(R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(((tert-butoxycarbonyl)amino)methyl)phenyl)propanoic acid

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: (R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(((tert-butoxycarbonyl)amino)methyl)phenyl)propanoic acid
• 英文别名: (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[4-[[(2-methylpropan-2-yl)oxycarbonylamino]methyl]phenyl]propanoic acid
• 化学式: C₃₀H₃₂N₂O₆
• 分子量: 516.6
• InChiKey: QSPDPKLGXGMDAY-AREMUKBSSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.1
• 重原子数：
  38
• 可旋转键数：
  11
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  114
• 氢给体数：
  3
• 氢受体数：
  6

文献信息

• Substituted indoles and methods of their use
  申请人：Hu Baihua

  公开号：US20070043101A1

  公开（公告）日：2007-02-22

  The present invention relates generally to substituted indoles and methods of using them.

  本发明一般涉及替代吲哚化合物及其使用方法。
• NON-NUCLEOSIDE ANTI-HEPACIVIRUS AGENTS AND USES THEREOF
  申请人：Boyd A. Vincent

  公开号：US20070021434A1

  公开（公告）日：2007-01-25

  The present dislcosure provides amide-based, non-nucleoside compounds having antiviral activity against Hepacivirus, such as hepatitis C virus (HCV), methods and intermediates for synthesizing such compounds, and methods of using the compounds in a variety of contexts, including in the treatment and prevention of viral infections. The present dislcosure also provides methods for identifying amide-based, non-nucleoside compounds having antiviral activity.

  本公开提供了基于酰胺的非核苷类化合物，具有抗Hepacivirus活性，例如丙型肝炎病毒（HCV），合成这类化合物的方法和中间体，以及在各种情境中使用这些化合物的方法，包括在治疗和预防病毒感染中的应用。本公开还提供了识别具有抗病毒活性的基于酰胺的非核苷类化合物的方法。
• COMPOSITIONS AND METHODS FOR TREATING HYPERPROLIFERATIVE DISEASE
  申请人：Cameron Dale Russell

  公开号：US20080171783A1

  公开（公告）日：2008-07-17

  The present disclosure provides amide-based, non-nucleoside compounds having an inhibitory activity against endogenous polymerases, such as polymerase alpha and polymerase gamma. This disclosure further provides uses of treating hyperproliferative diseases or disorders, such as benign or malignant neoplasms, and more specifically cancers that are sensitive to inhibition of polymerase alpha and polymerase gamma.

  本公开提供了基于酰胺的非核苷类化合物，具有对内源聚合酶（如聚合酶α和聚合酶γ）的抑制活性。本公开进一步提供了用于治疗过度增殖性疾病或疾病的用途，例如良性或恶性肿瘤，更具体地是对聚合酶α和聚合酶γ抑制敏感的癌症。
• Substituted Indoles And Methods Of Their Use
  申请人：HU Baihua

  公开号：US20100137363A1

  公开（公告）日：2010-06-03

  The present invention relates generally to substituted indoles and methods of using them.

  本发明涉及替代吲哚及其使用方法。
• Novel materials and methods for the treatment of Alzheimer's disease patients
  申请人：Smith O. Steven

  公开号：US20060062797A1

  公开（公告）日：2006-03-23

  The invention generally relates to the treatment of patients with Alzheimer's disease, at risk for Alzheimer's disease, and other neurodegenerative diseases. More specifically, embodiments of the present invention contemplate novel compositions and methods for the treatment of such patients. In one embodiment, the present invention contemplates proteins and protein variants that function by depolymerizing or preventing the polymerization of amyloid plaques believed to play a role in the etiology of Alzheimer's disease.

  本发明一般涉及阿尔茨海默病患者、有阿尔茨海默病风险的患者以及其他神经退行性疾病患者的治疗。更具体地说，本发明的实施方案考虑了治疗此类患者的新型组合物和方法。在一个实施方案中，本发明考虑了通过解聚或阻止淀粉样蛋白斑块的聚合来发挥作用的蛋白质和蛋白质变体，据信淀粉样蛋白斑块在阿尔茨海默病的病因学中起作用。