discovery of several successful pharmaceutical products based on blocking the actions of the hypothalamic peptide, gonadotropin-releasing hormone (GnRH). Down-regulation of the GnRH receptor by peptide superagonists, or blockade by peptide antagonists, prevents pituitary gonadotropin secretion and leads to dramatic reductions in gonadal steroid production. GnRH-based drugs are now used extensively in these patients, as well as for hormonal manipulation as part of assisted reproductive therapy or for treatment of precocious puberty. Here we propose to develop orally active small molecule antagonists of the GnRH receptor, in order to overcome many of the limitations of these injectable peptide drugs and expand the clinical utility of GnRH-based strategies. In Phase I we have used high-throughput parallel organic synthesis to design multiple chemical series of highly potent, nonpeptide GnRH antagonists. We have also established a series of in vitro and in vivo assays to evaluate absorption, distribution and metabolism of these compounds. In Phase II we propose a combination of parallel synthetic chemistry and assay strategies to optimize pharmacokinetic and pharmacodynamic properties of compounds from three of these series in order to produce compounds suitable for clinical development. PROPOSED COMMERCIAL APPLICATION: NOT AVAILABLE

描述(申请人提供)：前列腺癌、乳腺癌、 子宫内膜异位症和子宫肌瘤在中国是相当常见和严重的疾病。 男人和女人。其病因尚不完全清楚，但均可治疗。 通过清除内源性性腺类固醇激素、睾酮和雌激素。 这导致了几种成功的医药产品的发现 基于阻断下丘脑多肽的作用， 促性腺激素释放激素(GnRH)。促性腺激素释放激素受体的下调 多肽超级激动剂，或被多肽拮抗剂阻断，可预防脑下垂体 促性腺激素分泌并导致性腺类固醇显著减少 制作。以促性腺激素释放激素为基础的药物现在在这些患者中被广泛使用，因为 以及作为辅助生殖治疗一部分的荷尔蒙操作或 用于治疗青春期早熟。在这里，我们建议发展口腔活动 GnRH受体的小分子拮抗剂，以克服许多 这些注射用多肽类药物的局限性及临床推广 基于促性腺激素释放激素的策略的效用。在第一阶段，我们使用了高吞吐量 并行有机合成设计多个化学系列的高效， 非肽类促性腺激素释放激素拮抗剂。我们还建立了一系列的体外和 体内试验评价这些物质的吸收、分布和代谢。 化合物。在第二阶段，我们提出了平行合成化学的组合。 和测试策略，以优化药代动力学和药效学特性 从这些系列中的三种化合物中筛选出合适的化合物 用于临床开发。 建议的商业应用：不可用