BAY 1214784

发表于由

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白，专注于信号通路和疾病研究领域。

BAY 1214784 

BAY 1214784 是人促性腺激素释放激素受体 (hGnRH-R) 的有效、选择性和口服活性拮抗剂。BAY 1214784 是螺二氢吲哚衍生物化合物。BAY 1214784 可有效降低血浆促黄体激素水平高达 49%，同时具有较低的药代动力学变异性和良好的耐受性。BAY 1214784 具有研究子宫肌瘤的潜力。

BAY 1214784

BAY 1214784 Chemical Structure

CAS No. : 1631164-25-4

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生物活性

BAY 1214784 is a potent, selective, and orally active antagonist of the human gonadotropin-releasing hormone receptor (hGnRH-R). BAY 1214784 is a spiroindoline derivative compound. BAY 1214784 effectively lowers plasma luteinizing hormone levels by up to 49%, at the same time being associated with low pharmacokinetic variability and good tolerability. BAY 1214784 has the potential for the research of uterine fibroids[1].

分子量

672.11

Formula

C29H26ClF4N3O5S2
CAS 号

1631164-25-4
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献

  • [1]. Panknin O, et al. Discovery and Characterization of BAY 1214784, an Orally Available Spiroindoline Derivative Acting as a Potent and Selective Antagonist of the Human Gonadotropin-Releasing Hormone Receptor as Proven in a First-In-Human Study in Postmenopausal Women. J Med Chem. 2020;63(20):11854-11881

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