6-Tert-butyl-2lambda6-thia-6-azaspiro[3.3]heptane 2,2-dioxide

• 分子结构分类: 有机化合物 - 有机硫化合物 - 磺酰类
• 英文名称: 6-Tert-butyl-2lambda6-thia-6-azaspiro[3.3]heptane 2,2-dioxide
• 英文别名: 6-tert-butyl-2λ6-thia-6-azaspiro[3.3]heptane 2,2-dioxide
• 化学式: C₉H₁₇NO₂S
• 分子量: 203.3
• InChiKey: ZOQNJKTXPDDWOE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.3
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  45.8
• 氢给体数：
  0
• 氢受体数：
  3

文献信息

• 6-AMINOPYRIDIN-3-YL THIAZOLES AS MODULATORS OF RORyT
  申请人：Janssen Pharmaceutica NV

  公开号：US20170313691A1

  公开（公告）日：2017-11-02

  The present invention comprises compounds of Formula I. wherein: A 1 , A 2 , A 3 , A 4 , A 5 , R 1 , and R 2 are defined in the specification. The invention also comprises a method of treating or ameliorating a syndrome, disorder or disease, wherein the syndrome, disorder or disease is rheumatoid arthritis or psoriasis. The invention also comprises a method of modulating RORγt activity in a mammal by administration of a therapeutically effective amount of at least one compound of Formula I.

  本发明涵盖了Formula I的化合物。 其中： A1，A2，A3，A4，A5，R1和R2在说明书中有定义。 该发明还涵盖了一种治疗或改善综合症、疾病或疾病的方法，其中该综合症、疾病为类风湿性关节炎或牛皮癣。该发明还涵盖了通过给哺乳动物施用Formula I中至少一种化合物的治疗有效量来调节RORγt活性的方法。
• TRICYCLIC COMPOUNDS USEFUL AS NEUROGENIC AND NEUROPROTECTIVE AGENTS
  申请人：INCEPTION 1, INC.

  公开号：US20140243313A1

  公开（公告）日：2014-08-28

  The invention disclosed herein is direct to compounds of Formula I and pharmaceutically acceptable salts thereof, which are useful in treating neurodegenerative diseases and promoting the generation or survival of neurons in the mammalian brain. The invention also comprises pharmaceutical compositions comprising a therapeutically effective amount of compound of Formula I or a pharmaceutically acceptable salt thereof. The invention disclosed herein is also directed to a method of promoting the generation or survival of neurons in a patient in need thereof in neurodegenerative and related diseases.

  本发明涉及公式I化合物及其药学上可接受的盐，其在治疗神经退行性疾病和促进哺乳动物大脑中神经元的生成或存活方面有用。本发明还包括含有公式I化合物或其药学上可接受的盐的治疗有效量的药物组合物。本发明还涉及一种在神经退行性和相关疾病患者中促进神经元的生成或存活的方法。
• TRIFLUOROMETHYL ALCOHOLS AS MODULATORS OF RORyt
  申请人：Janssen Pharmaceutica NV

  公开号：US20160122336A1

  公开（公告）日：2016-05-05

  The present invention comprises compounds of Formula I. wherein: X, A 1 , A 2 , A 3 , A 4 , R 1 , R 2 , and R 3 are defined in the specification. The invention also comprises a method of treating or ameliorating a syndrome, disorder or disease, wherein said syndrome, disorder or disease is rheumatoid arthritis or psoriasis. The invention also comprises a method of modulating RORγt activity in a mammal by administration of a therapeutically effective amount of at least one compound of claim 1.

  本发明涉及I式化合物，其中：X，A1，A2，A3，A4，R1，R2和R3在说明书中有定义。本发明还涉及一种治疗或改善综合症、障碍或疾病的方法，其中所述的综合症、障碍或疾病是类风湿性关节炎或银屑病。本发明还涉及一种通过给哺乳动物投予至少一种权利要求1中的化合物的治疗有效量来调节RORγt活性的方法。
• Compounds that inhibit Mcl-1 protein
  申请人：AMGEN INC.

  公开号：US10632128B2

  公开（公告）日：2020-04-28

  Provided herein are myeloid cell leukemia 1 protein (Mcl-1) inhibitors, methods of their preparation, related pharmaceutical compositions, and methods of using the same. For example, provided herein are compounds of Formula I, or a stereoisomer thereof; and pharmaceutically acceptable salts thereof and pharmaceutical compositions containing the compounds. The compounds and compositions provided herein may be used, for example, in the treatment of diseases or conditions, such as cancer.

  本文提供了髓细胞白血病 1 蛋白（Mcl-1）抑制剂、其制备方法、相关药物组合物以及使用方法。例如，本文提供了式 I 的化合物、 或其立体异构体；以及其药学上可接受的盐类和含有这些化合物的药物组合物。本文提供的化合物和组合物可用于治疗癌症等疾病或病症。
• US9187439B2
  申请人：——

  公开号：US9187439B2

  公开（公告）日：2015-11-17