4-[[4-(乙酰氧基)苯基]-2-吡啶基甲基]苯酚 | 72901-16-7

• 物质功能分类: 分析化学 - 标准品 - 药典标准品和杂质标准品
• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 4-[[4-(乙酰氧基)苯基]-2-吡啶基甲基]苯酚
• 中文别名: 比沙可啶相关物质C
• 英文名称: Monoacetyl bisacodyl
• 英文别名: [4-[(4-hydroxyphenyl)-pyridin-2-ylmethyl]phenyl] acetate
• CAS: 72901-16-7
• 化学式: C₂₀H₁₇NO₃
• 分子量: 319.4
• InChiKey: IGNJZSFTZVUILA-UHFFFAOYSA-N

物化性质

• 沸点：
  476.1±45.0 °C(Predicted)
• 密度：
  1.219±0.06 g/cm3(Predicted)
• 溶解度：
  可溶于氯仿（少许）、乙酸乙酯（少许）、甲醇（少许）

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  24
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.1
• 拓扑面积：
  59.4
• 氢给体数：
  1
• 氢受体数：
  4

安全信息

• WGK Germany：
  3

文献信息

• Renin Inhibitors
  申请人：Baldwin John J.

  公开号：US20090312369A1

  公开（公告）日：2009-12-17

  The present invention is directed to aspartic protease inhibitors represented by the following structural formula (I), or a pharmaceutically acceptable salt thereof. The present invention is also directed to pharmaceutical compositions comprising the aspartic protease inhibitors of Structural Formula (I). Methods of antagonizing one or more aspartic proteases in a subject in need thereof, and methods for treating an aspartic protease mediated disorder in a subject using these aspartic protease inhibitors are also disclosed.

  本发明涉及以下结构式(I)所表示的天冬氨酸蛋白酶抑制剂，或其药学上可接受的盐。本发明还涉及包括结构式(I)的天冬氨酸蛋白酶抑制剂的制药组合物。本发明还公开了用这些天冬氨酸蛋白酶抑制剂拮抗一个或多个需要治疗的天冬氨酸蛋白酶的方法，以及用这些天冬氨酸蛋白酶抑制剂治疗一个天冬氨酸蛋白酶介导的疾病的方法。
• Renin Inhibitors and Methods of Use Thereof
  申请人：Hammond Marlys

  公开号：US20110160300A1

  公开（公告）日：2011-06-30

  Disclosed are aspartic protease inhibitors represented by the following Formula: wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7a , R 7b and n are as defined herein, or a pharmaceutically acceptable salt thereof, pharmaceutical compositions comprising the same and methods for treating an aspartic protease mediated disorder using the same.

  公开的是以下式子所代表的天冬氨酸蛋白酶抑制剂：其中R1、R2、R3、R4、R5、R6、R7a、R7b和n的定义如本文所述，或其药学上可接受的盐，包括其制备的药物组合物和使用它们治疗天冬氨酸蛋白酶介导的疾病的方法。
• PIPERIDINE RENIN INHIBITORS
  申请人：Baldwin John J.

  公开号：US20120225906A1

  公开（公告）日：2012-09-06

  The present invention is directed to aspartic protease inhibitors represented by the following structural formula: or a pharmaceutically acceptable salt thereof. The present invention is also directed to pharmaceutical compositions comprising the aspartic protease inhibitors of Structural Formula (I). Methods of antagonizing one or more aspartic proteases in a subject in need thereof, and methods for treating an aspartic protease mediated disorder in a subject using these aspartic protease inhibitors are also disclosed.

  本发明涉及以下结构式所表示的天冬氨酸蛋白酶抑制剂或其药学上可接受的盐： 本发明还涉及包含结构式（I）的天冬氨酸蛋白酶抑制剂的制药组合物。还公开了通过使用这些天冬氨酸蛋白酶抑制剂拮抗一个或多个需要的天冬氨酸蛋白酶的方法，以及治疗一个天冬氨酸蛋白酶介导的疾病的方法。
• BISACODYL AND ITS ANALOGUES AS DRUGS FOR USE IN THE TREATMENT OF CANCER
  申请人：Feve Marie

  公开号：US20140186872A1

  公开（公告）日：2014-07-03

  The present invention provides compounds having the formula A: (A) or pharmaceutically acceptable salt thereof, wherein W, R1, R2 and R5 are as defined in classes and subclasses herein, and pharmaceutical compositions thereof, as described generally and in subclasses herein, which compounds are useful as cytotoxic agents towards proliferating and/or quiescent cancer stem cells, and thus are useful, for example, for the treatment of cancer.

  本发明提供了具有以下公式A的化合物：（A）或其药学上可接受的盐，其中W，R1，R2和R5如本类和子类中所定义，并且其制备方法和药物组合物，如本类和子类中所描述。这些化合物可用作对增殖和/或静止的癌细胞干细胞具有细胞毒作用的药物，因此可用于治疗癌症等疾病。
• PROCESS FOR THE PREPARATION OF RENIN INHIBITORS
  申请人：Hammond Marlys

  公开号：US20100311989A1

  公开（公告）日：2010-12-09

  Disclosed is a process for the preparation of tetrahydropyran-di-amine represented by Structural Formula (I): wherein R 1 is H or alkyl and E is H or an amine protecting group.

  公开了一种制备四氢吡喃二胺的方法，其结构式表示为(I)：其中R1为H或烷基，E为H或胺保护基。