4-[3-(4-hydroxyphenyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile | 915086-59-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑烷类
• 英文名称: 4-[3-(4-hydroxyphenyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile
• 英文别名: 4-[3-(4-Hydroxyphenyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
• CAS: 915086-59-8
• 化学式: C₁₉H₁₄F₃N₃O₃
• 分子量: 389.334
• InChiKey: YAURGAWHOGZLGR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  28
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  84.6
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  4-[3-(4-羟基苯基)-4,4-二甲基-5-氧代-2-硫代咪唑烷-1-基]-2-三氟甲基苯甲腈 在 双氧水 作用下， 以 溶剂黄146 为溶剂， 反应 12.0h， 以87%的产率得到4-[3-(4-hydroxyphenyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile
  参考文献：
  名称：

  WO2006/124118

  摘要：

  公开号：

文献信息

• COMPOUNDS AND METHODS FOR THE TARGETED DEGRADATION OF ANDROGEN RECEPTOR
  申请人：Arvinas, Inc.

  公开号：US20180099940A1

  公开（公告）日：2018-04-12

  The present disclosure relates to bifunctional compounds, which find utility to degrade and (inhibit) Androgen Receptor. In particular, the present disclosure is directed to compounds, which contain on one end a cereblon ligand which binds to the E3 ubiquitin ligase and on the other end a moiety which binds Androgen Receptor, such that Androgen Receptor is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of Androgen Receptor. The present disclosure exhibits a broad range of pharmacological activities associated with compounds according to the present disclosure, consistent with the degradation/inhibition of Androgen Receptor.

  本公开涉及双功能化合物，其用于降解和（抑制）雄激素受体。具体而言，本公开涉及包含一端结合到E3泛素连接酶的谷氨酰腺苷环配体，另一端结合到雄激素受体的部分的化合物，使得雄激素受体与泛素连接酶靠近，以实现雄激素受体的降解（和抑制）。本公开展示了与根据本公开涉及的化合物相关的广泛的药理活性范围，与雄激素受体的降解/抑制一致。
• [EN] COMPOUNDS AND METHODS FOR THE TARGETED DEGRADATION OF THE ANDROGEN RECEPTOR<br/>[FR] COMPOSÉS ET PROCÉDÉS POUR LA DÉGRADATION CIBLÉE DU RÉCEPTEUR DES ANDROGÈNES
  申请人：ARVINAS INC

  公开号：WO2016118666A1

  公开（公告）日：2016-07-28

  The present invention relates to bifunctional compounds, which find utility to degrade and (inhibit) Androgen Receptor. In particular, the present invention is directed to compounds, which contain on one end a VHL ligand which binds to the ubiquitin ligase and on the other end a moiety which binds Androgen Receptor such that Androgen Receptor is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of Androgen Receptor. The present invention exhibits a broad range of pharmacological activities associated with compounds according to the present invention, consistent with the degradation/inhibition of Androgen Receptor.

  本发明涉及双功能化合物，其可用于降解和（抑制）雄激素受体。具体而言，本发明涉及含有一端与泛素连接酶结合的VHL配体，另一端含有与雄激素受体结合的部分的化合物，使得雄激素受体与泛素连接酶靠近以实现雄激素受体的降解（和抑制）。本发明展示了与根据本发明的化合物相关的广泛的药理活性，与雄激素受体的降解/抑制一致。
• DIARYLHYDANTOIN COMPOUNDS AS ANDROGEN RECEPTOR ANTAGONISTS FOR TREATMENT OF CANCER
  申请人：The Regents of the University of California

  公开号：EP3106162A1

  公开（公告）日：2016-12-21

  The present invention relates to a particular diarylhydantoin compound acting by reducing the androgen-receptor(AR) activity. The compound is thus for use in treatment of diseases such as hormone refractory cancer, prostate cancer, benign prostate hyperplasia, breast cancer and ovarian cancer.

  本发明涉及一种特定的二苯基异噁唑酮化合物，通过减少雄激素受体（AR）活性发挥作用。因此，该化合物可用于治疗激素难治性癌症、前列腺癌、良性前列腺增生、乳腺癌和卵巢癌等疾病。
• TREATMENT OF HYPERPROLIFERATIVE DISORDERS WITH DIARYLHYDANTOIN COMPOUNDS
  申请人：Sawyers Charles L.

  公开号：US20120295944A1

  公开（公告）日：2012-11-22

  The present invention relates to diarylhydantoin compounds, including diarylthiohydantoins, and methods for synthesizing them and using them in the treatment of hormone refractory prostate cancer.

  本发明涉及二苯基异噁唑烷酮化合物，包括二苯基硫代异噁唑烷酮，以及合成它们和在治疗荷尔蒙难治性前列腺癌中使用它们的方法。
• DIARYLHYDANTOIN COMPOUNDS
  申请人：The Regents of the University of California

  公开号：US20150112082A1

  公开（公告）日：2015-04-23

  The present invention relates to diarylhydantoin compounds, including diarylthiohydantoins, and methods for synthesizing them and using them in the treatment of hormone refractory prostate cancer.

  本发明涉及二芳基酰脲化合物，包括二芳基硫酰脲，以及合成它们和在治疗激素难治性前列腺癌中使用它们的方法。