1-ethyl-4-phenyl-piperidine-4-carbonitrile | 29600-34-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: 1-ethyl-4-phenyl-piperidine-4-carbonitrile
• 英文别名: 1-Aethyl-4-phenyl-piperidin-4-carbonitril；4-Cyano-1-ethyl-4-phenylpiperidin；1-Ethyl-4-phenylpiperidine-4-carbonitrile
• CAS: 29600-34-8
• 化学式: C₁₄H₁₈N₂
• 分子量: 214.31
• InChiKey: MSPXCURMCDOZIA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  16
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  27
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1-ethyl-4-phenyl-piperidine-4-carbonitrile 在 lithium aluminium tetrahydride 、 乙醚 作用下， 生成 C-(1-ethyl-4-phenyl-[4]piperidyl)-methylamine
  参考文献：
  名称：

  Chiavarelli et al., Gazzetta Chimica Italiana, 1957, vol. 87, p. 427,436

  摘要：

  DOI：
• 作为产物：
  描述：

  二(2-氯乙基)乙胺 、 苯乙腈 在 苯 作用下， 生成 1-ethyl-4-phenyl-piperidine-4-carbonitrile
  参考文献：
  名称：

  Chiavarelli et al., Gazzetta Chimica Italiana, 1957, vol. 87, p. 427,436

  摘要：

  DOI：

文献信息

• LUPEOL-TYPE TRITERPENE DERIVATIVES AS ANTIVIRALS
  申请人：PARTHASARADHI REDDY Bandi

  公开号：US20110015196A1

  公开（公告）日：2011-01-20

  The invention relates to novel lupeol-type triterpene derivatives and related compounds, and pharmaceutical compositions useful for therapeutic treatment of viral diseases and particularly HIV mediated diseases.

  这项发明涉及新型鲁皮醇类三萜衍生物及相关化合物，以及用于治疗病毒性疾病特别是HIV介导疾病的药物组合物。
• Cannabinoid receptor ligands and uses thereof
  申请人：Pfizer Inc.

  公开号：US20040214837A1

  公开（公告）日：2004-10-28

  Compounds of Formula (I) that act as cannabinoid receptor ligands and their uses in the treatment of diseases linked to the mediation of the cannabinoid receptors in animals are described herein. 1

  本文描述了作为大麻素受体配体的化合物（I）及其在治疗与动物体内大麻素受体介导相关疾病中的用途。
• Substituted Piperidines that Increase P53 Activity and the Uses Thereof
  申请人：Ma Yao

  公开号：US20080004287A1

  公开（公告）日：2008-01-03

  In its many embodiments, the present invention discloses novel compounds, as inhibitors of HDM2 protein, methods for preparing such compounds, pharmaceutical compositions including one or more such compounds, methods of treatment, prevention, inhibition, of one or more diseases associated with the HDM2 protein or P53 using such compounds or pharmaceutical compositions.

  在其多种实施形式中，本发明披露了作为HDM2蛋白抑制剂的新型化合物，制备这种化合物的方法，包括一种或多种这种化合物的药物组合物，以及利用这种化合物或药物组合物进行与HDM2蛋白或P53相关的一种或多种疾病的治疗、预防、抑制方法。
• CANNABINOID RECEPTOR LIGANDS AND USES THEREOF
  申请人：Griffith A. David

  公开号：US20070275964A1

  公开（公告）日：2007-11-29

  Compounds of Formula (I) that act as cannabinoid receptor ligands and their uses in the treatment of diseases linked to the mediation of the cannabinoid receptors in animals are described herein.

  本文描述了化学式为(I)的化合物，它们作为大麻素受体配体并在动物中治疗与大麻素受体介导相关的疾病中的用途。
• QUINOLIZIDINONE CARBOXAMIDE M1 RECEPTOR POSITIVE ALLOSTERIC MODULATORS
  申请人：Kuduk Scott D.

  公开号：US20120232076A1

  公开（公告）日：2012-09-13

  The present invention is directed to compounds of formula (I) which are M1 receptor positive allosteric modulators and that are useful in the treatment of diseases in which the M1 receptor is involved, such as Alzheimer's disease, schizophrenia, pain or sleep disorders. The invention is also directed to pharmaceutical compositions comprising the compounds, and to the use of the compounds and compositions in the treatment of diseases mediated by the M1 receptor.

  本发明涉及式(I)的化合物，它们是M1受体正向变构调节剂，并且在治疗M1受体参与的疾病，如阿尔茨海默病、精神分裂症、疼痛或睡眠障碍方面有用。本发明还涉及包含这些化合物的制药组合物，以及使用这些化合物和组合物治疗M1受体介导的疾病。