1-Adamantanamin-4α-ol | 22591-69-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-Adamantanamin-4α-ol
• 英文别名: 1-Aminoadamantan-4-ol；5-amino-adamantan-2-ol；5-Aminoadamantan-2-ol
• CAS: 22591-69-1
• 化学式: C₁₀H₁₇NO
• mdl: MFCD13265361
• 分子量: 167.251
• InChiKey: IQZMKGCMSXOILZ-UHFFFAOYSA-N

物化性质

• 熔点：
  248-250 °C(Solv: ethyl ether (60-29-7))
• 沸点：
  275.6±33.0 °C(Predicted)
• 密度：
  1.205±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.4
• 重原子数：
  12
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  46.2
• 氢给体数：
  2
• 氢受体数：
  2

文献信息

• Aryl sulfonyl piperidines
  申请人：Gillespie Paul

  公开号：US20060199816A1

  公开（公告）日：2006-09-07

  Provided herein are compounds of the formula (1): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of diseases such as, for example, type II diabetes mellitus and metabolic syndrome.

  本文提供了以下式（1）的化合物： 以及其药学上可接受的盐，其中取代基如规范中所披露的那样。这些化合物及含有它们的药物组合物对于治疗诸如II型糖尿病和代谢综合征等疾病是有用的。
• METHODS OF USE OF ANTIVIRAL COMPOUNDS
  申请人：Wang Jizhou

  公开号：US20110065766A1

  公开（公告）日：2011-03-17

  The present invention relates, in part, to methods of treatment, prevention, and inhibition of viral disorders. In one aspect, the present invention relates to inhibition of the M2 proton channel of influenza viruses (e.g. influenza A virus) and other similar viroporins (e.g., VP24 of Ebola and Marburg viruses; and NS3 protein of Bluetongue). The present invention further relates, inter alia, to compounds which have been shown to possess antiviral activity, in particular, inhibiting the M2 proton channel of influenza viruses.

  本发明涉及部分治疗、预防和抑制病毒性疾病的方法。在一个方面，本发明涉及抑制流感病毒（例如流感A病毒）和其他类似的病毒孔蛋白（例如埃博拉和马尔堡病毒的VP24；以及蓝舌病的NS3蛋白）的M2质子通道。本发明还涉及已被证明具有抗病毒活性的化合物，特别是抑制流感病毒M2质子通道的化合物。
• Azaadamantane Ester and Carbamate Derivatives and Methods of Use Thereof
  申请人：Schrimpf Michael R.

  公开号：US20080255178A1

  公开（公告）日：2008-10-16

  The invention relates to compounds that are substituted azaadamantane ester and carbamate derivatives, compositions comprising such compounds, and methods of using such compounds and compositions.

  本发明涉及取代的氮杂莫反烷酯和氨基甲酸酯衍生物化合物，包括含有这些化合物的组合物，以及使用这些化合物和组合物的方法。
• TETRAHYDROQUINOXALINE UERA DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION
  申请人：Braun Alain Jean

  公开号：US20120245148A1

  公开（公告）日：2012-09-27

  The present invention relates to tetrahydroquinoxaline urea derivatives, to their preparation and to their therapeutic application.

  本发明涉及四氢喹喔啉脲衍生物，其制备方法及其治疗应用。
• BI- AND POLYCYCLIC SUBSTITUTED ISOQUINOLINE AND ISOQUINOLINONE DERIVATIVES
  申请人：Plettenburg Oliver

  公开号：US20110190340A1

  公开（公告）日：2011-08-04

  The invention relates to bi- and polycyclic substituted isoquinoline and isoquinolinones of the formula (I) wherein R 1 to R 12 are as defined in the application useful for the treatment and/or prevention of diseases associated with Rho-kinase and/or Rho-kinase mediated phosphorylation of myosin light chain phosphatase, and compositions containing such compounds.

  本发明涉及式（I）的双环和多环取代的异喹啉和异喹啉酮，其中R1至R12如本申请所定义，用于治疗和/或预防与Rho-激酶和/或Rho-激酶介导的肌球蛋白轻链磷酸酶的磷酸化相关的疾病，以及含有这些化合物的组合物。